Literature DB >> 17959785

Rites of passage through puberty: a complex genetic ensemble.

J Larry Jameson1.   

Abstract

Mesh：

Year:  2007        PMID： 17959785      PMCID： PMC2077239          DOI： 10.1073/pnas.0708636104

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN： 0027-8424            Impact factor:   11.205


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  16 in total

Review 1.  Variation in the timing of puberty: clinical spectrum and genetic investigation.

Authors:  M R Palmert; P A Boepple
Journal:  J Clin Endocrinol Metab       Date:  2001-06       Impact factor: 5.958

Review 2.  Beyond Mendel: an evolving view of human genetic disease transmission.

Authors:  Jose L Badano; Nicholas Katsanis
Journal:  Nat Rev Genet       Date:  2002-10       Impact factor: 53.242

3.  Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism.

Authors:  Nelly Pitteloud; Richard Quinton; Simon Pearce; Taneli Raivio; James Acierno; Andrew Dwyer; Lacey Plummer; Virginia Hughes; Stephanie Seminara; Yu-Zhu Cheng; Wei-Ping Li; Gavin Maccoll; Anna V Eliseenkova; Shaun K Olsen; Omar A Ibrahimi; Frances J Hayes; Paul Boepple; Janet E Hall; Pierre Bouloux; Moosa Mohammadi; William Crowley
Journal:  J Clin Invest       Date:  2007-01-18       Impact factor: 14.808

4.  Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism.

Authors:  Nelly Pitteloud; Chengkang Zhang; Duarte Pignatelli; Jia-Da Li; Taneli Raivio; Lindsay W Cole; Lacey Plummer; Elka E Jacobson-Dickman; Pamela L Mellon; Qun-Yong Zhou; William F Crowley
Journal:  Proc Natl Acad Sci U S A       Date:  2007-10-24       Impact factor: 11.205

Review 5.  Neurobiological mechanisms of puberty in higher primates.

Authors:  Tony M Plant; Mandi L Barker-Gibb
Journal:  Hum Reprod Update       Date:  2004 Jan-Feb       Impact factor: 15.610

6.  The GPR54 gene as a regulator of puberty.

Authors:  Stephanie B Seminara; Sophie Messager; Emmanouella E Chatzidaki; Rosemary R Thresher; James S Acierno; Jenna K Shagoury; Yousef Bo-Abbas; Wendy Kuohung; Kristine M Schwinof; Alan G Hendrick; Dirk Zahn; John Dixon; Ursula B Kaiser; Susan A Slaugenhaupt; James F Gusella; Stephen O'Rahilly; Mark B L Carlton; William F Crowley; Samuel A J R Aparicio; William H Colledge
Journal:  N Engl J Med       Date:  2003-10-23       Impact factor: 91.245

7.  The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules.

Authors:  R Legouis; J P Hardelin; J Levilliers; J M Claverie; S Compain; V Wunderle; P Millasseau; D Le Paslier; D Cohen; D Caterina
Journal:  Cell       Date:  1991-10-18       Impact factor: 41.582

Review 8.  Genetic insights into human isolated gonadotropin deficiency.

Authors:  Ericka Barbosa Trarbach; Leticia Gontijo Silveira; Ana Claudia Latronico
Journal:  Pituitary       Date:  2007       Impact factor: 4.107

9.  Altered circadian and homeostatic sleep regulation in prokineticin 2-deficient mice.

Authors:  Wang-Ping Hu; Jia-Da Li; Chengkang Zhang; Lisa Boehmer; Jerome M Siegel; Qun-Yong Zhou
Journal:  Sleep       Date:  2007-03       Impact factor: 5.849

Review 10.  Molecular pathogenesis of Kallmann's syndrome.

Authors:  Steven Mark Cadman; Soo-Hyun Kim; Youli Hu; David González-Martínez; Pierre-Marc Bouloux
Journal:  Horm Res       Date:  2006-12-21
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  2 in total

Review 1.  Deciphering genetic disease in the genomic era: the model of GnRH deficiency.

Authors:  Gerasimos P Sykiotis; Nelly Pitteloud; Stephanie B Seminara; Ursula B Kaiser; William F Crowley
Journal:  Sci Transl Med       Date:  2010-05-19       Impact factor: 17.956

2.  Oligogenic basis of isolated gonadotropin-releasing hormone deficiency.

Authors:  Gerasimos P Sykiotis; Lacey Plummer; Virginia A Hughes; Margaret Au; Sadia Durrani; Sadhana Nayak-Young; Andrew A Dwyer; Richard Quinton; Janet E Hall; James F Gusella; Stephanie B Seminara; William F Crowley; Nelly Pitteloud
Journal:  Proc Natl Acad Sci U S A       Date:  2010-08-09       Impact factor: 11.205
  2 in total

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