MeiSunMD

Internal Medicine • Chelmsford, MA

Physician

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Office
2 Meeting House Rd
Chelmsford, MA 01824
Phone+1 978-256-5522

Fax+1 978-256-5399
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Education & Training

Mount Sinai Hospital Medical Center of ChicagoResidency, Internal Medicine, 2011 - 2014
Massachusetts General HospitalGenetics, 2003 - 2011
West China University of Medical SciencesClass of 1988

Certifications & Licensure

MA State Medical License 2014 - 2025
IL State Medical License 2011 - 2014
American Board of Internal Medicine Internal Medicine

Publications & Presentations

PubMed

23 citations
Rare Deleterious PARD3 Variants in the aPKC-Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction...
Xiaoli Chen, Yu An, Yonghui Gao, Liu Guo, Lei Rui, Hua Xie, Mei Sun, Siv Lam Hung, Xiaoming Sheng, Jizhen Zou, Yihua Bao, Hongyan Guan, Bo Niu, Zandong Li, Richard H. ...> ;Human Mutation. 2017 Apr 1
287 citations
KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant.
Christelle Golzio, Jason R. Willer, Michael E. Talkowski, Edwin C. Oh, Yu Taniguchi, Sébastien Jacquemont, Alexandre Reymond, Mei Sun, Akira Sawa, James F. Gusella, At...> ;Nature. 2012 May 17
58 citations
Copy number variation in familial Parkinson disease.
Nathan Pankratz, Alexandra Dumitriu, Kurt N. Hetrick, Mei Sun, Jeanne C. Latourelle, Jemma B. Wilk, Cheryl Halter, Kimberly F. Doheny, James F. Gusella, William C. Nic...> ;Plos One. 2011 Aug 2
41 citations
Prevalence of Incompletely Penetrant Huntington's Disease Alleles Among Individuals With Major Depressive Disorder
Roy H. Perlis, Jordan W. Smoller, Jayalakshmi S. Mysore, Mei Sun, Tammy Gillis, Shaun Purcell, Marcella Rietschel, Markus M. Nöthen, Stephanie H. Witt, Wolfgang Maier,...> ;The American Journal of Psychiatry. 2010 May 1
Genomewide association study for onset age in Parkinson disease.
Latourelle JC, Pankratz N, Dumitriu A, Wilk JB, Goldwurm S, Pezzoli G, Mariani CB, DeStefano AL, Halter C, Gusella JF, Nichols WC, Myers RH, Foroud T, PROGENI Investig...> ;BMC medical genetics. 2009-09-22
56 citations
BDNF, relative preference, and reward circuitry responses to emotional communication
Gregory P. Gasic, Jordan W. Smoller, Roy H. Perlis, Mei Sun, Sang Lee, Byoung Woo Kim, Myung Joo Lee, Daphne J. Holt, Anne J. Blood, Nikos Makris, D.K. Kennedy, Richar...> ;American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics. 2009 Sep 5
Genomewide association study for susceptibility genes contributing to familial Parkinson disease.
Pankratz N, Wilk JB, Latourelle JC, DeStefano AL, Halter C, Pugh EW, Doheny KF, Gusella JF, Nichols WC, Foroud T, Myers RH, PSG-PROGENI and GenePD Investigators, Coord...> ;Human genetics. 2008-11-06
79 citations
The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study
Jeanne C. Latourelle, Mei Sun, Mark F. Lew, Oksana Suchowersky, Christine Klein, Lawrence I. Golbe, Margery H. Mark, John H. Growdon, G. Frederick Wooten, Ray L. Watts...> ;BMC Medicine. 2008 Nov 5
27 citations
Herbicide exposure modifies GSTP1 haplotype association to Parkinson onset age: the GenePD Study.
Jemma B. Wilk, J. E. Tobin, Oksana Suchowersky, Holly A. Shill, Christine Klein, G. F. Wooten, Mark F. Lew, Margery H. Mark, Mark Guttman, Ray L. Watts, Carlos Singer,...> ;Neurology. 2006 Dec 26
107 citations
Lysosomal exocytosis is impaired in mucolipidosis type IV.
Janice M. LaPlante, Mei Sun, John L. Falardeau, Daisy Dai, Edward M. Brown, Susan A. Slaugenhaupt, Peter M. Vassilev> ;Molecular Genetics and Metabolism. 2006 Dec 1
114 citations
Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study.
Mei Sun, Jeanne C. Latourelle, G. Frederick Wooten, Mark F. Lew, Christine Klein, Holly A. Shill, Lawrence I. Golbe, Margery H. Mark, Brad A. Racette, Joel S. Perlmutt...> ;Archives of Neurology. 2006 Jun 1
126 citations
Identification and characterization of the single channel function of human mucolipin-1 implicated in mucolipidosis type IV, a disorder affecting the lysosomal pathway.
Janice M. LaPlante, John L. Falardeau, Mei Sun, Marie Kanazirska, Edward M. Brown, Susan A. Slaugenhaupt, Peter M. Vassilev> ;FEBS Letters. 2002 Dec 4
130 citations
The neurogenetics of mucolipidosis type IV
Gheona Altarescu, M. Sun, David F. Moore, J. A. Smith, Edythe Wiggs, B. I. Solomon, Nicholas J. Patronas, K. P. Frei, S. Gupta, Christine R. Kaneski, Oliver Quarrell, ...> ;Neurology. 2002 Aug 13
16 citations
Cloning and characterization of the mouse Mcoln1 gene reveals an alternatively spliced transcript not seen in humans
John L. Falardeau, John C. Kennedy, James S. Acierno, Mei Sun, Stefanie Stahl, Ehud Goldin, Susan A. Slaugenhaupt> ;BMC Genomics. 2002 Feb 5
10 citations
A physical and transcript map of the MCOLN1 gene region on human chromosome 19p13.3-p13.2.
James S. Acierno, John C. Kennedy, John L. Falardeau, Maire Leyne, Matthew C. Bromley, Matthew W. Colman, Mei Sun, Catherine Bove, Linda K. Ashworth, Lisa H. Chadwick,...> ;Genomics. 2001 Apr 15
327 citations
Mucolipidosis type IV is caused by mutations in a gene encoding a novel transient receptor potential channel
Mei Sun, Ehud Goldin, Stefanie Stahl, John L. Falardeau, John C. Kennedy, James S. Acierno, Catherine Bove, Christine R. Kaneski, James W. Nagle, Matthew C. Bromley, M...> ;Human Molecular Genetics. 2000 Oct 12
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