W F Crowley - Concepedia

Author

W F Crowley

Also Known As

W Crowley, W F Crowley, W F. Crowley, W. Crowley, W. Crowley,, W. F. CROWLEY, W. F. Crowley, W. F. Crowley Jr, W.F. CROWLEY, W.F. CROWLEY Jr

Publications

6.6K

Citations

H-Index

116

Concepts

All Affiliations

Massachusetts General Hospital Harvard University Boston Children's Hospital

About

W F Crowley is an author at Massachusetts General Hospital specializing in medicine, endocrinology, and obstetrics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	29	39	4.1K
2	Public Health	21	26	3.2K
3	Natural Sciences	3	3	237
4	Health Sciences	1	1	29
5	Nursing	1	1	19

W F Crowley

Publications

6.3K

Citations

H-Index

Page 1

	Year	Citations
A Role for Kisspeptins in the Regulation of Gonadotropin Secretion in the Mouse Michelle L. Gottsch, Matthew J. Cunningham, J. T. Smith, Endocrinology Kisspeptin SignalingFsh SecretionReproductive BiologyNeuroendocrine MechanismHypothalamic Peptide	2004	1.1K
Neuroendocrine regulation of the corpus luteum in the human. Evidence for pulsatile progesterone secretion. Marco Filicori, James P. Butler, W F Crowley Journal of Clinical Investigation Pulsatile Progesterone SecretionCorpus LuteumFertilityNeuroendocrinologyGynecology	1984	547
THERAPEUTIC USE OF PITUITARY OESENSITIZATION WITH A LONG-ACTING LHRM AGONIST: A POTENTIAL NEW TREATMENT FOR IDIOPATHIC PRECOCIOUS PUBERTY* W F Crowley, F. COMITF, Wylie Vale, The Journal of Clinical Endocrinology & Metabolism	1981	274
Adrenal hypoplasia congenita with hypogonadotropic hypogonadism: evidence that DAX-1 mutations lead to combined hypothalmic and pituitary defects in gonadotropin production. Reema L. Habiby, Paul A. Boepple, Lila E. Nachtigall, Journal of Clinical Investigation Dax-1 MutationsGeneticsPituitary DefectGynecologyPituitary Responsiveness	1996	257
Characterizing Discrete Subsets of Polycystic Ovary Syndrome as Defined by the Rotterdam Criteria: The Impact of Weight on Phenotype and Metabolic Features Corrine K. Welt, Johannes Gudmundsson, G. Arason, The Journal of Clinical Endocrinology & Metabolism	2006	257
Prevalence, Phenotypic Spectrum, and Modes of Inheritance of Gonadotropin-Releasing Hormone Receptor Mutations in Idiopathic Hypogonadotropic Hypogonadism<sup>1</sup> Milena Beranova, Luciana Mattos Barros Oliveira, Grégoy Y. Bédécarrats, The Journal of Clinical Endocrinology & Metabolism	2001	217
<i>CHD7</i> mutations in patients initially diagnosed with Kallmann syndrome – the clinical overlap with CHARGE syndrome M.C.J. Jongmans, CMA Van Ravenswaaij‐Arts, Nelly Pitteloud, Clinical Genetics	2008	208
Neuroendocrine-gonadal axis in men: frequent sampling of LH, FSH, and testosterone Daniel Spratt, Louis O’Dea, David Schoenfeld, American Journal of Physiology-Endocrinology and Metabolism Male PhysiologyFertilityFsh SecretionGynecologyReproductive Biology	1988	197
The genetic and clinical heterogeneity of gonadotropin-releasing hormone deficiency in the human. Joanne Waldstreicher, Stephanie B. Seminara, J. Larry Jameson, The Journal of Clinical Endocrinology & Metabolism Gnrh DeficiencyFertilityGeneticsReproductive HealthGenetic Epidemiology	1996	164
Hypothalamic gonadotropin-releasing hormone secretion and follicle-stimulating hormone dynamics during the luteal-follicular transition. Janet E. Hall, David Schoenfeld, K A Martin, The Journal of Clinical Endocrinology & Metabolism	1992	143

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