Literature DB >> 21076436

Copy number variation associated with Kallmann syndrome: new genetics insights from genome-wide studies.

Ericka B Trarbach.   

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Year:  2010        PMID： 21076436      PMCID： PMC3739183          DOI： 10.1038/aja.2010.115

Source DB:  PubMed          Journal:  Asian J Androl        ISSN： 1008-682X            Impact factor:   3.285


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  8 in total

Review 1.  Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability.

Authors:  Jacques S Beckmann; Xavier Estivill; Stylianos E Antonarakis
Journal:  Nat Rev Genet       Date:  2007-08       Impact factor: 53.242

2.  Clinical assessment and genomic landscape of a consanguineous family with three Kallmann syndrome descendants.

Authors:  Shi-Lin Zhang; Yan-Ping Tang; Tao Wang; Jun Yang; Ke Rao; Ling-Yun Zhao; Wen-Zhen Zhu; Xiang-Hu Meng; Shao-Gang Wang; Ji-Hong Liu; Wei-Min Yang; Zhang-Qun Ye
Journal:  Asian J Androl       Date:  2010-11-01       Impact factor: 3.285

Review 3.  Mechanisms of disease: Insights into X-linked and autosomal-dominant Kallmann syndrome.

Authors:  Pei-San Tsai; John C Gill
Journal:  Nat Clin Pract Endocrinol Metab       Date:  2006-03

Review 4.  The clinical context of copy number variation in the human genome.

Authors:  Charles Lee; Stephen W Scherer
Journal:  Expert Rev Mol Med       Date:  2010-03-09       Impact factor: 5.600

Review 5.  Genetics basis for GnRH-dependent pubertal disorders in humans.

Authors:  Leticia Ferreira Gontijo Silveira; Ericka Barbosa Trarbach; Ana Claudia Latronico
Journal:  Mol Cell Endocrinol       Date:  2010-02-25       Impact factor: 4.102

Review 6.  The complex genetics of Kallmann syndrome: KAL1, FGFR1, FGF8, PROKR2, PROK2, et al.

Authors:  J-P Hardelin; C Dodé
Journal:  Sex Dev       Date:  2008-11-05       Impact factor: 1.824

Review 7.  Hypogonadotropic hypogonadism.

Authors:  Lawrence C Layman
Journal:  Endocrinol Metab Clin North Am       Date:  2007-06       Impact factor: 4.741

8.  Systematic assessment of copy number variant detection via genome-wide SNP genotyping.

Authors:  Gregory M Cooper; Troy Zerr; Jeffrey M Kidd; Evan E Eichler; Deborah A Nickerson
Journal:  Nat Genet       Date:  2008-09-07       Impact factor: 38.330
  8 in total
  2 in total

1.  Recurrent deletions of the X chromosome linked CNV64, CNV67, and CNV69 shows geographic differences across China and no association with idiopathic infertility in men.

Authors:  Xiulan Ma; Martin Kuete; Xiuli Gu; Hui Zhou; Chengliang Xiong; Honggang Li
Journal:  PLoS One       Date:  2017-09-21       Impact factor: 3.240

Review 2.  A comprehensive review of genetics and genetic testing in azoospermia.

Authors:  Alaa J Hamada; Sandro C Esteves; Ashok Agarwal
Journal:  Clinics (Sao Paulo)       Date:  2013       Impact factor: 2.365
  2 in total

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