Find link

language:

Find link is a tool written by Edward Betts.

Longer titles found: Neurogenetics (journal) (view), Journal of Neurogenetics (view)

searching for Neurogenetics 203 found (281 total)

Obaid Siddiqi (1,501 words) [view diff] exact match in snippet view article find links to article

Sciences. He made seminal contributions to the field of behavioural neurogenetics using the genetics and neurobiology of Drosophila. Obaid Siddiqi was

National Centre for Biological Sciences (612 words) [view diff] exact match in snippet view article find links to article

of NCBS. He made seminal contributions to the field of behavioural neurogenetics using the genetics and neurobiology of Drosophila. NCBS focuses on fundamental

Max Planck Institute for Experimental Medicine (628 words) [view diff] exact match in snippet view article find links to article

neuroscience: its research activities were organized into the Department of Neurogenetics, the Department of Molecular Neurobiology, and the Department of Molecular

Gene (journal) (271 words) [view diff] exact match in snippet view article

organized into topics, which include Human Genetics, Cancer Genetics, Neurogenetics, Animal Genetics, Genome Editing, Molecular Ecology, Plant Genetics

David C. Rubinsztein (1,277 words) [view diff] exact match in snippet view article find links to article

Cambridge Institute of Medical Research (CIMR), Professor of Molecular Neurogenetics at the University of Cambridge and a UK Dementia Research Institute

Jeffrey C. Hall (2,075 words) [view diff] exact match in snippet view article find links to article

years in Benzer's laboratory. This work triggered his interest in the neurogenetics of Drosophila courtship and led him to the subsequent career path of

Andrew Singleton (1,019 words) [view diff] exact match in snippet view article find links to article

Genetics unit within the Laboratory of Neurogenetics. In 2006 he took over as Chief of the Laboratory of Neurogenetics and became an NIH Distinguished Investigator

Anita Harding (606 words) [view diff] exact match in snippet view article find links to article

United States to learn the burgeoning field of neurogenetics. In 1985 she established the first neurogenetics research group in the United Kingdom at the

Leslie B. Vosshall (1,395 words) [view diff] exact match in snippet view article find links to article

Institute (HHMI) investigator and the Robin Chemers Neustein Professor of Neurogenetics and Behavior at The Rockefeller University. In 2022 she was appointed

Neurosecurity (554 words) [view diff] exact match in snippet view article find links to article

the use of neurotechnologies (such as neuroimaging, neurofeedback, neurogenetics, and neuro-computational data banks) in medicine, the social sphere

Martin Heisenberg (852 words) [view diff] exact match in snippet view article find links to article

at the University of Würzburg. Heisenberg's work has focused on the neurogenetics of Drosophila (the fruit fly), with the aim of investigating the genetic

Elsdon Storey (184 words) [view diff] exact match in snippet view article find links to article

Neurology at Monash University. His clinical and research interests are in neurogenetics (especially the hereditary ataxias) and behavioural neurology (especially

Ellen Sidransky (475 words) [view diff] exact match in snippet view article find links to article

National Human Genome Research Institute. She is chief of the Molecular Neurogenetics Section. Sidransky graduated magna cum laude from Brandeis University

Cause of obsessive–compulsive disorder (3,408 words) [view diff] exact match in snippet view article find links to article

made in the fields of neuroanatomy, neurochemistry, neuroimmunology, neurogenetics, and neuroethology. Many different types of medication can create/induce

GJC2 (714 words) [view diff] exact match in snippet view article find links to article

deletion in the GJA12 gene causes Pelizaeus-Merzbacher-like disease". Neurogenetics. 8 (1): 57–60. doi:10.1007/s10048-006-0065-x. PMID 17031678. S2CID 37200249

Silvia Paracchini (429 words) [view diff] exact match in snippet view article find links to article

Silvia Paracchini FRSE is a Professor of Neurogenetics and Genomics at the University of St Andrews. Her research focuses on the genetics of neurodevelopmental

Christopher Shaw (neurologist) (479 words) [view diff] exact match in snippet view article

FRCP (Hon), FMedSci, FANA (born 1960) is Professor of Neurology and Neurogenetics at the Institute of Psychiatry, Psychology and Neuroscience, King's

Christine Klein (591 words) [view diff] exact match in snippet view article find links to article

Christine Klein is a German physician who is a professor of neurology and neurogenetics at the University of Lübeck. Her research considers the molecular genetics

Drosophilist (263 words) [view diff] exact match in snippet view article find links to article

the fruit fly Drosophila melanogaster to study genetics, development, neurogenetics, behavior and a host of other subjects in animal biology. The core members

James F. Gusella (853 words) [view diff] exact match in snippet view article find links to article

neurodegenerative diseases in humans. He is the Bullard Professor of Neurogenetics in the Department of Genetics at Harvard Medical School and an investigator

Dimitri Krainc (1,333 words) [view diff] exact match in snippet view article find links to article

Feinberg Neuroscience Institute and the Simpson Querrey Center for Neurogenetics at Northwestern University Feinberg School of Medicine. After completing

Elliot S. Gershon (157 words) [view diff] exact match in snippet view article find links to article

department of psychiatry from 1998 to 2004, and chief of the Clinical Neurogenetics branch of the NIMH. He held a NARSAD distinguished investigator grant

Louis Ptáček (1,413 words) [view diff] exact match in snippet view article find links to article

Ptáček is a neurology professor and a director of the Division of Neurogenetics[citation needed] in University of California, San Francisco, School

Thomas Espeseth (77 words) [view diff] exact match in snippet view article find links to article

Professor of Psychology at the University of Oslo. He researches cognitive neurogenetics, such as genetic effects on the brains's morphology, physiology, and

American Journal of Medical Genetics (274 words) [view diff] exact match in snippet view article find links to article

phenotypically driven analyses of disorders of morphogenesis, metabolism, and neurogenetics, especially intellectual disability and related neurodevelopmental conditions

Joe Z. Tsien (2,946 words) [view diff] exact match in snippet view article find links to article

Joe Z. Tsien（钱卓） is a neuroscientist who pioneered Cre/lox-neurogenetics in the mid-1990s, a versatile toolbox for neuroscientists to study the complex

Andrea Gropman (262 words) [view diff] exact match in snippet view article find links to article

pediatric neurologist specializing in neurodevelopmental disabilities and neurogenetics. She is a professor of pediatrics and neurology at the George Washington

Douglas Wahlsten (612 words) [view diff] exact match in snippet view article find links to article

authored acclaimed books on mouse behavior testing and human behavioral neurogenetics. "Psychology Emeriti". University of Alberta. Retrieved 2018-06-06.

Spinal muscular atrophy with lower extremity predominance 1 (339 words) [view diff] exact match in snippet view article find links to article

dominant spinal muscular atrophy with lower extremity predominance". Neurogenetics. 13 (4): 327–332. doi:10.1007/s10048-012-0337-6. PMID 22847149. S2CID 254112503

Hugo Moser (scientist) (1,239 words) [view diff] exact match in snippet view article

(1924–2007) was a Swiss-born American research scientist and director of the Neurogenetics Research Center at the Kennedy Krieger Institute. Moser was also University

ASAH2C (333 words) [view diff] exact match in snippet view article find links to article

segmental duplication shows perturbed expression in Alzheimer's disease". Neurogenetics. 8 (2): 111–20. doi:10.1007/s10048-007-0081-5. PMID 17334805. S2CID 20156514

MYH13 (395 words) [view diff] exact match in snippet view article find links to article

Alzheimer's disease case-control associations using family-based methods". Neurogenetics. 10 (1): 19–25. doi:10.1007/s10048-008-0151-3. PMC 2841132. PMID 18830724

MT-TT (671 words) [view diff] exact match in snippet view article find links to article

mitochondrial tRNA genes in histologically confirmed Parkinson disease". Neurogenetics. 2 (2): 121–7. doi:10.1007/s100480050063. PMID 10369889. S2CID 13031885

Stanley Center for Psychiatric Research at Broad Institute (984 words) [view diff] exact match in snippet view article find links to article

doi: 10.1038/nature13595. McCarroll SA, Feng G, Hyman SE. Genome-scale neurogenetics: Methodology and meaning. Nat Neurosci. 2014 Jun;17(6):756-63. doi:

Philip L. De Jager (237 words) [view diff] exact match in snippet view article find links to article

molecular biophysics and biochemistry from Yale University, a Ph.D in neurogenetics from Rockefeller University, and an MD from Cornell University Medical

RO4491533 (200 words) [view diff] exact match in snippet view article find links to article

negative allosteric modulator in rodent models of depression". Journal of Neurogenetics. 25 (4): 152–66. doi:10.3109/01677063.2011.627485. PMID 22091727. S2CID 207440972

EGR2 (2,066 words) [view diff] exact match in snippet view article find links to article

"EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy". Neurogenetics. 3 (3): 153–7. doi:10.1007/s100480100107. PMID 11523566. S2CID 32746701

NAS Award in the Neurosciences (442 words) [view diff] exact match in snippet view article find links to article

Seymour Benzer (2001) For his pioneering contributions which have brought neurogenetics to maturity. Benzer's discoveries in fruit flies have identified specific

ASAH2B (201 words) [view diff] exact match in snippet view article find links to article

segmental duplication shows perturbed expression in Alzheimer's disease". Neurogenetics. 8 (2): 111–20. doi:10.1007/s10048-007-0081-5. PMID 17334805. S2CID 20156514

Gruber Prize in Neuroscience (367 words) [view diff] exact match in snippet view article find links to article

Neuroscience at University College London 2009 Jeffrey C. Hall, professor of neurogenetics at the University of Maine; Michael Rosbash, professor and director

Rockefeller University (3,222 words) [view diff] exact match in snippet view article find links to article

and psychoanalysis. Erich Jarvis, HHMI Investigator and head of the Neurogenetics of Language Laboratory at Rockefeller University. Seth Lloyd, physicist

Dystonia (3,522 words) [view diff] exact match in snippet view article find links to article

recessive primary torsion dystonia (DYT17) maps to 20p11.22-q13.12". Neurogenetics. 9 (4): 287–293. doi:10.1007/s10048-008-0142-4. PMID 18688663. S2CID 20343435

Dejerine–Sottas disease (666 words) [view diff] exact match in snippet view article find links to article

"EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy". Neurogenetics. 3 (3): 153–7. doi:10.1007/s100480100107. PMID 11523566. S2CID 32746701

ALDH16A1 (392 words) [view diff] exact match in snippet view article find links to article

protein ACP33/maspardin with the aldehyde dehydrogenase ALDH16A1". Neurogenetics. 10 (3): 217–28. doi:10.1007/s10048-009-0172-6. PMC 5585778. PMID 19184135

DNM2 (1,264 words) [view diff] exact match in snippet view article find links to article

dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432". Neurogenetics. 4 (2): 83–5. doi:10.1007/s10048-002-0139-3. PMID 12481986. S2CID 19120964

CDKL5 (2,565 words) [view diff] exact match in snippet view article find links to article

the CDKL5 gene, predicted effects and associated phenotypes" (PDF). Neurogenetics. 10 (3): 241–50. doi:10.1007/s10048-009-0177-1. hdl:2434/70585. PMID 19241098

Torsin A (910 words) [view diff] exact match in snippet view article find links to article

(GAG) deletion in the DYT1 gene with a unique clinical presentation". Neurogenetics. 2 (3): 189–90. doi:10.1007/s100480050082. PMID 10541594. S2CID 27834129

ASAH2 (687 words) [view diff] exact match in snippet view article find links to article

segmental duplication shows perturbed expression in Alzheimer's disease". Neurogenetics. 8 (2): 111–20. doi:10.1007/s10048-007-0081-5. PMID 17334805. S2CID 20156514

Human Phenotype Ontology (307 words) [view diff] exact match in snippet view article find links to article

Robinson PN (September 2012). "Ontological phenotype standards for neurogenetics". Human Mutation. 33 (9): 1333–9. doi:10.1002/humu.22112. PMID 22573485

MFSD8 (708 words) [view diff] exact match in snippet view article find links to article

in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosis". Neurogenetics. 10 (1): 73–7. doi:10.1007/s10048-008-0153-1. PMID 18850119. S2CID 22802019

Karl Deisseroth (2,885 words) [view diff] exact match in snippet view article find links to article

to specific cells in behaving animals by taking advantage of Cre-lox neurogenetics developed by Joe Tsien in the 1990s. Other awards: Deisseroth's 2018

Mucolipidosis type IV (946 words) [view diff] exact match in snippet view article find links to article

O. W.; Slaugenhaupt, S. A.; Goldin, E.; Schiffmann, R. (2002). "The neurogenetics of mucolipidosis type IV". Neurology. 59 (3): 306–13. doi:10.1212/wnl

Sepiapterin reductase deficiency (1,709 words) [view diff] exact match in snippet view article find links to article

deficiency. A splicing defect accounts for a new phenotypic variant. Neurogenetics, 12(3), 183-191. doi: 10.1007/s10048-011-0279-4. Lohmann, E., Koroglu

Sodium- and chloride-dependent creatine transporter 1 (828 words) [view diff] exact match in snippet view article find links to article

clinical description of a patient with a novel SLC6A8 gene mutation". Neurogenetics. 6 (3): 165–8. doi:10.1007/s10048-005-0002-4. PMID 16086185. S2CID 3045047

GABBR1 (1,239 words) [view diff] exact match in snippet view article find links to article

evaluation of its involvement in idiopathic generalized epilepsy". Neurogenetics. 2 (1): 47–54. doi:10.1007/s100480050051. PMID 9933300. S2CID 9649940

Congenital distal spinal muscular atrophy (937 words) [view diff] exact match in snippet view article find links to article

mutations in children with congenital distal spinal muscular atrophy". Neurogenetics. 13 (3): 195–203. doi:10.1007/s10048-012-0328-7. PMID 22526352. S2CID 14428057

Distal myopathy (903 words) [view diff] exact match in snippet view article find links to article

2p13 positions the new candidate region telomeric of the DYSF locus". Neurogenetics. 4 (4): 173–7. doi:10.1007/s10048-003-0154-z. PMID 12836053. S2CID 27539044

Habit reversal training (1,004 words) [view diff] exact match in snippet view article find links to article

MW, Pittenger C (2018). "Tourette disorder and other tic disorders". Neurogenetics, Part I (Review). Handbook of Clinical Neurology. Vol. 147. pp. 343–54

Kir2.1 (1,491 words) [view diff] exact match in snippet view article find links to article

in the KCNJ2 gene has also been shown to cause short QT syndrome. In neurogenetics, Kir2.1 is used in Drosophila research to inhibit neurons, as overexpression

Tripeptidyl peptidase I (1,569 words) [view diff] exact match in snippet view article find links to article

two genes underlying late-infantile neuronal ceroid lipofuscinosis". Neurogenetics. 1 (3): 217–22. doi:10.1007/s100480050032. PMID 10737126. S2CID 23303630

Anion exchange protein 3 (847 words) [view diff] exact match in snippet view article find links to article

exchanger 3 and its potential role in hereditary neurological disease". Neurogenetics. 1 (4): 289–92. doi:10.1007/s100480050043. PMID 10732805. S2CID 22195848

SGCE (908 words) [view diff] exact match in snippet view article find links to article

"Epsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndrome". Neurogenetics. 6 (1): 55–6. doi:10.1007/s10048-004-0206-z. PMID 15627203. S2CID 10589152

Chinnery (141 words) [view diff] exact match in snippet view article find links to article

(1876–1916), English cricketer Patrick Chinnery (born 1968), professor of neurogenetics at the University of Cambridge Sarah Chinnery (1887–1970), British-Australian

Marla Sokolowski (1,194 words) [view diff] exact match in snippet view article find links to article

financial, educational and emotional interventions. In 2021, the Journal of Neurogenetics published and issue in honor of her. The Weston Fellow, Canadian Institute

KIF5A (990 words) [view diff] exact match in snippet view article find links to article

in KIF5A can also cause adult-onset hereditary spastic paraplegia". Neurogenetics. 7 (1): 47–50. doi:10.1007/s10048-005-0027-8. PMID 16489470. S2CID 24405076

KIF5A (990 words) [view diff] exact match in snippet view article find links to article

in KIF5A can also cause adult-onset hereditary spastic paraplegia". Neurogenetics. 7 (1): 47–50. doi:10.1007/s10048-005-0027-8. PMID 16489470. S2CID 24405076

Dystonin (1,478 words) [view diff] exact match in snippet view article find links to article

(September–December 2023). "The DST gene in neurobiology". Journal of Neurogenetics. 37 (4): 131–8. doi:10.1080/01677063.2024.2319880. PMID 38465459. Lynch-Godrei

Dyslexia (8,684 words) [view diff] exact match in snippet view article find links to article

original on 9 January 2017. Benitez A (November 2010). "Neurobiology and neurogenetics of dyslexia". Neurology (In Spanish). 25 (9): 563–81. doi:10.1016/j

Wolf Prize in Medicine (216 words) [view diff] exact match in snippet view article find links to article

Benzer United States for having generated a new field of molecular neurogenetics by his pioneering research on the dissection of the nervous system and

Dysmorphic feature (800 words) [view diff] exact match in snippet view article find links to article

-P.; De Ravel, T. D. (2002). "London Dysmorphology Database, London Neurogenetics Database and Dysmorphology Photo Library on CD-ROM \Version 3] 2001"

Delta-sarcoglycan (1,302 words) [view diff] exact match in snippet view article find links to article

cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2)". Neurogenetics. 1 (1): 49–58. doi:10.1007/s100480050008. PMID 10735275. S2CID 22739920

Dystrobrevin alpha (1,107 words) [view diff] exact match in snippet view article find links to article

Kunkel LM (2000). "The genomic organization of human dystrobrevin". Neurogenetics. 1 (1): 37–42. doi:10.1007/s100480050006. PMID 10735273. S2CID 22588879

John Hardy (geneticist) (1,043 words) [view diff] exact match in snippet view article

Institute on Aging, Bethesda, Maryland, as Chief of the Laboratory of Neurogenetics in 2001. In 2007 he took up the Chair of Molecular Biology of Neurological

SPRED3 (334 words) [view diff] exact match in snippet view article find links to article

"Mutation analysis of CBL-C and SPRED3 on 19q in human glioblastoma". Neurogenetics. 5 (1): 81–2. doi:10.1007/s10048-003-0164-x. PMID 14618415. S2CID 35025882

Downregulation and upregulation (2,178 words) [view diff] exact match in snippet view article find links to article

2016-11-20. Walker DM, Nestler EJ (2018). "Neuroepigenetics and addiction". Neurogenetics, Part II. Handbook of Clinical Neurology. Vol. 148. pp. 747–765. doi:10

List of Max Planck Institutes (277 words) [view diff] exact match in snippet view article find links to article

neuroscience, structural biology, cell biology Max Planck Research Unit for Neurogenetics Frankfurt genetics, medicine, neuroscience, cell biology Social Neuroscience

National Human Genome Research Institute (1,144 words) [view diff] exact match in snippet view article find links to article

Functional Genomics Branch Ellen Sidransky, chief of the Molecular Neurogenetics Section Tara Matise, Head of Computational Genetics at Rutgers University

CMTX3 (173 words) [view diff] exact match in snippet view article find links to article

the X-linked Charcot-Marie-Tooth (CMTX3) locus to a 2.5 Mb region". Neurogenetics. 9 (3): 191–5. doi:10.1007/s10048-008-0126-4. PMC 6852654. PMID 18458969

ALS2 (905 words) [view diff] exact match in snippet view article find links to article

familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33". Neurogenetics. 2 (1): 34–42. doi:10.1007/s100480050049. PMID 9933298. S2CID 33368578

PLEKHG4 (644 words) [view diff] exact match in snippet view article find links to article

autosomal dominant cerebellar ataxia type III in Japanese families". Neurogenetics. 5 (4): 215–21. doi:10.1007/s10048-004-0194-z. PMID 15455264. S2CID 34569635

Richard Smeyne (606 words) [view diff] exact match in snippet view article find links to article

and TrkC. In 1994, Dr. Smeyne left BMS and was named the Head of the Neurogenetics Program in the Division of CNS Research at Hoffmann-La Roche. In 1996

Tourette syndrome (14,863 words) [view diff] exact match in snippet view article find links to article

MW, Pittenger C (2018). "Tourette disorder and other tic disorders". Neurogenetics, Part I (Review). Handbook of Clinical Neurology. Vol. 147. pp. 343–354

Acidic repeat-containing protein (110 words) [view diff] exact match in snippet view article find links to article

maps to DYT3 (dystonia parkinsonism) critical interval in xq13.1". Neurogenetics. 3 (4): 207–13. doi:10.1007/s100480100120. PMID 11714101. S2CID 6872713

Neuromorphology (2,037 words) [view diff] exact match in snippet view article find links to article

(2009). "From Form to Function: the ways to know a neuron". Journal of Neurogenetics. 23 (1–2): 68–77. doi:10.1080/01677060802610604. PMID 19132600. S2CID 14625965

Familial hemiplegic migraine (4,222 words) [view diff] exact match in snippet view article find links to article

causes familial hemiplegic migraine type 2 with cerebellar signs". Neurogenetics. 5 (3): 177–85. doi:10.1007/s10048-004-0183-2. PMID 15459825. S2CID 1480291

NAB1 (573 words) [view diff] exact match in snippet view article find links to article

corepressor proteins, NAB1 and NAB2, in human peripheral neuropathies". Neurogenetics. 4 (1): 37–41. doi:10.1007/s10048-001-0124-2. PMID 12030330. S2CID 1928229

Sepiapterin reductase (1,348 words) [view diff] exact match in snippet view article find links to article

sepiapterin reductase gene (SPR) in a patient with dopa-responsive dystonia". Neurogenetics. 5 (3): 187–190. doi:10.1007/s10048-004-0182-3. PMID 15241655. S2CID 4833737

OMG (gene) (604 words) [view diff] exact match in snippet view article

OMG genes in patients with non-syndromic mental retardation" (PDF). Neurogenetics. 7 (1): 59–66. doi:10.1007/s10048-005-0026-9. hdl:2434/10108. PMID 16425041

Proteolipid protein 1 (1,166 words) [view diff] exact match in snippet view article find links to article

disorders: Pelizaeus-Merzbacher disease and spastic paraplegia type 2". Neurogenetics. 6 (1): 1–16. doi:10.1007/s10048-004-0207-y. PMID 15627202. S2CID 32631043

GABRA4 (780 words) [view diff] exact match in snippet view article find links to article

autism and GABA receptor subunit genes in multiple ethnic groups". Neurogenetics. 7 (3): 167–174. doi:10.1007/s10048-006-0045-1. PMC 1513515. PMID 16770606

Kv1.1 (2,127 words) [view diff] exact match in snippet view article find links to article

a novel potassium channel (KCNA1) mutation in hereditary myokymia". Neurogenetics. 8 (2): 131–5. doi:10.1007/s10048-006-0071-z. PMC 1820748. PMID 17136396

Nektarios Tavernarakis (4,093 words) [view diff] exact match in snippet view article find links to article

Institute of Molecular Biology and Biotechnology, where he is heading the Neurogenetics and Ageing laboratory. He was elected Vice President of the European

Metabotropic glutamate receptor 2 (2,647 words) [view diff] exact match in snippet view article find links to article

negative allosteric modulator in rodent models of depression". Journal of Neurogenetics. 25 (4): 152–66. doi:10.3109/01677063.2011.627485. PMID 22091727. S2CID 207440972

Atlastin-1 (848 words) [view diff] exact match in snippet view article find links to article

autosomal dominant spastic paraplegia caused by novel mutations in SPG3A". Neurogenetics. 5 (4): 239–43. doi:10.1007/s10048-004-0191-2. PMID 15517445. S2CID 21989057

NIPA1 (671 words) [view diff] exact match in snippet view article find links to article

with a pure form of autosomal dominant hereditary spastic paraplegia". Neurogenetics. 6 (2): 79–84. doi:10.1007/s10048-004-0209-9. PMID 15711826. S2CID 2236413

Metabotropic glutamate receptor 3 (3,074 words) [view diff] exact match in snippet view article find links to article

of the human metabotropic glutamate receptor subtype 3". Journal of Neurogenetics. 14 (4): 207–25, 271. doi:10.3109/01677060009084499. PMID 11342382.

Max Planck Institute for Brain Research (1,469 words) [view diff] exact match in snippet view article find links to article

2013), several core facilities, and the Max Planck Research Unit for Neurogenetics of Peter Mombaerts. As of 2016[update], Moritz Helmstaedter is the Managing

VPS13A (676 words) [view diff] exact match in snippet view article find links to article

founder mutation in French Canadian families with chorea-acanthocytosis". Neurogenetics. 6 (3): 151–8. doi:10.1007/s10048-005-0220-9. PMID 15918062. S2CID 10875246

Max Planck Institute for Brain Research (1,469 words) [view diff] exact match in snippet view article find links to article

2013), several core facilities, and the Max Planck Research Unit for Neurogenetics of Peter Mombaerts. As of 2016[update], Moritz Helmstaedter is the Managing

GPR56 (3,019 words) [view diff] exact match in snippet view article find links to article

GPR56 mutations: further delineation of a cobblestone-like phenotype". Neurogenetics. 14 (1): 77–83. doi:10.1007/s10048-012-0352-7. PMID 23274687. S2CID 18696428

VPS13A (676 words) [view diff] exact match in snippet view article find links to article

founder mutation in French Canadian families with chorea-acanthocytosis". Neurogenetics. 6 (3): 151–8. doi:10.1007/s10048-005-0220-9. PMID 15918062. S2CID 10875246

Max Planck Institute of Biophysics (1,067 words) [view diff] exact match in snippet view article find links to article

since 2013) Molecular Sociology (Martin Beck, since 2019) Molecular Neurogenetics (Peter Mombaerts, from 2006 until 2010) A prerequisite for the understanding

Howard Nash (223 words) [view diff] exact match in snippet view article find links to article

(23 August 2011). ""Entitlement, No! Gratitude, Yes!"". Journal of Neurogenetics. 25 (3): 63–77. doi:10.3109/01677063.2011.608137. Insel, Thomas (14

LINGO2 (353 words) [view diff] exact match in snippet view article find links to article

variants are associated with essential tremor and Parkinson disease". Neurogenetics. 11 (4): 401–408. doi:10.1007/s10048-010-0241-x. PMC 3930084. PMID 20369371

Command neuron (829 words) [view diff] exact match in snippet view article find links to article

logic in the field of biology, especially neuroscience". Journal of Neurogenetics. 32 (2): 52–64. doi:10.1080/01677063.2018.1468443. PMC 6510664. PMID 29757057

Dopamine beta-hydroxylase (2,543 words) [view diff] exact match in snippet view article find links to article

gene providing new insights into its structure-function relationship". Neurogenetics. 18 (3): 155–168. doi:10.1007/s10048-017-0519-3. PMID 28707163. S2CID 5259134

Frataxin (2,715 words) [view diff] exact match in snippet view article find links to article

Friedreich ataxia with the site of point mutations in the FRDA gene". Neurogenetics. 1 (4): 253–7. doi:10.1007/s100480050037. PMID 10732799. S2CID 7463903

Gaiti Hasan (837 words) [view diff] exact match in snippet view article find links to article

Complementation of Drosophila itpr Mutants by RatItpr1". Journal of Neurogenetics. 26 (3–4): 328–37. doi:10.3109/01677063.2012.697501. PMID 22817477.

SELENON (884 words) [view diff] exact match in snippet view article find links to article

dystrophy type 1 caused by novel mutations of selenoprotein N gene". Neurogenetics. 7 (3): 175–83. doi:10.1007/s10048-006-0046-0. PMID 16779558. S2CID 25169543

ZFYVE26 (701 words) [view diff] exact match in snippet view article find links to article

interval and phenotypic heterogeneity in three large Arab families". Neurogenetics. 8 (4): 307–15. doi:10.1007/s10048-007-0097-x. PMID 17661097. S2CID 25209385

James Q. Miller (516 words) [view diff] exact match in snippet view article find links to article

eponym Miller–Dieker syndrome. Although his main early interests were in neurogenetics and inflammatory diseases of the nervous system, he maintained activities

NAB2 (850 words) [view diff] exact match in snippet view article find links to article

corepressor proteins, NAB1 and NAB2, in human peripheral neuropathies". Neurogenetics. 4 (1): 37–41. doi:10.1007/s10048-001-0124-2. PMID 12030330. S2CID 1928229

Metabotropic glutamate receptor (3,629 words) [view diff] exact match in snippet view article find links to article

negative allosteric modulator in rodent models of depression". Journal of Neurogenetics. 25 (4): 152–66. doi:10.3109/01677063.2011.627485. PMID 22091727. S2CID 207440972

Yadin Dudai (762 words) [view diff] exact match in snippet view article find links to article

learning and memory, he is also one of the founders of the field of neurogenetics of behavioural plasticity when he was in the group of Seymour Benzer

European Archives of Psychiatry and Clinical Neuroscience (306 words) [view diff] exact match in snippet view article find links to article

(neuropathology, neurophysiology, neurochemistry, neuropsychology, neuroimaging, neurogenetics, molecular biology, animal models). European Archives of Psychiatry

Cereblon (1,350 words) [view diff] exact match in snippet view article find links to article

nonsyndromal mental retardation due to a cereblon p.R419X mutation". Neurogenetics. 9 (3): 219–23. doi:10.1007/s10048-008-0128-2. PMID 18414909. S2CID 20729122

Sacsin (967 words) [view diff] exact match in snippet view article find links to article

spastic ataxia of Charlevoix-Saguenay (ARSACS) families from Turkey". Neurogenetics. 5 (3): 165–70. doi:10.1007/s10048-004-0179-y. PMID 15156359. S2CID 13187102

Causes and origins of Tourette syndrome (2,352 words) [view diff] exact match in snippet view article find links to article

In Daniel H. Geschwind, Henry L. Paulson, Christine Klein (eds.). Neurogenetics, Part I (Review). Handbook of Clinical Neurology. Vol. 147. Elsevier

Mycophenolic acid (3,531 words) [view diff] exact match in snippet view article find links to article

Nguyen KV, et al. (May 2014). "Genotype-phenotype correlations in neurogenetics: Lesch-Nyhan disease as a model disorder". Brain. 137 (Pt 5): 1282–303

Dysferlin (3,492 words) [view diff] exact match in snippet view article find links to article

2p13 positions the new candidate region telomeric of the DYSF locus". Neurogenetics. 4 (4): 173–7. doi:10.1007/s10048-003-0154-z. PMID 12836053. S2CID 27539044

Laboratory mouse (5,999 words) [view diff] exact match in snippet view article find links to article

PMID 31133439. Saul, M. C.; Philip, V. M.; Reinholdt, L. G.; Center for Systems Neurogenetics of Addiction; Chesler, E. J. (2019). "High-diversity mouse populations

Benign familial neonatal seizures (2,574 words) [view diff] exact match in snippet view article find links to article

a large pedigree with benign familial neonatal convulsions (BFNC)". Neurogenetics. 6 (4): 185–93. doi:10.1007/s10048-005-0012-2. hdl:2434/15127. PMID 16235065

Peripheral myelin protein 22 (1,472 words) [view diff] exact match in snippet view article find links to article

(March 2002). "Molecular cell biology of Charcot-Marie-Tooth disease". Neurogenetics. 4 (1): 1–15. doi:10.1007/s10048-002-0130-z. PMID 12030326. S2CID 25129077

Alexander Borst (640 words) [view diff] exact match in snippet view article find links to article

in olfactory learning in flies (Heisenberg, Borst, Wagner, Byers, J. Neurogenetics 1985). Since then, his work has focused on the question of how nerve

Octopamine (3,892 words) [view diff] exact match in snippet view article find links to article

synapses and contraction in Drosophila 3rd instar larvae". Journal of Neurogenetics. 32 (3): 183–194. doi:10.1080/01677063.2018.1502761. PMID 30303434.

Erich Jarvis (1,172 words) [view diff] exact match in snippet view article find links to article

Rockefeller University, where he is professor and head of the Laboratory of Neurogenetics of Language. The focus of Jarvis' research is the vocal learning capabilities

Mossy fiber (hippocampus) (1,671 words) [view diff] exact match in snippet view article

quantitative-genetic analysis of hippocampal variation in the mouse". Journal of Neurogenetics. 21 (4): 197–208. doi:10.1080/01677060701715827. PMID 18161583. S2CID 7334116

Huda Zoghbi (3,617 words) [view diff] exact match in snippet view article find links to article

2018. Jennings, Charles (4 March 2014). "McGovern Institute to honor neurogenetics researcher Huda Zoghbi". McGovern Institute for Brain Research. Archived

RTN1 (1,052 words) [view diff] exact match in snippet view article find links to article

paraplegia interacts with Reticulon 1 an endoplasmic reticulum protein". Neurogenetics. 7 (2): 93–103. doi:10.1007/s10048-006-0034-4. PMID 16602018. S2CID 8509463

Large neutral amino acids transporter small subunit 1 (897 words) [view diff] exact match in snippet view article find links to article

"Examination of association of genes in the serotonin system to autism". Neurogenetics. 10 (3): 209–16. doi:10.1007/s10048-009-0171-7. PMC 2753863. PMID 19184136

Jozef Gécz (149 words) [view diff] exact match in snippet view article find links to article

Year for 2019. Associate Professor Jozef Gécz, PhD, Laboratory Head, Neurogenetics Research Program Archived 8 April 2011 at the Wayback Machine Scientists

Germline mosaicism (1,432 words) [view diff] exact match in snippet view article find links to article

liquid chromatography in a EURO-MRX family with SLC6A8 deficiency". Neurogenetics. 9 (3): 183–190. doi:10.1007/s10048-008-0125-5. ISSN 1364-6753. PMID 18350323

National Institute of Neurological Disorders and Stroke (3,023 words) [view diff] exact match in snippet view article find links to article

Systems and Cognitive Neuroscience; Channels, Synapses, and Circuits; Neurogenetics; Neural Environment; and Neurodegeneration. Other working groups include:

Spinal and bulbar muscular atrophy (4,927 words) [view diff] exact match in snippet view article find links to article

Lieberman, Andrew P. (2018). "Spinal and bulbar muscular atrophy". Neurogenetics, Part II. Handbook of Clinical Neurology. Vol. 148. pp. 625–632. doi:10

Hesse (8,872 words) [view diff] exact match in snippet view article find links to article

Institute of Biophysics, Frankfurt-am-Main Max Planck Research Center for Neurogenetics [de], Frankfurt-am-Main Fraunhofer Institute for Translational Medicine

Jordan's syndrome (791 words) [view diff] exact match in snippet view article find links to article

with intellectual disability, macrocephaly, hypotonia, and autism". Neurogenetics. 17 (1): 43–49. doi:10.1007/s10048-015-0466-9. ISSN 1364-6753. PMC 4765493

Henry L. Paulson (458 words) [view diff] exact match in snippet view article find links to article

Yale University in 1990. He then completed a neurology residency and neurogenetics/movement disorders fellowship at the University of Pennsylvania. In

Dishabituation (1,467 words) [view diff] exact match in snippet view article find links to article

Sensitization but not Dishabituation in Drosophila Melanogaster". Journal of Neurogenetics. 21 (1): 59–71. doi:10.1080/01677060701249488. ISSN 0167-7063. PMC 2409174

Uncoordinated-119 (Unc-119) (1,611 words) [view diff] exact match in snippet view article

functionally conserved between humans, Drosophila and C. elegans". Journal of Neurogenetics. 13 (4): 191–212. doi:10.3109/01677060009084494. PMID 10858820. S2CID 36103225

Kenneth Blum (1,981 words) [view diff] exact match in snippet view article find links to article

Reward Deficiency Solution System (RDSS)™ as a function of dopaminergic neurogenetics and brain functional connectivity linking all addictions under a common

Computational neurogenetic modeling (2,259 words) [view diff] exact match in snippet view article find links to article

PMID 19003458. Kasabov, Nikola; Benuskova, Lubica (2004). "Computational Neurogenetics". Journal of Computational and Theoretical Nanoscience. 1: 47–61. CiteSeerX 10

LGI1 (1,532 words) [view diff] exact match in snippet view article find links to article

"LGI1: a gene involved in epileptogenesis and glioma progression?". Neurogenetics. 6 (2): 59–66. doi:10.1007/s10048-005-0216-5. PMID 15827762. S2CID 10999158

GBP2 (1,482 words) [view diff] exact match in snippet view article find links to article

for migraine without aura identified by exome sequencing". Journal of Neurogenetics. 29 (4): 188–194. doi:10.3109/01677063.2015.1122787. PMID 26814133.

Enhancer-FACS-seq (1,234 words) [view diff] exact match in snippet view article find links to article

PMID 14709165. Pfeiffer BD; et al. (2008). "Tools for neuroanatomy and neurogenetics in Drosophila". Proc Natl Acad Sci U S A. 105 (28): 9715–20. Bibcode:2008PNAS

Ashley Van Zeeland (1,193 words) [view diff] exact match in snippet view article find links to article

Function in Children with Autism Spectrum Disorders" using funding from a Neurogenetics Training Grant. After receiving her PhD, she worked as a consultant

Spastic paraplegia 6 (493 words) [view diff] exact match in snippet view article find links to article

with a pure form of autosomal dominant hereditary spastic paraplegia". Neurogenetics. 6 (2): 79–84. doi:10.1007/s10048-004-0209-9. ISSN 1364-6745. PMID 15711826

Dystrobrevin (2,558 words) [view diff] exact match in snippet view article find links to article

Kunkel LM (May 1997). "The genomic organization of human dystrobrevin". Neurogenetics. 1 (1): 37–42. doi:10.1007/s100480050006. PMID 10735273. S2CID 22588879

Optogenetics (11,915 words) [view diff] exact match in snippet view article find links to article

1016/S0092-8674(00)81826-7. PMID 8980237. S2CID 863399. Tsien JZ (2016). "Cre-Lox Neurogenetics: 20 Years of Versatile Applications in Brain Research and Counting…"

Cytochrome c oxidase subunit I (4,496 words) [view diff] exact match in snippet view article find links to article

denitrificans COX I gene explains functional deficits in a patient". Neurogenetics. 7 (1): 51–57. doi:10.1007/s10048-005-0015-z. PMID 16284789. S2CID 21304246

Rupert Glasgow (694 words) [view diff] exact match in snippet view article find links to article

University Press. R.D.V. Glasgow (2019). Minimal selfhood, Journal of Neurogenetics, DOI: 10.1080/01677063.2019.1672680 Translations (selection) Martha

Pathoclisis (1,269 words) [view diff] exact match in snippet view article find links to article

disease: mRNA profiles associated with higher brain tissue vulnerability. Neurogenetics 8, 83–94 (2007). https://doi.org/10.1007/s10048-006-0077-6 Xu, Jiang;

Serotonin (13,723 words) [view diff] exact match in snippet view article find links to article

for rewarded olfactory short-term memory in Drosophila". Journal of Neurogenetics. 26 (2): 238–244. doi:10.3109/01677063.2012.666298. PMID 22436011. S2CID 23639918

Norbert Perrimon (1,411 words) [view diff] exact match in snippet view article find links to article

Michele (2009-08-01). "A Drosophila resource of transgenic RNAi lines for neurogenetics". Genetics. 182 (4): 1089–1100. doi:10.1534/genetics.109.103630. ISSN 1943-2631

Drosophila connectome (2,317 words) [view diff] exact match in snippet view article find links to article

studies on Drosophila: a short perspective on a tiny brain". Journal of Neurogenetics. 30 (2): 62–68. doi:10.3109/01677063.2016.1166224. PMID 27328842. S2CID 21547224

MECP2 (3,589 words) [view diff] exact match in snippet view article find links to article

PMID 16708070. S2CID 28215286. Francke U (2007). "Mechanisms of disease: neurogenetics of MeCP2 deficiency". Nature Clinical Practice Neurology. 2 (4): 212–21

Goldberg–Shprintzen syndrome (1,327 words) [view diff] exact match in snippet view article find links to article

KIF1B-binding protein, in a familial case of fetal polymicrogyria". Neurogenetics. 14 (3–4): 215–224. doi:10.1007/s10048-013-0373-x. ISSN 1364-6753. PMID 24072599

Pavan Ramdya (1,308 words) [view diff] exact match in snippet view article find links to article

of Florian Engert. He then went on to perform postdoctoral work in neurogenetics and robotics in the laboratories of Richard Benton at University of

Michela Gallagher (2,039 words) [view diff] exact match in snippet view article find links to article

in 2008, holding the appointment for four years. She also leads the Neurogenetics and Behavior Center, located at Johns Hopkins University. Gallagher

Empathy (18,523 words) [view diff] exact match in snippet view article find links to article

tb00302.x. PMID 7965564. Todd RM, Anderson AK (November 2009). "The neurogenetics of remembering emotions past". Proceedings of the National Academy of

PLEKHG2 (1,151 words) [view diff] exact match in snippet view article find links to article

"Microcephaly-dystonia due to mutated PLEKHG2 with impaired actin polymerization". Neurogenetics. 17 (1): 25–30. doi:10.1007/s10048-015-0464-y. ISSN 1364-6753. PMID 26573021

Tim Tully (593 words) [view diff] exact match in snippet view article find links to article

was subsequently named Professor in 1995 and Head of the Division of Neurogenetics in 2006. In 1997, he and James Watson founded Helicon Therapeutics,

Charcot–Marie–Tooth disease (4,443 words) [view diff] exact match in snippet view article find links to article

(March 2002). "Molecular cell biology of Charcot-Marie-Tooth disease". Neurogenetics. 4 (1): 1–15. doi:10.1007/s10048-002-0130-z. PMID 12030326. S2CID 25129077

Hadassah Women's Zionist Organization of America (7,548 words) [view diff] exact match in snippet view article find links to article

Hadassah's department of Neurology, the Agnes Ginges Center for Human Neurogenetics. The research was funded in part by the National Institute of Neurological

Neuronal ceroid lipofuscinosis (4,409 words) [view diff] exact match in snippet view article find links to article

morphology and clinical phenotype in the neuronal ceroid lipofuscinoses". Neurogenetics. 6 (3): 107–26. doi:10.1007/s10048-005-0218-3. PMID 15965709. S2CID 9916771

Charlotte Sumner (658 words) [view diff] exact match in snippet view article find links to article

neuromuscular disease at Johns Hopkins School of Medicine. She was a fellow in neurogenetics in Kenneth Fischbeck's lab at the National Institute of Neurological

History of Tourette syndrome (4,917 words) [view diff] exact match in snippet view article find links to article

MW, Pittenger C (2018). "Tourette disorder and other tic disorders". Neurogenetics, Part I (Review). Handbook of Clinical Neurology. Vol. 147. pp. 343–54

Genetics of social behavior (2,165 words) [view diff] exact match in snippet view article find links to article

(904-908) Donaldson, Z.R. et al. (2008) "Oxytocin, Vasopressin, and the Neurogenetics of Sociality Archived 2016-09-10 at the Wayback Machine". Science 322

TTC19 (1,329 words) [view diff] exact match in snippet view article find links to article

with severe psychiatric manifestations and complex III deficiency". Neurogenetics. 14 (2): 153–60. doi:10.1007/s10048-013-0361-1. PMID 23532514. S2CID 6618051

Histone acetylation and deacetylation (7,036 words) [view diff] exact match in snippet view article find links to article

S2CID 14013417. Walker DM, Nestler EJ (2018). "Neuroepigenetics and addiction". Neurogenetics, Part II. Handbook of Clinical Neurology. Vol. 148. pp. 747–765. doi:10

Howard Lipshitz (1,461 words) [view diff] exact match in snippet view article find links to article

University with Douglas R. Kankel, working on Drosophila developmental neurogenetics. He then carried out postdoctoral research in the Biochemistry Department

George M. Martin (2,090 words) [view diff] exact match in snippet view article find links to article

CII allele with familial dementia of the Alzheimer type". Journal of Neurogenetics. 4 (2–3): 97–108. doi:10.3109/01677068709102337. PMID 2885403. Guo,

Mustafa Abdalla Mohamed Salih (979 words) [view diff] exact match in snippet view article find links to article

peer-reviewed articles and 30 book chapters on pediatric neurology, neurogenetics, neurodegenerative diseases and neuromuscular disorders. The articles

Management of Tourette syndrome (5,633 words) [view diff] exact match in snippet view article find links to article

MW, Pittenger C (2018). "Tourette disorder and other tic disorders". Neurogenetics, Part I (Review). Handbook of Clinical Neurology. Vol. 147. pp. 343–54

Edward Wild (neuroscientist) (2,433 words) [view diff] exact match in snippet view article

Journal of Huntington's Disease, the Association of British Neurologists Neurogenetics Advisory Panel, and the Translational Neurology Panel of the European

Cre-Lox recombination (5,058 words) [view diff] exact match in snippet view article find links to article

1073/pnas.92.26.12070. PMC 40298. PMID 8618846. Tsien JZ (2016). "Cre-Lox Neurogenetics: 20 Years of Versatile Applications in Brain Research and Counting…"

Reward system (13,122 words) [view diff] exact match in snippet view article find links to article

(help) Walker DM, Nestler EJ (2018). "Neuroepigenetics and addiction". Neurogenetics, Part II. Handbook of Clinical Neurology. Vol. 148. pp. 747–765. doi:10

ASPM (gene) (3,703 words) [view diff] exact match in snippet view article

microcephaly in 33 Pakistani families: Novel sequence variants in ASPM gene". Neurogenetics. 7 (2): 105–10. doi:10.1007/s10048-006-0042-4. PMID 16673149. S2CID 22685315

Ying-Hui Fu (2,257 words) [view diff] exact match in snippet view article find links to article

Retrieved 2018-10-14. "Science of Sleep - Biography". Science of Sleep. "Neurogenetics: Ying-Hui Fu". www.neugenes.org. Retrieved 2015-04-09. Schepens, Bert;

Ann B. Moser (383 words) [view diff] exact match in snippet view article find links to article

appointed as an associate professor of neurology in the department of neurogenetics at Johns Hopkins University. She is an associate professor emerita in

Ann B. Moser (383 words) [view diff] exact match in snippet view article find links to article

appointed as an associate professor of neurology in the department of neurogenetics at Johns Hopkins University. She is an associate professor emerita in

Yunis–Varon syndrome (2,976 words) [view diff] exact match in snippet view article find links to article

for bilateral occipital polymicrogyria maps to chromosome 6q16–q22". Neurogenetics. 10 (1): 35–42. doi:10.1007/s10048-008-0143-3. ISSN 1364-6745. PMID 18758830

Dan J. Stein (2,565 words) [view diff] exact match in snippet view article find links to article

research on anxiety, initiated brain magnetic resonance imaging and neurogenetics research in the country, and conducted the first nationally representative

Spinocerebellar ataxia type 1 (10,375 words) [view diff] exact match in snippet view article find links to article

Informed Choice About Genetic Testing" (PDF). University of Washington, Neurogenetics. National Institute on Disability and Rehabilitation Research. Retrieved

Andrew Kasarskis (1,733 words) [view diff] exact match in snippet view article find links to article

candidate causal sleep genes identified in an N2 cross". Journal of Neurogenetics. 25 (4): 167–81. doi:10.3109/01677063.2011.628426. PMC 3568991. PMID 22091728

Muscle–eye–brain disease (3,538 words) [view diff] exact match in snippet view article find links to article

muscle–eye–brain disease-like phenotype with multicystic leucodystrophy". Neurogenetics. 14 (3–4): 205–213. doi:10.1007/s10048-013-0374-9. ISSN 1364-6745. PMID 24052401

Pigment dispersing factor (3,793 words) [view diff] exact match in snippet view article find links to article

Studies in the Fly Brain to a Concept in Circadian Biology". Journal of Neurogenetics. 28 (3–4): 329–347. doi:10.3109/01677063.2014.905556. ISSN 0167-7063

Autosomal dominant leukodystrophy with autonomic disease (1,801 words) [view diff] exact match in snippet view article find links to article

autosomal dominant leukodystrophy (ADLD) with autonomic symptoms". Neurogenetics. 12 (1): 65–72. doi:10.1007/s10048-010-0269-y. ISSN 1364-6753. PMID 21225301

Major facilitator superfamily (5,029 words) [view diff] exact match in snippet view article find links to article

lipofuscinosis caused by MFSD8 mutations: a common theme emerging". Neurogenetics. 10 (4): 307–11. doi:10.1007/s10048-009-0185-1. PMID 19277732. S2CID 36438803

Science and technology in Morocco (5,359 words) [view diff] exact match in snippet view article find links to article

a third on condensed matter and systems modelling and a fourth on neurogenetics; The Moroccan Spin-off and Incubation Network (Réseau Maroc incubation

Conceição Bettencourt (484 words) [view diff] exact match in snippet view article find links to article

Bettencourt Alma mater University of the Azores Scientific career Fields Neurogenetics Neuroepigenetics Institutions UCL Queen Square Institute of Neurology

Matthew J. DeGennaro (1,775 words) [view diff] exact match in snippet view article find links to article

2008 and acquired a position in Leslie B. Vosshall's Laboratory of Neurogenetics and Behavior at The Rockefeller University. While working as a postdoctoral

Jeffrey Owen Katz (2,100 words) [view diff] exact match in snippet view article find links to article

36. Katz, Jeffrey Owen, and McCormick, Donna L. (July/August 1994). "Neurogenetics and Its Use in Trading System Development." NeuroVe$t Journal, pp. 8–11

Titles of distinction awarded by the University of Oxford (16,567 words) [view diff] exact match in snippet view article find links to article

Neff, Professor of Technology and Society Andrea Nemeth, Professor of Neurogenetics Jaideep Pandit, Professor of Anaesthesia Aris Theodosis Papageorghiou

2012 Australia Day Honours (133 words) [view diff] exact match in snippet view article find links to article

Nance North For service to medicine in the field of neuromuscular and neurogenetics research, paediatrics and child health as a clinician and academic,

Zoe R. Donaldson (1,611 words) [view diff] exact match in snippet view article find links to article

org. Retrieved May 28, 2020. Donaldson, Zoe R (2009). Exploring the neurogenetics of sociality: creation of models to assess the functional role of V1a

Facioscapulohumeral muscular dystrophy (16,335 words) [view diff] exact match in snippet view article find links to article

(FSHD) molecular diagnosis: from traditional technology to the NGS era". Neurogenetics. 20 (2): 57–64. doi:10.1007/s10048-019-00575-4. PMID 30911870. S2CID 85495566

Genetics of amyotrophic lateral sclerosis (3,945 words) [view diff] exact match in snippet view article find links to article

Dementia–Amyotrophic Lateral Sclerosis (FTD-ALS) Spectrum Disorders". Journal of Neurogenetics. 28 (1–2): 30–40. doi:10.3109/01677063.2013.876021. ISSN 0167-7063.

Biological tests of necessity and sufficiency (2,668 words) [view diff] exact match in snippet view article find links to article

logic in the field of biology, especially neuroscience". Journal of Neurogenetics. 32 (2): 53–64. doi:10.1080/01677063.2018.1468443. PMC 6510664. PMID 29757057

Familial sleep traits (3,472 words) [view diff] exact match in snippet view article find links to article

LJ, Fu YH (2018-01-01). "Disorders of sleep and circadian rhythms". Neurogenetics, Part II. Handbook of Clinical Neurology. Vol. 148. pp. 531–538. doi:10

Kristen Kroll (2,837 words) [view diff] exact match in snippet view article find links to article

Molecular, Cellular, and Developmental Neuroscience (MDCN) study section, Neurogenetics and Genomics Special Emphasis and Challenge Grants Panels, Neurogenesis

Endorsements in the 2016 United Kingdom European Union membership referendum (27,194 words) [view diff] exact match in snippet view article find links to article

The University of Manchester Professor Rita Horvath, Professor of Neurogenetics, Newcastle University Professor Rob Poole, Professor of Social Psychiatry

Carrie Bearden (1,663 words) [view diff] exact match in snippet view article find links to article

developmental psychopathology, brain imaging, biomarkers of psychosis risk and neurogenetics. Bearden has conducted research on copy number variants (CNVs) that

SMIM19 (2,273 words) [view diff] exact match in snippet view article find links to article

THAP1 deletion in familial basal ganglia calcification with dystonia". Neurogenetics. 15 (1): 23–30. doi:10.1007/s10048-013-0378-5. PMC 3969760. PMID 24135862