James S. Acierno - Concepedia

Author

James S. Acierno

Also Known As

Acierno J, Acierno, J.S., Acierno, James S, Acierno, James S., J S Acierno, J. Acierno, J. S. Acierno, JAMES S. ACIERNO, James S. Acierno, James Acierno

Publications

6.3K

Citations

H-Index

Concepts

All Affiliations

Massachusetts General Hospital University of Lausanne Harvard University Inserm New York University

About

James S. Acierno is an author at Massachusetts General Hospital specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	20	2K
2	Public Health	5	5	465
3	Social Sciences	3	3	321
4	Health Sciences	1	1	53
5	Biochemistry	1	1	53

James S. Acierno

Publications

5.9K

Citations

H-Index

Page 1

	Year	Citations
The <i>GPR54</i> Gene as a Regulator of Puberty Stephanie B. Seminara, Sophie Messager, Emmanouella E. Chatzidaki, New England Journal of Medicine	2003	2.5K
Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism Nelly Pitteloud, Richard Quinton, Simon H. S. Pearce, Journal of Clinical Investigation Gnrh DeficiencyIhh FamiliesDevelopmental BiologyMendelian DisorderGenetic Disorder	2007	376
The GPR54 Gene as a Regulator of Puberty Stephanie B. Seminara, Sophie Messager, Emmanouella E. Chatzidaki, Obstetrical & Gynecological Survey	2004	274
Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism Nelly Pitteloud, James S. Acierno, Astrid U. Meysing, Proceedings of the National Academy of Sciences Human GrowthGeneticsGynecologyPathologyKallmann Syndrome	2006	246
Vitamin d inhibition of prostate adenocarcinoma growth and metastasis in the dunning rat prostate model system Robert H. Getzenberg, Benjamin W. Light, Paul E. Lapco, Urology UrologyProstate Adenocarcinoma GrowthMedicineDunning RatBenign Prostatic Hyperplasia	1997	221
Biotin-Responsive Basal Ganglia Disease Maps to 2q36.3 and Is Due to Mutations in SLC19A3 Wenqi Zeng, Eiman A. Al-Yamani, James S. Acierno, The American Journal of Human Genetics Neurodegenerative DiseasesMolecular NeuroscienceMedicineDegenerative DiseaseNeuroscience	2005	215
Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes Nelly Pitteloud, Astrid U. Meysing, Richard Quinton, Molecular and Cellular Endocrinology FibrosisDevelopmental BiologyMendelian DisorderCell DivisionReproductive Phenotypes	2006	197
Reversible Kallmann Syndrome, Delayed Puberty, and Isolated Anosmia Occurring in a Single Family with a Mutation in the Fibroblast Growth Factor Receptor 1 Gene Nelly Pitteloud, James S. Acierno, Astrid U. Meysing, The Journal of Clinical Endocrinology & Metabolism	2005	160
Familial schwannomatosis Mia MacCollin, Camryn M. Willett, Bianca Heinrich, Neurology	2003	140
Characterization of the human nasal embryonic LHRH factor gene, NELF, and a mutation screening among 65 patients with idiopathic hypogonadotropic hypogonadism (IHH) Kiyonori Miura, James S. Acierno, Stephanie B. Seminara Journal of Human Genetics Developmental BiologyHuman GrowthGenetic DisorderGeneticsGenetic Epidemiology	2004	139

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