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Michael H. Polymeropoulos
Observed names:
M H Polymeropoulos,
M. H. Polymeropoulos,
M.H. Polymeropoulos
Observed institutions:
National Institutes of Health,
National Human Genome Research Institute,
National Institute of Neurological Disorders and Stroke,
Novartis (United States),
National Cancer Institute,
Eunice Kennedy Shriver National Institute of Child Health and Human Development
show all 6
OpenAlex ID:
A5110094863
Alpha synuclein in neurodegenerative disorders: Murderer or accomplice?
1998
·
E. Mezey
, A. Dehejia
, et al.
·
Nature Medicine
·
184
Predisposition of Wolfram syndrome heterozygotes to psychiatric illness
1998
·
R G Swift
, M H Polymeropoulos
, et al.
·
Molecular Psychiatry
·
132
A nonsense mutation in the cathepsin K gene observed in a family with pycnodysostosis.
1996
·
M R Johnson
, M H Polymeropoulos
, et al.
·
Genome Research
·
131
PDF
Linkage of Niemann-Pick disease type C to human chromosome 18.
1993
·
E D Carstea
, M H Polymeropoulos
, et al.
·
Proceedings of the National Academy of Sciences
·
119
Cloning, Chromosomal Localization, and Tissue Expression of Autotaxin from Human Teratocarcinoma Cells
1996
·
Hoi Young Lee
, Jun Murata
, et al.
·
Biochemical and Biophysical Research Communications
·
107
The human CAS (cellular apoptosis susceptibility) gene mapping on chromosome 20q13 is amplified in BT474 breast cancer cells and part of aberrant chromosomes in breast and colon cancer cell lines.
1996
·
U Brinkmann
, M Gallo
, et al.
·
Genome Research
·
98
PDF
A sporadic case of male-limited precocious puberty has the same constitutively activating point mutation in luteinizing hormone/choriogonadotropin receptor gene as familial cases
1994
·
K Yano
, A Hidaka
, et al.
·
The Journal of Clinical Endocrinology & Metabolism
·
67
Mutation screening of the Wolfram syndrome gene in psychiatric patients
2000
·
R Torres
, E Leroy
, et al.
·
Molecular Psychiatry
·
41
Exclusion of the MSX1 homeobox gene as the gene for the Ellis van Creveld syndrome in the Amish
1996
·
Susan E. Ide
, Rosa Isela Ortiz De Luna
, et al.
·
Human Genetics
·
12
The G209a Mutation In The α-synuclein Gene In Brazilian Families With Parkinson's Disease
2001
·
Teive H.A.G.
, Salmo Raskin
, et al.
·
Americanae (AECID Library)
Signing on to expression profiles
1999
·
Marlene M. Dressman
, Eric Holland
, et al.
·
Nature Genetics
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Works count:
11
Citation count:
891
H-index:
9
I10-index:
9
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