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Rachel Wevrick

Observed names: R Wevrick, R. Wevrick, Wevrick R, Wevrick, R, Wevrick, R., Wevrick, Rachel
Observed institutions: Howard Hughes Medical Institute, University of Alberta, University of Toronto, Hospital for Sick Children, Stanford Medicine, Neuroscience and Mental Health Institute, University of California, Davis, Stanford University
ORCID: 0000-0002-3343-5794
Observed ORCID: 0000-0002-3343-5794
OpenAlex ID: A5035254171
A mouse model for Prader-Willi syndrome imprinting-centre mutations
1998 · Tao Yang, Todd E. Adamson, et al. · Nature Genetics · 300
Regulation of autism-relevant behaviors by cerebellar–prefrontal cortical circuits
2020 · Elyza Kelly, Fantao Meng, et al. · Nature Neuroscience · 280
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Human centromeric DNAs
1997 · C. Lee, R. Wevrick, et al. · Human Genetics · 243
Identification of a novel paternally expressed gene in the Prader - Willi syndrome region
1994 · Rachel Wevrick, Julie A. Kerns, et al. · Human Molecular Genetics · 242
The imprinted gene Magel2 regulates normal circadian output
2007 · Serguei V Kozlov, James W Bogenpohl, et al. · Nature Genetics · 231
The Necdin Gene is Deleted in Prader-Willi Syndrome and is Imprinted in Human and Mouse
1997 · H. R. MacDonald, R. Wevrick · Human Molecular Genetics · 231
Long-range organization of tandem arrays of alpha satellite DNA at the centromeres of human chromosomes: high-frequency array-length polymorphism and meiotic stability.
1989 · R Wevrick, H F Willard · Proceedings of the National Academy of Sciences · 219
Disruption of the mouse necdin gene results in early post-natal lethality
1999 · Matthieu Gérard, Lidia Hernandez, et al. · Nature Genetics · 212
Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome
2007 · J. M. Bischof, C. L. Stewart, et al. · Human Molecular Genetics · 200
Essential role for the Prader–Willi syndrome protein necdin in axonal outgrowth
2005 · Syann Lee, Christine L. Walker, et al. · Human Molecular Genetics · 136
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Absence ofNdn, Encoding the Prader-Willi Syndrome-Deleted Genenecdin, Results in Congenital Deficiency of Central Respiratory Drive in Neonatal Mice
2003 · Jun Ren, Syann Lee, et al. · Journal of Neuroscience · 129
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Hyperphagia: Current concepts and future directions proceedings of the 2nd international conference on hyperphagia
2014 · Steven B. Heymsfield, Nicole M. Avena, et al. · Obesity · 128
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Necdin, a Prader-Willi syndrome candidate gene, regulates gonadotropin-releasing hormone neurons during development
2008 · N. L.G. Miller, R. Wevrick, et al. · Human Molecular Genetics · 106
An Imprinted Mouse Transcript Homologous to the Human Imprinted in Prader-Willi Syndrome (IPW) Gene
1997 · R. Wevrick, U. Francke · Human Molecular Genetics · 106
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Regionally reduced brain volume, altered serotonin neurochemistry, and abnormal behavior in mice null for the circadian rhythm output gene Magel2
2009 · Rebecca E. Mercer, Erin M. Kwolek, et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 103
Loss of Magel2, a Candidate Gene for Features of Prader-Willi Syndrome, Impairs Reproductive Function in Mice
2009 · Rebecca E. Mercer, Rachel Wevrick · PLoS ONE · 101
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Developmental Abnormalities of Neuronal Structure and Function in Prenatal Mice Lacking the Prader-Willi Syndrome Gene Necdin
2005 · Silvia Pagliardini, Jun Ren, et al. · American Journal Of Pathology · 99
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Magel2 Is Required for Leptin-Mediated Depolarization of POMC Neurons in the Hypothalamic Arcuate Nucleus in Mice
2013 · Rebecca E. Mercer, Sheldon D. Michaelson, et al. · PLoS Genetics · 84
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Impaired Hypothalamic Regulation of Endocrine Function and Delayed Counterregulatory Response to Hypoglycemia in Magel2-Null Mice
2011 · Alysa A. Tennese, Rachel Wevrick · Endocrinology · 84
Targeting the endocannabinoid/CB1 receptor system for treating obesity in Prader–Willi syndrome
2016 · Ibrahim Knani, Brian J. Earley, et al. · Molecular Metabolism · 75
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Physical map of the centromeric region of human chromosome 7: relationship between two distinct alpha satellite arrays
1991 · Rachel Wevrick, Huntington F. Willard · Nucleic Acids Research · 74
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Cloning and analysis of the murine Fanconi anemia group C cDNA
1993 · Rachel Wevrick, Carol A. Clarke, et al. · Human Molecular Genetics · 68
Necdin, a p53 target gene, regulates the quiescence and response to genotoxic stress of hematopoietic stem/progenitor cells
2012 · Takashi Asai, Yan Liu, et al. · Blood · 67
Structure of DNA near long tandem arrays of alpha satellite DNA at the centromere of human chromosome 7
1992 · Rachel Wevrick, Vicki P. Willard, et al. · Genomics · 64
The Prader-Willi syndrome proteins MAGEL2 and necdin regulate leptin receptor cell surface abundance through ubiquitination pathways
2017 · Tishani Methsala Wijesuriya, Leentje De Ceuninck, et al. · Human Molecular Genetics · 62
Works count: 104
Citation count: 4,871
H-index: 37
I10-index: 63
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