Genetic studies of human diversity in East Asia

Feng Zhang , Bing Su , Ya-ping Zhang , Li Jin
Philosophical Transactions of the Royal Society B 362 ( 1482) 987 -996

58
2007
Association of a TDRD1 variant with spermatogenic failure susceptibility in the Han Chinese

Xiao-Bin Zhu , Jian-Qi Lu , Er-Lei Zhi , Yong Zhu
Journal of Assisted Reproduction and Genetics 33 ( 8) 1099 -1104

5
2016
Genetic evidence supports demic diffusion of Han culture

Bo Wen , Hui Li , Daru Lu , Xiufeng Song
Nature 431 ( 7006) 302 -305

491
2004
Potocki-Lupski Syndrome: A Microduplication Syndrome Associated with Oropharyngeal Dysphagia and Failure to Thrive

Claudia Soler-Alfonso , Kathleen J. Motil , Catherine L. Turk , Patricia Robbins-Furman
The Journal of Pediatrics 158 ( 4) 655 -659

30
2011
Autism and other Neuropsychiatric Symptoms are Prevalent in Individuals with MECP2 Duplication Syndrome

Melissa B. Ramocki , Sarika U. Peters , Y. Jane Tavyev , Feng Zhang
Annals of Neurology 66 ( 6) 771 -782

309
2009
A TBX5 3'UTR variant increases the risk of congenital heart disease in the Han Chinese population.

Feng Wang , Dong Liu , Ran-Ran Zhang , Li-Wei Yu
Cell discovery 3 ( 1) 17026 -17026

28
2017
Assessing structural variation in a personal genome-towards a human reference diploid genome.

Adam C English , William J Salerno , Oliver A Hampton , Claudia Gonzaga-Jauregui
BMC Genomics 16 ( 1) 286 -286

123
2015
GJB1/Connexin 32 whole gene deletions in patients with X-linked Charcot–Marie–Tooth disease

Claudia Gonzaga-Jauregui , Feng Zhang , Charles F. Towne , Sat Dev Batish
Neurogenetics 11 ( 4) 465 -470

25
2010
A spatial analysis of genetic structure of human populations in China reveals distinct difference between maternal and paternal lineages.

Fuzhong Xue , Yi Wang , Shuhua Xu , Feng Zhang
European Journal of Human Genetics 16 ( 6) 705 -717

41
2008
Copy number variants of ABCF1, IL17REL, and FCGR3A are associated with the risk of gout

Zheng Dong , Yuan Li , Jingru Zhou , Shuai Jiang
Protein & Cell 8 ( 6) 467 -470

9
2017
Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements

Pengfei Liu , Ayelet Erez , Sandesh C Sreenath Nagamani , Shweta U Dhar
Cell 146 ( 6) 889 -903

321
2011
Biallelic Mutations in CFAP43 and CFAP44 Cause Male Infertility with Multiple Morphological Abnormalities of the Sperm Flagella

Shuyan Tang , Xiong Wang , Weiyu Li , Xiaoyu Yang
American Journal of Human Genetics 100 ( 6) 854 -864

218
2017
Association of polymorphisms in four bilirubin metabolism genes with serum bilirubin in three Asian populations.

Rong Lin , Xiaofeng Wang , Yi Wang , Feng Zhang
Human Mutation 30 ( 4) 609 -615

27
2009
The clinical spectrum associated with a chromosome 17 short arm proximal duplication (dup 17p11.2) in three patients.

Martine Doco-Fenzy , Muriel Holder-Espinasse , Eric Bieth , Corinne Magdelaine
American Journal of Medical Genetics Part A 146 ( 7) 917 -924

11
2008
Complex human chromosomal and genomic rearrangements

Feng Zhang , Claudia M.B. Carvalho , James R. Lupski
Trends in Genetics 25 ( 7) 298 -307

207
2009
Interaction between Y chromosome haplogroup O3* and 4-n-octylphenol exposure reduces the susceptibility to spermatogenic impairment in Han Chinese.

Weiyue Hu , Minjian Chen , Juan Ji , Yufeng Qin
Ecotoxicology and Environmental Safety 144 450 -455

1
2017
9
2013
Structural variation of the human genome: mechanisms, assays, and role in male infertility.

Claudia M.B. Carvalho , Feng Zhang , James R. Lupski
Systems Biology in Reproductive Medicine 57 3 -16

31
2011
12
2013
Mechanisms for human genomic rearrangements

Wenli Gu , Feng Zhang , James R Lupski
Pathogenetics 1 ( 1) 4 -4

716
2008