Rachel Wevrick - Concepedia

Author

Rachel Wevrick

University of Alberta ORCID

Also Known As

R Wevrick, R. Wevrick, Rachel Wevrick, Rachel Wevrick (288102), Wevrick, R., Wevrick, Rachel

Publications

4.9K

Citations

H-Index

142

Concepts

All Affiliations

University of Alberta University of Toronto Stanford University Howard Hughes Medical Institute Hospital for Sick Children

About

Rachel Wevrick is an author at University of Alberta specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	23	35	2.4K
2	Health Sciences	8	8	695
3	Natural Sciences	5	5	342
4	Engineering	3	3	62
5	Education	2	2	29

Rachel Wevrick

Publications

4.5K

Citations

H-Index

Page 1

	Year	Citations
A mouse model for Prader-Willi syndrome imprinting-centre mutations Tao Yang, Todd E. Adamson, James L. Resnick, Nature Genetics Knockout MouseDevelopmental BiologyGenetic DisorderGeneticsMolecular Genetics	1998	301
Regulation of autism-relevant behaviors by cerebellar–prefrontal cortical circuits Elyza Kelly, Fantao Meng, Hirofumi Fujita, Nature Neuroscience Neurodevelopmental DisordersAutism-relevant BehaviorsCognitive ScienceDevelopmental Cognitive NeuroscienceSyndromic Autism	2020	267
Identification of a novel paternally expressed gene in the Prader - Willi syndrome region Rachel Wevrick, Julie A. Kerns, Uta Francke Human Molecular Genetics	1994	244
The Necdin Gene is Deleted in Prader-Willi Syndrome and is Imprinted in Human and Mouse H. Robson MacDonald, Rachel Wevrick Human Molecular Genetics	1997	229
Long-range organization of tandem arrays of alpha satellite DNA at the centromeres of human chromosomes: high-frequency array-length polymorphism and meiotic stability. Rachel Wevrick, H.F. Willard Proceedings of the National Academy of Sciences DnaHigh-frequency Array-length PolymorphismCytogeneticsGeneticsMolecular Biology	1989	228
The imprinted gene Magel2 regulates normal circadian output James W. Bogenpohl, Maureen P. Howell, Rachel Wevrick, Nature Genetics Imprinted Gene Magel2Transcriptional RegulationMedicineGeneticsCryptochrome	2007	218
Disruption of the mouse necdin gene results in early post-natal lethality Matthieu Gérard, Lídia Hernandez, Rachel Wevrick, Nature Genetics Knockout MouseDevelopmental BiologyGeneticsPathogenesisApoptosis	1999	207
Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome Jocelyn M. Bischof, Colin L. Stewart, Rachel Wevrick Human Molecular Genetics Pws Neonatal FailureMetabolic DisorderGeneticsMolecular GeneticsDisease Gene Identification	2007	195
Essential role for the Prader–Willi syndrome protein necdin in axonal outgrowth Syann Lee, Christine L. Walker, Barbara Karten, Human Molecular Genetics	2005	133
Hyperphagia: Current concepts and future directions proceedings of the 2nd international conference on hyperphagia Steven B. Heymsfield, Nicole M. Avena, Leslie J. Baier, Obesity	2014	127

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