M H Polymeropoulos - Concepedia

Author

M H Polymeropoulos

National Institutes of Health

Also Known As

M H Polymeropoulos, M. H. Polymeropoulos, M.H. Polymeropoulos, Michael H. Polymeropoulos

Publications

904

Citations

H-Index

Concepts

All Affiliations

National Institutes of Health National Human Genome Research Institute National Cancer Institute

About

M H Polymeropoulos is an author at National Institutes of Health specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	716
2	Public Health	2	2	186
3	Cell Biology	2	2	209
4	Natural Sciences	1	1	131
5	Biology	1	1	12

M H Polymeropoulos

Publications

716

Citations

H-Index

Page 1

	Year	Citations
Predisposition of Wolfram syndrome heterozygotes to psychiatric illness Ronnie Gorman Swift, M H Polymeropoulos, Rosarelis Torres, Molecular Psychiatry Psychiatric DiseasePsychiatryGenetic DisorderGeneticsPsychiatric Genetics	1998	136
A nonsense mutation in the cathepsin K gene observed in a family with pycnodysostosis. M R Johnson, M H Polymeropoulos, Hans L. Vos, Genome Research SclerostinBone Morphogenic ProteinMedicineGeneticsPathogenesis	1996	131
Linkage of Niemann-Pick disease type C to human chromosome 18. Eugene D. Carstea, M H Polymeropoulos, Clarissa C. Parker, Proceedings of the National Academy of Sciences CytogeneticsGeneticsGenetic EpidemiologyHuman PolymorphismPathology	1993	120
Cloning, Chromosomal Localization, and Tissue Expression of Autotaxin from Human Teratocarcinoma Cells Hoi Young Lee, Jun Murata, Timothy Clair, Biochemical and Biophysical Research Communications Human CellChromosomal LocalizationOncogenic AgentMedicineTissue Expression	1996	106
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. Ulrich Brinkmann, Maria Gallo, M H Polymeropoulos, Genome Research PathologyCell DeathCancer BiologyTumor BiologyOncology	1996	103
A sporadic case of male-limited precocious puberty has the same constitutively activating point mutation in luteinizing hormone/choriogonadotropin receptor gene as familial cases. Koichi Yano, Akinari Hidaka, Motoyasu Saji, The Journal of Clinical Endocrinology & Metabolism GeneticsMolecular GeneticsReproductive BiologyPrecocious PubertyReproductive Endocrinology	1994	66
Mutation screening of the Wolfram syndrome gene in psychiatric patients Rosarelis Torres, Elizabeth C. LeRoy, Xun Hu, Molecular Psychiatry Mendelian DisorderPsychiatryGenetic DisorderGeneticsPsychiatric Genetics	2000	42
Exclusion of the MSX1 homeobox gene as the gene for the Ellis van Creveld syndrome in the Amish Susan Ide, Rosa Isela Ortiz De Luna, Clair A. Francomano, Human Genetics BiologyDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	1996	12

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