| Year |
Citation |
Score |
| 2023 |
Xiong J, Wang R, Chen G, Yang Y, Du P, Meng H, Ma M, Allen E, Tao L, Wang H, Jin L, Wang CC, Wen S. Inferring the demographic history of Hexi Corridor over the past two millennia from ancient genomes. Science Bulletin. PMID 38184385 DOI: 10.1016/j.scib.2023.12.031 |
0.526 |
|
| 2023 |
Tao L, Yuan H, Zhu K, Liu X, Guo J, Min R, He H, Cao D, Yang X, Zhou Z, Wang R, Zhao D, Ma H, Chen J, Zhao J, ... ... Jin L, et al. Ancient genomes reveal millet farming-related demic diffusion from the Yellow River into southwest China. Current Biology : Cb. PMID 37852263 DOI: 10.1016/j.cub.2023.09.055 |
0.57 |
|
| 2023 |
Li Y, Xiong Z, Zhang M, Hysi PG, Qian Y, Adhikari K, Weng J, Wu S, Du S, Gonzalez-Jose R, Schuler-Faccini L, Bortolini MC, Acuna-Alonzo V, Canizales-Quinteros S, Gallo C, ... Jin L, et al. Combined genome-wide association study of 136 quantitative ear morphology traits in multiple populations reveal 8 novel loci. Plos Genetics. 19: e1010786. PMID 37459304 DOI: 10.1371/journal.pgen.1010786 |
0.316 |
|
| 2023 |
Li Q, Zhao L, Zeng Y, Kuang Y, Guan Y, Chen B, Xu S, Tang B, Wu L, Mao X, Sun X, Shi J, Xu P, Diao F, Xue S, ... ... Jin L, et al. Large-scale analysis of de novo mutations identifies risk genes for female infertility characterized by oocyte and early embryo defects. Genome Biology. 24: 68. PMID 37024973 DOI: 10.1186/s13059-023-02894-0 |
0.306 |
|
| 2023 |
Liu C, Si W, Tu C, Tian S, He X, Wang S, Yang X, Yao C, Li C, Kherraf ZE, Ye M, Zhou Z, Ma Y, Gao Y, Li Y, ... ... Jin L, et al. Deficiency of primate-specific SSX1 induced asthenoteratozoospermia in infertile men and cynomolgus monkey and tree shrew models. American Journal of Human Genetics. PMID 36796361 DOI: 10.1016/j.ajhg.2023.01.016 |
0.76 |
|
| 2023 |
Ke H, Tang S, Guo T, Hou D, Jiao X, Li S, Luo W, Xu B, Zhao S, Li G, Zhang X, Xu S, Wang L, Wu Y, Wang J, ... Jin L, et al. Landscape of pathogenic mutations in premature ovarian insufficiency. Nature Medicine. PMID 36732629 DOI: 10.1038/s41591-022-02194-3 |
0.386 |
|
| 2023 |
Tian S, Wang Z, Liu L, Zhou Y, Lv Y, Tang D, Wang J, Jiang J, Wu H, Tang S, Wang G, Geng H, Tao F, Liu H, He X, ... ... Jin L, et al. A homozygous frameshift mutation in ADAD2 cause male infertility with spermatogenic impairments. Journal of Genetics and Genomics = Yi Chuan Xue Bao. PMID 36608931 DOI: 10.1016/j.jgg.2022.12.004 |
0.757 |
|
| 2023 |
Tian S, Tu C, He X, Meng L, Wang J, Tang S, Gao Y, Liu C, Wu H, Zhou Y, Lv M, Lin G, Jin L, Cao Y, Tang D, et al. Biallelic mutations in cause male infertility with severe MMAF and NOA. Journal of Medical Genetics. PMID 36593121 DOI: 10.1136/jmg-2022-108887 |
0.774 |
|
| 2022 |
Shang L, Ren S, Yang X, Zhang F, Jin L, Zhang X, Wu Y. EIF4ENIF1 variants in two patients with non-syndromic premature ovarian insufficiency. European Journal of Medical Genetics. 104597. PMID 36030004 DOI: 10.1016/j.ejmg.2022.104597 |
0.351 |
|
| 2022 |
Zhao L, Li Q, Kuang Y, Xu P, Sun X, Meng Q, Wang W, Zeng Y, Chen B, Fu J, Dong J, Zhu J, Luo Y, Gu H, Li C, ... ... Jin L, et al. Heterozygous loss-of-function variants in LHX8 cause female infertility characterized by oocyte maturation arrest. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 36029299 DOI: 10.1016/j.gim.2022.07.027 |
0.34 |
|
| 2022 |
Zhang X, Tang Z, Wang B, Zhou X, Zhou L, Zhang G, Tian J, Zhao Y, Yao Z, Tian L, Zhang S, Xia H, Jin L, Li C, Li S. Forensic Analysis and Genetic Structure Construction of Chinese Chongming Island Han Based on Y Chromosome STRs and SNPs. Genes. 13. PMID 36011274 DOI: 10.3390/genes13081363 |
0.339 |
|
| 2022 |
Liu C, Shen Y, Tang S, Wang J, Zhou Y, Tian S, Wu H, Cong J, He X, Jin L, Cao Y, Yang Y, Zhang F. Homozygous variants in induce asthenoteratozoospermia and male infertility. Journal of Medical Genetics. PMID 35228300 DOI: 10.1136/jmedgenet-2021-108271 |
0.783 |
|
| 2021 |
Wang Y, Chen Q, Zhang F, Yang X, Shang L, Ren S, Pan Y, Zhou Z, Li G, Fang Y, Jin L, Wu Y, Zhang X. Whole exome sequencing identified a rare WT1 loss-of-function variant in a non-syndromic POI patient. Molecular Genetics & Genomic Medicine. e1820. PMID 34845858 DOI: 10.1002/mgg3.1820 |
0.368 |
|
| 2021 |
Cong J, Wang X, Amiri-Yekta A, Wang L, Kherraf ZE, Liu C, Cazin C, Tang S, Hosseini SH, Tian S, Daneshipour A, Wang J, Zhou Y, Zeng Y, Yang S, ... ... Jin L, et al. Homozygous mutations in cause male infertility with oligoasthenoteratozoospermia in humans and mice. Journal of Medical Genetics. PMID 34348960 DOI: 10.1136/jmedgenet-2021-107919 |
0.774 |
|
| 2021 |
Liu C, Shen Y, Shen Q, Zhang W, Wang J, Tang S, Wu H, Tian S, Cong J, He X, Jin L, Zhang F, Jiang X, Cao Y. Novel Mutations in X-Linked, -Induced Asthenoteratozoospermia and Male Infertility. Cells. 10. PMID 34202084 DOI: 10.3390/cells10071594 |
0.793 |
|
| 2021 |
Li G, Yang X, Wang L, Pan Y, Chen S, Shang L, Zhang Y, Wu Y, Zhou Z, Chen Q, Zhang X, Zhang L, Wang Y, Li J, Jin L, et al. Haploinsufficiency in non-homologous end joining factor 1 induces ovarian dysfunction in humans and mice. Journal of Medical Genetics. PMID 33888552 DOI: 10.1136/jmedgenet-2020-107398 |
0.306 |
|
| 2021 |
Wang CC, Yeh HY, Popov AN, Zhang HQ, Matsumura H, Sirak K, Cheronet O, Kovalev A, Rohland N, Kim AM, Mallick S, Bernardos R, Tumen D, Zhao J, Liu YC, ... ... Jin L, et al. Genomic Insights into the Formation of Human Populations in East Asia. Nature. PMID 33618348 DOI: 10.1038/s41586-021-03336-2 |
0.596 |
|
| 2021 |
Liu C, Tu C, Wang L, Wu H, Houston BJ, Mastrorosa FK, Zhang W, Shen Y, Wang J, Tian S, Meng L, Cong J, Yang S, Jiang Y, Tang S, ... ... Jin L, et al. Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility. American Journal of Human Genetics. PMID 33472045 DOI: 10.1016/j.ajhg.2021.01.002 |
0.803 |
|
| 2020 |
Pan Y, Yang X, Zhang F, Chen S, Zhou Z, Yin H, Ma H, Shang L, Yang J, Li G, Wang Y, Jin L, Shi Q, Wu Y. A heterozygous hypomorphic mutation of Fanca causes impaired follicle development and subfertility in female mice. Molecular Genetics and Genomics : Mgg. PMID 33025164 DOI: 10.1007/s00438-020-01730-5 |
0.365 |
|
| 2020 |
Liu L, Liu W, Shi Y, Li L, Gao Y, Lei Y, Finnell R, Zhang T, Zhang F, Jin L, Li H, Tao W, Wang H. DVL mutations identified from human neural tube defects and Dandy-Walker malformation obstruct the Wnt signaling pathway. Journal of Genetics and Genomics = Yi Chuan Xue Bao. PMID 32900645 DOI: 10.1016/J.Jgg.2020.06.003 |
0.345 |
|
| 2020 |
Sun J, Wei LH, Wang LX, Huang YZ, Yan S, Cheng HZ, Ong RT, Saw WY, Fan ZQ, Deng XH, Lu Y, Zhang C, Xu SH, Jin L, Teo YY, et al. Paternal gene pool of Malays in Southeast Asia and its applications for the early expansion of Austronesians. American Journal of Human Biology : the Official Journal of the Human Biology Council. e23486. PMID 32851723 DOI: 10.1002/Ajhb.23486 |
0.376 |
|
| 2020 |
He X, Liu C, Yang X, Lv M, Ni X, Li Q, Cheng H, Liu W, Tian S, Wu H, Gao Y, Yang C, Tan Q, Cong J, Tang D, ... ... Jin L, et al. Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice. American Journal of Human Genetics. PMID 32791035 DOI: 10.1016/J.Ajhg.2020.07.010 |
0.794 |
|
| 2020 |
Chen Q, Ke H, Luo X, Wang L, Wu Y, Tang S, Li J, Jin L, Zhang F, Qin Y, Chen X. Rare deleterious BUB1B variants induce premature ovarian insufficiency and early menopause. Human Molecular Genetics. PMID 32716490 DOI: 10.1093/Hmg/Ddaa153 |
0.465 |
|
| 2020 |
Yin C, Su K, He Z, Zhai D, Guo K, Chen X, Jin L, Li S. Genetic Reconstruction and Forensic Analysis of Chinese Shandong and Yunnan Han Populations by Co-Analyzing Y Chromosomal STRs and SNPs. Genes. 11. PMID 32635262 DOI: 10.3390/Genes11070743 |
0.423 |
|
| 2020 |
Liu C, Miyata H, Gao Y, Sha Y, Tang S, Xu Z, Whitfield M, Patrat C, Wu H, Dulioust E, Tian S, Shimada K, Cong J, Noda T, Li H, ... Jin L, et al. Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility. American Journal of Human Genetics. PMID 32619401 DOI: 10.1016/J.Ajhg.2020.06.004 |
0.804 |
|
| 2020 |
Yang N, Wu N, Dong S, Zhang L, Zhao Y, Chen W, Du R, Song C, Ren X, Liu J, Pehlivan D, Liu Z, Jia R, Wang C, Zhao S, ... ... Jin L, et al. Human and mouse studies establish TBX6 in Mendelian CAKUT and as a potential driver of kidney defects associated with the 16p11.2 microdeletion syndrome. Kidney International. PMID 32450157 DOI: 10.1016/J.Kint.2020.04.045 |
0.557 |
|
| 2020 |
Ye J, Tong Y, Lv J, Peng R, Chen S, Kuang L, Su K, Zheng Y, Zhang T, Zhang F, Jin L, Yang X, Wang H. Rare mutations in the autophagy-regulating gene AMBRA1 contribute to human neural tube defects. Human Mutation. PMID 32333458 DOI: 10.1002/Humu.24028 |
0.43 |
|
| 2020 |
Wen SQ, Sun C, Song DL, Huang YZ, Tong XZ, Meng HL, Yao HB, Du PX, Wei LH, Wang LX, Wang CC, Shi MS, Lan YM, Wang JC, Jin L, et al. Y-chromosome evidence confirmed the Kerei-Abakh origin of Aksay Kazakhs. Journal of Human Genetics. PMID 32313196 DOI: 10.1038/S10038-020-0759-1 |
0.659 |
|
| 2020 |
Zhu Z, Jiang Y, Cui M, Wang Y, Li S, Xu K, Zhang K, Zhu C, Xu W, Jin L, Ye W, Suo C, Chen X. rs671 polymorphisms and the risk of cerebral microbleeds in Chinese elderly: the Taizhou Imaging Study. Annals of Translational Medicine. 8: 229. PMID 32309376 DOI: 10.21037/Atm.2020.01.01 |
0.328 |
|
| 2020 |
Yin C, Ren Y, Adnan A, Tian J, Guo K, Xia M, He Z, Zhai D, Chen X, Wang L, Li X, Qin X, Li S, Jin L. Title: Developmental validation of Y-SNP pedigree tagging system: A panel via quick ARMS PCR. Forensic Science International. Genetics. 46: 102271. PMID 32169809 DOI: 10.1016/J.Fsigen.2020.102271 |
0.308 |
|
| 2020 |
Lin R, Yuan Z, Zhang C, Ju H, Sun Y, Huang N, Chen L, Jin L. Common genetic variants in ADCY5 and gestational glycemic traits. Plos One. 15: e0230032. PMID 32163478 DOI: 10.1371/Journal.Pone.0230032 |
0.305 |
|
| 2020 |
Lv M, Liu W, Chi W, Ni X, Wang J, Cheng H, Li WY, Yang S, Wu H, Zhang J, Gao Y, Liu C, Li C, Yang C, Tan Q, ... ... Jin L, et al. Homozygous mutations in can induce asthenoteratospermia with severe MMAF. Journal of Medical Genetics. PMID 32051257 DOI: 10.1136/Jmedgenet-2019-106479 |
0.497 |
|
| 2019 |
Ren X, Yang N, Wu N, Xu X, Chen W, Zhang L, Li Y, Du RQ, Dong S, Zhao S, Chen S, Jiang LP, Wang L, Zhang J, Wu Z, ... Jin L, et al. Increased gene dosages induce congenital cervical vertebral malformations in humans and mice. Journal of Medical Genetics. PMID 31888956 DOI: 10.1136/Jmedgenet-2019-106333 |
0.553 |
|
| 2019 |
Xiong Z, Dankova G, Howe LJ, Lee MK, Hysi PG, de Jong MA, Zhu G, Adhikari K, Li D, Li Y, Pan B, Feingold E, Marazita ML, Shaffer JR, McAloney K, ... ... Jin L, et al. Novel genetic loci affecting facial shape variation in humans. Elife. 8. PMID 31763980 DOI: 10.7554/Elife.49898 |
0.355 |
|
| 2019 |
Liu C, He X, Liu W, Yang S, Wang L, Li W, Wu H, Tang S, Ni X, Wang J, Gao Y, Tian S, Zhang L, Cong J, Zhang Z, ... ... Jin L, et al. Bi-allelic Mutations in TTC29 Cause Male Subfertility with Asthenoteratospermia in Humans and Mice. American Journal of Human Genetics. PMID 31735294 DOI: 10.1016/J.Ajhg.2019.10.010 |
0.791 |
|
| 2019 |
Wang L, Zhang Y, Fu X, Dong S, Tang S, Zhang N, Song C, Yang N, Zhang L, Wang H, Shi H, Jin L, Zhang F, Li J, Hua K. Joint utilization of genetic analysis and semi-cloning technology reveals a digenic etiology of Müllerian anomalies. Cell Research. PMID 31628433 DOI: 10.1038/S41422-019-0243-7 |
0.375 |
|
| 2019 |
Yang X, Zhang X, Jiao J, Zhang F, Pan Y, Wang Q, Chen Q, Cai B, Tang S, Zhou Z, Chen S, Yin H, Fu W, Luo Y, Li D, ... ... Jin L, et al. Rare variants in FANCA induce premature ovarian insufficiency. Human Genetics. PMID 31535215 DOI: 10.1007/S00439-019-02059-9 |
0.499 |
|
| 2019 |
Liu Y, Gao W, Koellmann C, Le Clerc S, Hüls A, Li B, Peng Q, Wu S, Ding A, Yang Y, Jin L, Krutmann J, Schikowski T, Zagury JF, Wang S. Genome-wide scan identified genetic variants associated with skin aging in a Chinese female population. Journal of Dermatological Science. PMID 31522824 DOI: 10.1016/J.Jdermsci.2019.08.010 |
0.37 |
|
| 2019 |
Li W, Wu H, Li F, Tian S, Kherraf ZE, Zhang J, Ni X, Lv M, Liu C, Tan Q, Shen Y, Amiri-Yekta A, Cazin C, Zhang J, Liu W, ... ... Jin L, et al. Biallelic mutations in cause male infertility with multiple morphological abnormalities of the sperm flagella in humans and mice. Journal of Medical Genetics. PMID 31501240 DOI: 10.1136/Jmedgenet-2019-106344 |
0.79 |
|
| 2019 |
Qu R, Sang Q, Wang X, Xu Y, Chen B, Mu J, Zhang Z, Jin L, He L, Wang L. A homozygous mutation in CMAS causes autosomal recessive intellectual disability in a Kazakh family. Annals of Human Genetics. PMID 31495922 DOI: 10.1111/Ahg.12349 |
0.305 |
|
| 2019 |
Wang S, Xiang C, Mou L, Yang Y, Zhong R, Wang L, Sun C, Qin Z, Yang J, Qian J, Zhao Y, Wang Y, Pan X, Qie J, Jiang Y, ... ... Jin L, et al. Trans-acting nonsynonymous variant of FOXA1 predisposes to hepatocellular carcinoma through modulating FOXA1-ERα transcriptional program and may have undergone natural selection. Carcinogenesis. PMID 31400761 DOI: 10.1093/Carcin/Bgz136 |
0.346 |
|
| 2019 |
Wen SQ, Yao HB, Du PX, Wei LH, Tong XZ, Wang LX, Wang CC, Zhou BY, Shi MS, Zhabagin M, Wang J, Xu D, Jin L, Li H. Molecular genealogy of Tusi Lu's family reveals their paternal relationship with Jochi, Genghis Khan's eldest son. Journal of Human Genetics. PMID 31164702 DOI: 10.1038/S10038-019-0618-0 |
0.639 |
|
| 2019 |
Liu C, Lv M, He X, Zhu Y, Amiri-Yekta A, Li W, Wu H, Kherraf ZE, Liu W, Zhang J, Tan Q, Tang S, Zhu YJ, Zhong Y, Li C, ... ... Jin L, et al. Homozygous mutations in induce multiple morphological abnormalities of the sperm flagella and male infertility. Journal of Medical Genetics. PMID 31048344 DOI: 10.1136/Jmedgenet-2019-106011 |
0.798 |
|
| 2019 |
Wang Y, Li Y, Hao M, Liu X, Zhang M, Wang J, Xiong M, Shugart YY, Jin L. Robust Reference Powered Association Test of Genome-Wide Association Studies. Frontiers in Genetics. 10: 319. PMID 31024629 DOI: 10.3389/Fgene.2019.00319 |
0.31 |
|
| 2019 |
Liu W, He X, Yang S, Zouari R, Wang J, Wu H, Kherraf ZE, Liu C, Coutton C, Zhao R, Tang D, Tang S, Lv M, Fang Y, Li W, ... ... Jin L, et al. Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice. American Journal of Human Genetics. PMID 30929735 DOI: 10.1016/J.Ajhg.2019.02.020 |
0.519 |
|
| 2019 |
Wang CC, Lu Y, Kang L, Ding H, Yan S, Guo J, Zhang Q, Wen SQ, Wang LX, Zhang M, Tong X, Huang X, Nie S, Deng Q, Zhu B, ... Jin L, et al. The massive assimilation of indigenous East Asian populations in the origin of Muslim Hui people inferred from paternal Y chromosome. American Journal of Physical Anthropology. PMID 30889274 DOI: 10.1002/Ajpa.23823 |
0.613 |
|
| 2019 |
Mu J, Wang W, Chen B, Wu L, Li B, Mao X, Zhang Z, Fu J, Kuang Y, Sun X, Li Q, Jin L, He L, Sang Q, Wang L. Mutations in and cause female infertility characterised by early embryonic arrest. Journal of Medical Genetics. PMID 30877238 DOI: 10.1136/Jmedgenet-2018-105936 |
0.303 |
|
| 2019 |
Liu J, Wu N, Yang N, Takeda K, Chen W, Li W, Du R, Liu S, Zhou Y, Zhang L, Liu Z, Zuo Y, Zhao S, Blank R, ... ... Jin L, et al. TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 30636772 DOI: 10.1038/s41436-018-0377-x |
0.391 |
|
| 2019 |
Dong S, Wang C, Li X, Shen Q, Fu X, Wu M, Song C, Yang N, Wu Y, Wang H, Jin L, Xu H, Zhang F. Noncoding rare variants of TBX6 in congenital anomalies of the kidney and urinary tract. Molecular Genetics and Genomics : Mgg. PMID 30604070 DOI: 10.1007/S00438-018-1522-6 |
0.429 |
|
| 2019 |
Wang Q, Li D, Cai B, Chen Q, Li C, Wu Y, Jin L, Wang X, Zhang X, Zhang F. Whole-exome sequencing reveals SALL4 variants in premature ovarian insufficiency: an update on genotype-phenotype correlations. Human Genetics. PMID 30603774 DOI: 10.1007/S00439-018-1962-4 |
0.461 |
|
| 2019 |
Xiong Z, Dankova G, Howe LJ, Lee MK, Hysi PG, Jong MAd, Zhu G, Adhikari K, Li D, Li Y, Pan B, Feingold E, Marazita ML, Shaffer JR, McAloney K, ... ... Jin L, et al. Author response: Novel genetic loci affecting facial shape variation in humans Elife. DOI: 10.7554/Elife.49898.Sa2 |
0.315 |
|
| 2019 |
Zhang M, Zheng H, Yan S, Jin L. Reconciling the father tongue and mother tongue hypotheses in Indo-European populations National Science Review. 6: 293-300. DOI: 10.1093/Nsr/Nwy083 |
0.353 |
|
| 2018 |
Liu W, Wu H, Wang L, Yang X, Liu C, He X, Li W, Wang J, Chen Y, Wang H, Gao Y, Tang S, Yang S, Jin L, Zhang F, et al. Homozygous loss-of-function mutations in FSIP2 cause male infertility with asthenoteratospermia. Journal of Genetics and Genomics = Yi Chuan Xue Bao. PMID 30745215 DOI: 10.1016/J.Jgg.2018.09.006 |
0.424 |
|
| 2018 |
He X, Li W, Wu H, Lv M, Liu W, Liu C, Zhu F, Li C, Fang Y, Yang C, Cheng H, Zhang J, Tan J, Chen T, Tang D, ... ... Jin L, et al. Novel homozygous mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagella. Journal of Medical Genetics. PMID 30415212 DOI: 10.1136/Jmedgenet-2018-105486 |
0.513 |
|
| 2018 |
Liu Q, Ma A, Wei L, Pang Y, Wu B, Luo T, Zhou Y, Zheng HX, Jiang Q, Gan M, Zuo T, Liu M, Yang C, Jin L, Comas I, et al. China's tuberculosis epidemic stems from historical expansion of four strains of Mycobacterium tuberculosis. Nature Ecology & Evolution. PMID 30397300 DOI: 10.1038/S41559-018-0680-6 |
0.309 |
|
| 2018 |
Li W, He X, Yang S, Liu C, Wu H, Liu W, Lv M, Tang D, Tan J, Tang S, Chen Y, Wang J, Zhang Z, Wang H, Jin L, et al. Biallelic mutations of CFAP251 cause sperm flagellar defects and human male infertility. Journal of Human Genetics. PMID 30310178 DOI: 10.1038/S10038-018-0520-1 |
0.544 |
|
| 2018 |
Yang N, Wu N, Zhang L, Zhao Y, Liu J, Liang X, Ren X, Li W, Chen W, Dong S, Zhao S, Lin J, Xiang H, Xue H, Chen L, ... ... Jin L, et al. TBX6 compound inheritance leads to congenital vertebral malformations in humans and mice. Human Molecular Genetics. PMID 30307510 DOI: 10.1093/Hmg/Ddy358 |
0.571 |
|
| 2018 |
Chen B, Wang W, Peng X, Jiang H, Zhang S, Li D, Li B, Fu J, Kuang Y, Sun X, Wang X, Zhang Z, Wu L, Zhou Z, Lyu Q, ... ... Jin L, et al. The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility. European Journal of Human Genetics : Ejhg. PMID 30297906 DOI: 10.1038/S41431-018-0283-3 |
0.331 |
|
| 2018 |
Wu S, Zhang M, Yang X, Peng F, Zhang J, Tan J, Yang Y, Wang L, Hu Y, Peng Q, Li J, Liu Y, Guan Y, Chen C, Hamer MA, ... ... Jin L, et al. Genome-wide association studies and CRISPR/Cas9-mediated gene editing identify regulatory variants influencing eyebrow thickness in humans. Plos Genetics. 14: e1007640. PMID 30248107 DOI: 10.1371/Journal.Pgen.1007640 |
0.433 |
|
| 2018 |
Wang C, Pu W, Zhao D, Zhou Y, Lu T, Chen S, He Z, Feng X, Wang Y, Li C, Li S, Jin L, Guo S, Wang J, Wang M. Identification of Hyper-Methylated Tumor Suppressor Genes-Based Diagnostic Panel for Esophageal Squamous Cell Carcinoma (ESCC) in a Chinese Han Population. Frontiers in Genetics. 9: 356. PMID 30233644 DOI: 10.3389/Fgene.2018.00356 |
0.301 |
|
| 2018 |
Feng W, Guo X, Huang H, Xu C, Li Y, Guo S, Zhao Z, Li Q, Lu D, Jin L, Wang J, Jiang G, Wu J. Polymorphism rs3819102 in thymidylate synthase and environmental factors: effects on lung cancer in Chinese population. Current Problems in Cancer. PMID 30180988 DOI: 10.1016/J.Currproblcancer.2018.07.005 |
0.323 |
|
| 2018 |
Hu P, Jiao R, Jin L, Xiong M. Application of Causal Inference to Genomic Analysis: Advances in Methodology. Frontiers in Genetics. 9: 238. PMID 30042787 DOI: 10.3389/Fgene.2018.00238 |
0.317 |
|
| 2018 |
Wei LH, Wang LX, Wen SQ, Yan S, Canada R, Gurianov V, Huang YZ, Mallick S, Biondo A, O'Leary A, Wang CC, Lu Y, Zhang C, Jin L, Xu S, et al. Paternal origin of Paleo-Indians in Siberia: insights from Y-chromosome sequences. European Journal of Human Genetics : Ejhg. PMID 29991739 DOI: 10.1038/S41431-018-0211-6 |
0.647 |
|
| 2018 |
Wang LX, Lu Y, Zhang C, Wei LH, Yan S, Huang YZ, Wang CC, Mallick S, Wen SQ, Jin L, Xu SH, Li H. Reconstruction of Y-chromosome phylogeny reveals two neolithic expansions of Tibeto-Burman populations. Molecular Genetics and Genomics : Mgg. PMID 29923068 DOI: 10.1007/S00438-018-1461-2 |
0.661 |
|
| 2018 |
Sun C, Zhang Z, Qie J, Wang Y, Qian J, Wang J, Wu J, Li Q, Bai C, Han B, Gao Z, Xu J, Lu D, Jin L, Wang H. Genetic polymorphism of is associated with clinical outcomes of platinum-based chemotherapy in non-small-cell lung cancer patients through modulating microRNA-mediated regulation. Oncotarget. 9: 23860-23877. PMID 29844858 DOI: 10.18632/Oncotarget.24794 |
0.325 |
|
| 2018 |
Wang X, Song D, Mykytenko D, Kuang Y, Lv Q, Li B, Chen B, Mao X, Xu Y, Zukin V, Mazur P, Mu J, Yan Z, Zhou Z, Li Q, ... ... Jin L, et al. Novel mutations in genes encoding subcortical maternal complex proteins may cause human embryonic developmental arrest. Reproductive Biomedicine Online. PMID 29606347 DOI: 10.1016/J.Rbmo.2018.03.009 |
0.314 |
|
| 2018 |
Sang Q, Li B, Kuang Y, Wang X, Zhang Z, Chen B, Wu L, Lyu Q, Fu Y, Yan Z, Mao X, Xu Y, Mu J, Li Q, Jin L, et al. Homozygous Mutations in WEE2 Cause Fertilization Failure and Female Infertility. American Journal of Human Genetics. PMID 29606300 DOI: 10.1016/J.Ajhg.2018.02.015 |
0.321 |
|
| 2018 |
Dong Z, Zhou J, Xu X, Jiang S, Li Y, Zhao D, Yang C, Ma Y, Wang Y, He H, Ji H, Zhang J, Yuan Z, Yang Y, Wang X, ... ... Jin L, et al. Genetic variants in two pathways influence serum urate levels and gout risk: a systematic pathway analysis. Scientific Reports. 8: 3848. PMID 29497127 DOI: 10.1038/S41598-018-21858-0 |
0.327 |
|
| 2018 |
Gao P, Yang X, Suo C, Yuan Z, Cheng H, Zhang Y, Jin L, Lu M, Chen X, Ye W. Socioeconomic status is inversely associated with esophageal squamous cell carcinoma risk: results from a population-based case-control study in China. Oncotarget. 9: 6911-6923. PMID 29467939 DOI: 10.18632/Oncotarget.24003 |
0.302 |
|
| 2018 |
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Wang F, Liu D, Zhang RR, Yu LW, Zhao JY, Yang XY, Jiang SS, Ma D, Qiao B, Zhang F, Jin L, Gui YH, Wang HY. A TBX5 3'UTR variant increases the risk of congenital heart disease in the Han Chinese population. Cell Discovery. 3: 17026. PMID 28761722 DOI: 10.1038/Celldisc.2017.26 |
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Zhang C, Lu J, Lou H, Du R, Xu S, Shen Y, Zhang F, Jin L. CNVbase: Batch identification of novel and rare copy number variations based on multi-ethnic population data. Journal of Genetics and Genomics = Yi Chuan Xue Bao. PMID 28739046 DOI: 10.1016/J.Jgg.2017.07.001 |
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Hu W, Chen M, Ji J, Qin Y, Zhang F, Xu M, Wu W, Du G, Wu D, Han X, Jin L, Xia Y, Lu C, Wang X. Interaction between Y chromosome haplogroup O3(*) and 4-n-octylphenol exposure reduces the susceptibility to spermatogenic impairment in Han Chinese. Ecotoxicology and Environmental Safety. 144: 450-455. PMID 28667856 DOI: 10.1016/J.Ecoenv.2017.06.038 |
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Tang S, Wang X, Li W, Yang X, Li Z, Liu W, Li C, Zhu Z, Wang L, Wang J, Zhang L, Sun X, Zhi E, Wang H, Li H, ... Jin L, et al. Biallelic Mutations in CFAP43 and CFAP44 Cause Male Infertility with Multiple Morphological Abnormalities of the Sperm Flagella. American Journal of Human Genetics. PMID 28552195 DOI: 10.1016/J.Ajhg.2017.04.012 |
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Liu Z, Burgess S, Wang Z, Deng W, Chu X, Cai J, Zhu Y, Shi J, Xie X, Wang Y, Jin L, Wang X. Associations of triglyceride levels with longevity and frailty: A Mendelian randomization analysis. Scientific Reports. 7: 41579. PMID 28134330 DOI: 10.1038/Srep41579 |
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Liu X, Lu D, Saw WY, Shaw PJ, Wangkumhang P, Ngamphiw C, Fucharoen S, Lert-Itthiporn W, Chin-Inmanu K, Chau TN, Anders K, Kasturiratne A, de Silva HJ, Katsuya T, Kimura R, ... ... Jin L, et al. Characterising private and shared signatures of positive selection in 37 Asian populations. European Journal of Human Genetics : Ejhg. PMID 28098149 DOI: 10.1038/Ejhg.2016.181 |
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Gao W, Tan J, Hüls A, Ding A, Liu Y, Matsui MS, Vierkötter A, Krutmann J, Schikowski T, Jin L, Wang S. Genetic variants associated with skin aging in the Chinese Han population. Journal of Dermatological Science. PMID 28057405 DOI: 10.1016/J.Jdermsci.2016.12.017 |
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Seow WJ, Matsuo K, Hsiung CA, Shiraishi K, Song M, Kim HN, Wong MP, Hong YC, Dean Hosgood H, Wang Z, Chang IS, Wang JC, Chatterjee N, Tucker M, Wei H, ... ... Jin L, et al. Association between GWAS-identified lung adenocarcinoma susceptibility loci and EGFR mutations in never-smoking Asian women, and comparison with findings from Western populations. Human Molecular Genetics. PMID 28025329 DOI: 10.1093/Hmg/Ddw414 |
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Zhang M, Li B, Wu S, Tan J, Yang Y, Marini A, Vierkötter A, Zhang J, Li H, Schikowski T, Jin L, Krutmann J, Wang S. A genome-wide association study of basal transepidermal water loss finds variants at 9q34.3 to be associated with skin barrier function. The Journal of Investigative Dermatology. PMID 28011148 DOI: 10.1016/J.Jid.2016.11.030 |
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Wang M, Li Q, Gu C, Zhu Y, Yang Y, Wang J, Jin L, He J, Ye D, Wei Q. Polymorphisms in nucleotide excision repair genes and risk of primary prostate cancer in Chinese Han populations. Oncotarget. PMID 27974699 DOI: 10.18632/Oncotarget.13848 |
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Yao HB, Wang CC, Tao X, Shang L, Wen SQ, Zhu B, Kang L, Jin L, Li H. Genetic evidence for an East Asian origin of Chinese Muslim populations Dongxiang and Hui. Scientific Reports. 6: 38656. PMID 27924949 DOI: 10.1038/Srep38656 |
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Jia M, Zhu M, Zhou F, Wang M, Sun M, Yang Y, Wang X, Wang J, Jin L, Xiang J, Zhang Y, Chang J, Wei Q. Genetic variants of JNK and p38α pathways and risk of non-small cell lung cancer in an Eastern Chinese population. International Journal of Cancer. PMID 27861856 DOI: 10.1002/Ijc.30508 |
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Wei LH, Yan S, Yu G, Huang YZ, Yao DL, Li SL, Jin L, Li H. Genetic trail for the early migrations of Aisin Gioro, the imperial house of the Qing dynasty. Journal of Human Genetics. PMID 27853133 DOI: 10.1038/Jhg.2016.142 |
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Cheng L, Qiu LX, Jia M, Zhou F, Wang MY, Zhang RX, Yang Y, Wang X, Wang J, Jin L, Wei QY. Is there a dose-dependent effect of genetic susceptibility loci for gastric cancer on prognosis of the patients? Oncotarget. PMID 27821817 DOI: 10.18632/Oncotarget.13123 |
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Wang P, Rahman M, Jin L, Xiong M. A new statistical framework for genetic pleiotropic analysis of high dimensional phenotype data. Bmc Genomics. 17: 881. PMID 27821073 DOI: 10.1186/S12864-016-3169-1 |
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Chen X, Yuan Z, Lu M, Zhang Y, Jin L, Ye W. Poor oral health is associated with an increased risk of esophageal squamous cell carcinoma - a population-based case-control study in China. International Journal of Cancer. PMID 27778330 DOI: 10.1002/Ijc.30484 |
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Sun H, Xu S, Long F, Luo J, Lin X, Jin L, Li L, Li S. Forensic and population genetic analysis of Han, Miao, Tujia and Gelao populations from Zunyi (Southwest China) on 15 autosomal short tandem repeat loci. Forensic Science International. Genetics. PMID 27592375 DOI: 10.1016/J.Fsigen.2016.08.007 |
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Wang CC, Huang Y, Yu X, Chen C, Jin L, Li H. Agriculture driving male expansion in Neolithic Time. Science China. Life Sciences. PMID 27132019 DOI: 10.1007/S11427-016-5057-Y |
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Xia ZG, Yin HF, Long Y, Cheng L, Yu LJ, Guo WJ, Zhu XD, Li J, Wang YN, Yang YJ, Wang JC, Jin L, Qiu LX, Wei Y. Genetic variant of miR-146a rs2910164 C>G and gastric cancer susceptibility. Oncotarget. PMID 27105532 DOI: 10.18632/Oncotarget.8814 |
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Qu R, Sang Q, Xu Y, Feng R, Jin L, He L, Wang L. Identification of a novel homozygous mutation in MYO3A in a Chinese family with DFNB30 non-syndromic hearing impairment. International Journal of Pediatric Otorhinolaryngology. 84: 43-7. PMID 27063751 DOI: 10.1016/J.Ijporl.2016.02.036 |
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Zhou F, Cheng L, Qiu LX, Wang MY, Li J, Sun MH, Yang YJ, Wang JC, Jin L, Wang YN, Wei QY. Associations of potentially functional variants in IL-6, JAKs and STAT3 with gastric cancer risk in an eastern Chinese population. Oncotarget. PMID 27049718 DOI: 10.18632/Oncotarget.8492 |
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Guo S, Li Y, Wang Y, Chu H, Chen Y, Liu Q, Guo G, Tu W, Wu W, Zou H, Yang L, Xiao R, Ma Y, Zhang F, Xiong M, ... Jin L, et al. Copy Number Variation of HLA-DQA1 and APOBEC3A/3B Contribute to the Susceptibility of Systemic Sclerosis in the Chinese Han Population. The Journal of Rheumatology. PMID 27036383 DOI: 10.3899/Jrheum.150945 |
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Liu ZY, Wang ZD, Li LZ, Chu XF, Zhu YS, Shi JM, Xie XJ, Jin L, Wang Y, Wang XF. Association of CRP gene polymorphisms with CRP levels, frailty and co-morbidity in an elderly Chinese population: results from RuLAS. Age and Ageing. PMID 27016573 DOI: 10.1093/Ageing/Afw041 |
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Yang J, Yang Y, Xia M, Wang L, Zhou W, Yang Y, Jiang Y, Wang H, Qian J, Jin L, Wang X. A genetic variant of the NTCP gene is associated with HBV infection status in a Chinese population. Bmc Cancer. 16: 211. PMID 26968990 DOI: 10.1186/S12885-016-2257-6 |
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Yang M, Li L, Han H, Jin L, Jia D, Li S. Population data of 17 short tandem repeat loci in 2923 individuals from the Han population of Nantong in East China. International Journal of Legal Medicine. PMID 26932871 DOI: 10.1007/S00414-016-1332-5 |
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Feng Z, Xia M, Bao H, Wang L, Jin L, Li L, Li S. Genetic polymorphisms of 18 short tandem repeat loci in 3550 individuals from the Han population of Changchun, Northeast China. International Journal of Legal Medicine. PMID 26914803 DOI: 10.1007/S00414-016-1339-Y |
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Xu J, Li L, Wei L, Nie Z, Yang S, Xia M, Ma T, Sun H, Zhao X, Ping Y, Zhou H, Xue F, Zhao Z, Jin L, Li S. Genetic analysis of 17 Y-STR loci in Han population from Shandong Province in East China. Forensic Science International. Genetics. PMID 26857891 DOI: 10.1016/J.Fsigen.2016.01.016 |
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Zhang H, Yang S, Guo W, Ren B, Pu L, Ma T, Xia M, Jin L, Li L, Li S. Population genetic analysis of the GlobalFiler STR loci in 748 individuals from the Kazakh population of Xinjiang in northwest China. International Journal of Legal Medicine. PMID 26846763 DOI: 10.1007/S00414-016-1319-2 |
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Hou Z, Luo Y, Wang Z, Zheng HX, Wang Y, Zhou H, Wu L, Jin L. Inferring the Dynamics of Effective Population Size Using Autosomal Genomes. Scientific Reports. 6: 20079. PMID 26832887 DOI: 10.1038/Srep20079 |
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Zhu J, Wang M, He J, Zhu M, Wang JC, Jin L, Wang XF, Yang YJ, Xiang JQ, Wei Q. Polymorphisms in the AKT1 and AKT2 genes and oesophageal squamous cell carcinoma risk in an Eastern Chinese population. Journal of Cellular and Molecular Medicine. PMID 26828791 DOI: 10.1111/Jcmm.12750 |
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Wang MY, He J, Zhu ML, Teng XY, Li QX, Sun MH, Wang XF, Yang YJ, Wang JC, Jin L, Wang YN, Wei QY. A Functional Polymorphism (rs2494752) in the AKT1 Promoter Region and Gastric Adenocarcinoma Risk in an Eastern Chinese Population. Scientific Reports. 6: 20008. PMID 26818920 DOI: 10.1038/Srep20008 |
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Zhang H, Xia M, Qi L, Dong L, Song S, Ma T, Yang S, Jin L, Li L, Li S. Forensic and population genetic analysis of Xinjiang Uyghur population on 21 short tandem repeat loci of 6-dye GlobalFiler™ PCR Amplification kit. Forensic Science International. Genetics. 22: 22-24. PMID 26809046 DOI: 10.1016/J.Fsigen.2016.01.005 |
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Han Y, Li L, Liu X, Chen W, Yang S, Wei L, Xia M, Ma T, Jin L, Li S. Genetic analysis of 17 Y-STR loci in Han and Korean populations from Jilin Province, Northeast China. Forensic Science International. Genetics. 22: 8-10. PMID 26799315 DOI: 10.1016/J.Fsigen.2016.01.003 |
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Yao H, Wen S, Tong X, Zhou B, Du P, Shi M, Jin L, Li H. Y chromosomal clue successfully facilitated the arrest of Baiyin serial killer Chinese Science Bulletin. 61: 1715-1717. DOI: 10.1007/S11434-016-1183-Y |
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Li L, Yu G, Li S, Jin L, Yan S. Genetic analysis of 17 Y-STR loci from 1019 individuals of six Han populations in East China. Forensic Science International. Genetics. 20: 101-102. PMID 26529186 DOI: 10.1016/J.Fsigen.2015.10.007 |
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Qiu LX, He J, Cheng L, Zhou F, Wang MY, Sun MH, Zhou XY, Li J, Guo WJ, Wang YN, Yang YJ, Wang JC, Jin L, Zhu XD, Wei QY. Genetic variant of PRKAA1 and gastric cancer risk in an eastern chinese population. Oncotarget. PMID 26485766 DOI: 10.18632/Oncotarget.6124 |
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Sampson JN, Wheeler WA, Yeager M, Panagiotou O, Wang Z, Berndt SI, Lan Q, Abnet CC, Amundadottir LT, Figueroa JD, Landi MT, Mirabello L, Savage SA, Taylor PR, Vivo ID, ... ... Jin L, et al. Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for Thirteen Cancer Types. Journal of the National Cancer Institute. 107. PMID 26464424 DOI: 10.1093/Jnci/Djv279 |
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He Y, Wang M, Huang X, Li R, Xu H, Xu S, Jin L. A probabilistic method for testing and estimating selection differences between populations. Genome Research. PMID 26463656 DOI: 10.1101/Gr.192336.115 |
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Basang Z, Wang B, Li L, Yang L, Liu L, Cui C, Lanzi G, Yuzhen N, Duo J, Zheng H, Wang Y, Xu S, Jin L, Wang X. HIF2A Variants Were Associated with Different Levels of High-Altitude Hypoxia among Native Tibetans. Plos One. 10: e0137956. PMID 26368009 DOI: 10.1371/Journal.Pone.0137956 |
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Niu Z, Wang J, Zou H, Yang C, Huang W, Jin L. Common MIR146A Polymorphisms in Chinese Ankylosing Spondylitis Subjects and Controls. Plos One. 10: e0137770. PMID 26366721 DOI: 10.1371/Journal.Pone.0137770 |
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Shu L, Li L, Yu G, Yu B, Liu Y, Li S, Jin L, Yan S. Genetic analysis of 17 Y-STR loci in Han, Dong, Miao and Tujia populations from Hunan province, central-southern China. Forensic Science International. Genetics. 19: 250-251. PMID 26295934 DOI: 10.1016/J.Fsigen.2015.07.007 |
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Wang MY, Li QX, He J, Qiu LX, Wang YN, Li J, Sun MH, Wang XF, Yang YJ, Wang JC, Jin L, Wei QY. Genetic variations in the mTOR gene contribute toward gastric adenocarcinoma susceptibility in an Eastern Chinese population. Pharmacogenetics and Genomics. PMID 26287940 DOI: 10.1097/Fpc.0000000000000163 |
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Zou S, Sang Q, Wang H, Feng R, Li Q, Zhao X, Xing Q, Jin L, He L, Wang L. Common genetic variation in CYP1B1 is associated with concentrations of T₄, FT₃ and FT₄ in the sera of polycystic ovary syndrome patients. Molecular Biology Reports. 40: 3315-20. PMID 23283740 DOI: 10.1007/S11033-012-2406-1 |
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Jin W, Wang S, Wang H, Jin L, Xu S. Exploring population admixture dynamics via empirical and simulated genome-wide distribution of ancestral chromosomal segments. American Journal of Human Genetics. 91: 849-62. PMID 23103229 DOI: 10.1016/J.Ajhg.2012.09.008 |
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Zheng H, Yan S, Qin Z, Jin L. MtDNA analysis of global populations support that major population expansions began before Neolithic Time Scientific Reports. 2: 745-745. PMID 23082240 DOI: 10.1038/Srep00745 |
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Zhao JY, Yang XY, Shi KH, Sun SN, Hou J, Ye ZZ, Wang J, Duan WY, Qiao B, Chen YJ, Shen HB, Huang GY, Jin L, Wang HY. A functional variant in the cystathionine β-synthase gene promoter significantly reduces congenital heart disease susceptibility in a Han Chinese population. Cell Research. PMID 22986502 DOI: 10.1038/Cr.2012.135 |
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Zhang Y, Wang MY, He J, Wang JC, Yang YJ, Jin L, Chen ZY, Ma XJ, Sun MH, Xia KQ, Hong XN, Wei QY, Zhou XY. Tumor necrosis factor-α induced protein 8 polymorphism and risk of Non-Hodgkin's lymphoma in a Chinese population: A case-control study Plos One. 7. PMID 22666399 DOI: 10.1371/Journal.Pone.0037846 |
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Shi Y, Ding Y, Lei YP, Yang XY, Xie GM, Wen J, Cai CQ, Li H, Chen Y, Zhang T, Wu BL, Jin L, Chen YG, Wang HY. Identification of novel rare mutations of DACT1 in human neural tube defects. Human Mutation. 33: 1450-5. PMID 22610794 DOI: 10.1002/Humu.22121 |
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Liu Y, Li S, Chen X, Zheng L, Yang Y, Jin L, Wang X. Association of natriuretic peptide receptor-C gene with ischemic stroke and hypertension in Chinese Han population. Clinical and Experimental Hypertension (New York, N.Y. : 1993). 34: 504-9. PMID 22559095 DOI: 10.3109/10641963.2012.681719 |
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He Y, Wang WR, Xu S, Jin L. Paleolithic Contingent in Modern Japanese: Estimation and Inference using Genome-wide Data Scientific Reports. 2: 355-355. PMID 22482036 DOI: 10.1038/Srep00355 |
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Chen X, Yang Y, Li S, Peng Q, Zheng L, Jin L, Wang X. Several polymorphisms of KCNQ1 gene are associated with plasma lipid levels in general Chinese populations. Plos One. 7. PMID 22479571 DOI: 10.1371/Journal.Pone.0034229 |
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Li C, Xu J, Zhao S, Zhang S, Ma T, Zhao Z, Yang Y, Jin L, Li S. Genetic analysis of the 11 X-STR loci in Uigur population from China. Forensic Science International. Genetics. 6: e139-40. PMID 22436124 DOI: 10.1016/J.Fsigen.2012.02.008 |
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Xu S, Pugach I, Stoneking M, Kayser M, Jin L. Genetic dating indicates that the Asian-Papuan admixture through Eastern Indonesia corresponds to the Austronesian expansion. Proceedings of the National Academy of Sciences of the United States of America. 109: 4574-9. PMID 22396590 DOI: 10.1073/Pnas.1118892109 |
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Zhuang M, Yang Y, Cao F, Lu M, Wang X, Zhang J, Chen X, Cheng P, Zhang N, Ye W, Jin L. Associations of variants of CNR1 with obesity and obesity-related traits in Chinese women. Gene. 495: 194-8. PMID 22244745 DOI: 10.1016/J.Gene.2011.12.037 |
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Wang C, Yan S, Hou Z, Fu W, Xiong M, Han S, Jin L, Li H. Present Y chromosomes reveal the ancestry of Emperor CAO Cao of 1800 years ago. Journal of Human Genetics. 57: 216-8. PMID 22189622 DOI: 10.1038/Jhg.2011.147 |
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Zhao JY, Yang XY, Gong XH, Gu ZY, Duan WY, Wang J, Ye ZZ, Shen HB, Shi KH, Hou J, Huang GY, Jin L, Qiao B, Wang HY. Functional variant in methionine synthase reductase intron-1 significantly increases the risk of congenital heart disease in the Han Chinese population. Circulation. 125: 482-90. PMID 22179537 DOI: 10.1161/Circulationaha.111.050245 |
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Kang L, Lu Y, Wang C, Hu K, Chen F, Liu K, Li S, Jin L, Li H. Y-chromosome O3 haplogroup diversity in Sino-Tibetan populations reveals two migration routes into the eastern Himalayas. Annals of Human Genetics. 76: 92-9. PMID 22111786 DOI: 10.1111/J.1469-1809.2011.00690.X |
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Melé M, Javed A, Pybus M, Zalloua P, Haber M, Comas D, Netea MG, Balanovsky O, Balanovska E, Jin L, Yang Y, Pitchappan RM, Arunkumar G, Parida L, Calafell F, et al. Recombination gives a new insight in the effective population size and the history of the old world human populations. Molecular Biology and Evolution. 29: 25-30. PMID 21890475 DOI: 10.1093/Molbev/Msr213 |
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Jiang Y, Wang W, Wang J, Lu Y, Chen Y, Jin L, Lin D, He F, Wang H. Functional regulatory variants of MCL1 contribute to enhanced promoter activity and reduced risk of lung cancer in nonsmokers: implications for context-dependent phenotype of an antiapoptotic and antiproliferative gene in solid tumor. Cancer. 118: 2085-95. PMID 21887682 DOI: 10.1002/Cncr.26502 |
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Xu S, Jin L. Chromosome‐Wide Haplotype Sharing: A Measure Integrating Recombination Information to Reconstruct the Phylogeny of Human Populations Annals of Human Genetics. 75: 694-706. PMID 21972961 DOI: 10.1111/J.1469-1809.2011.00678.X |
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Cai X, Qin Z, Wen B, Xu S, Wang Y, Lu Y, Wei L, Wang C, Li S, Huang X, Jin L, Li H. Human migration through bottlenecks from Southeast Asia into East Asia during Last Glacial Maximum revealed by Y chromosomes. Plos One. 6: e24282. PMID 21904623 DOI: 10.1371/Journal.Pone.0024282 |
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He Y, Li C, Amos CI, Xiong M, Ling H, Jin L. Accelerating haplotype-based genome-wide association study using perfect phylogeny and phase-known reference data. Plos One. 6: e22097. PMID 21789217 DOI: 10.1371/Journal.Pone.0022097 |
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Wan XH, Li SJ, Cheng P, Zhang Q, Yang XC, Zhong GZ, Hu WL, Jin L, Wang XF. NINJ2 polymorphism is associated with ischemic stroke in Chinese Han population. Journal of the Neurological Sciences. 308: 67-71. PMID 21722921 DOI: 10.1016/J.Jns.2011.06.011 |
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Lin R, Wang X, Zhou W, Fu W, Wang Y, Huang W, Jin L. Association of a BLVRA common polymorphism with essential hypertension and blood pressure in Kazaks. Clinical and Experimental Hypertension (New York, N.Y. : 1993). 33: 294-8. PMID 21721974 DOI: 10.3109/10641963.2010.531854 |
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Li C, Ma T, Zhao S, Zhang S, Xu J, Zhao Z, Jin L, Li S. Development of 11 X-STR loci typing system and genetic analysis in Tibetan and Northern Han populations from China. International Journal of Legal Medicine. 125: 753-6. PMID 21717152 DOI: 10.1007/S00414-011-0592-3 |
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Siu H, Zhu Y, Jin L, Xiong M. Implication of next-generation sequencing on association studies. Bmc Genomics. 12: 322. PMID 21682891 DOI: 10.1186/1471-2164-12-322 |
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Yang Y, Zhou Y, Lu M, An Y, Li R, Chen Y, Lu DR, Jin L, Zhou WP, Qian J, Wang HY. Association between fibroblast growth factor receptor 4 polymorphisms and risk of hepatocellular carcinoma. Molecular Carcinogenesis. 51: 515-21. PMID 21656577 DOI: 10.1002/Mc.20805 |
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Zhu H, Shang D, Sun M, Choi S, Liu Q, Hao J, Figuera LE, Zhang F, Choy KW, Ao Y, Liu Y, Zhang XL, Yue F, Wang MR, Jin L, et al. X-linked congenital hypertrichosis syndrome is associated with interchromosomal insertions mediated by a human-specific palindrome near SOX3. American Journal of Human Genetics. 88: 819-26. PMID 21636067 DOI: 10.1016/J.Ajhg.2011.05.004 |
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Li H, Gu S, Han Y, Xu Z, Pakstis AJ, Jin L, Kidd JR, Kidd KK. Diversification of the ADH1B gene during expansion of modern humans. Annals of Human Genetics. 75: 497-507. PMID 21592108 DOI: 10.1111/J.1469-1809.2011.00651.X |
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Li X, Sun X, Jin L, Xue F. Worldwide spatial genetic structure of angiotensin-converting enzyme gene: a new evolutionary ecological evidence for the thrifty genotype hypothesis. European Journal of Human Genetics : Ejhg. 19: 1002-8. PMID 21559052 DOI: 10.1038/Ejhg.2011.66 |
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Fan W, Zhou K, Zhao Y, Wu W, Chen H, Jin L, Chen G, Shi J, Wei Q, Zhang T, Du G, Mao Y, Lu D, Zhou L. Possible association between genetic variants in the H2AFX promoter region and risk of adult glioma in a Chinese Han population. Journal of Neuro-Oncology. 105: 211-8. PMID 21512825 DOI: 10.1007/S11060-011-0586-5 |
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Yan S, Wang CC, Li H, Li SL, Jin L. An updated tree of Y-chromosome Haplogroup O and revised phylogenetic positions of mutations P164 and PK4. European Journal of Human Genetics : Ejhg. 19: 1013-5. PMID 21505448 DOI: 10.1038/Ejhg.2011.64 |
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Cao F, Wang X, Lu M, Yang Y, An Y, Zhang J, Chen X, Li L, Li S, Jiang J, Ye W, Jin L. Glucokinase regulatory protein (GCKR) gene rs4425043 polymorphism is associated with overweight and obesity in Chinese women. Lipids. 46: 357-63. PMID 21318467 DOI: 10.1007/S11745-011-3533-5 |
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Li R, Yang Y, An Y, Zhou Y, Liu Y, Yu Q, Lu D, Wang H, Jin L, Zhou W, Qian J, Shugart YY. Genetic polymorphisms in DNA double-strand break repair genes XRCC5, XRCC6 and susceptibility to hepatocellular carcinoma. Carcinogenesis. 32: 530-6. PMID 21304054 DOI: 10.1093/Carcin/Bgr018 |
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Lin R, Fu W, Zhou W, Wang Y, Wang X, Huang W, Jin L. Association of heme oxygenase-1 gene polymorphisms with essential hypertension and blood pressure in the Chinese Han population. Genetic Testing and Molecular Biomarkers. 15: 23-8. PMID 21275653 DOI: 10.1089/Gtmb.2010.0103 |
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Qiu YL, Wang W, Wang T, Sun P, Wu F, Zhu SM, Qian J, Jin L, Au W, Xia ZL. DNA repair gene polymorphisms and micronucleus frequencies in Chinese workers exposed to vinyl chloride monomer. International Journal of Hygiene and Environmental Health. 214: 225-30. PMID 21216194 DOI: 10.1016/J.Ijheh.2010.12.001 |
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Xu S, Li S, Yang Y, Tan J, Lou H, Jin W, Yang L, Pan X, Wang J, Shen Y, Wu B, Wang H, Jin L. A genome-wide search for signals of high-altitude adaptation in Tibetans. Molecular Biology and Evolution. 28: 1003-11. PMID 20961960 DOI: 10.1093/Molbev/Msq277 |
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Delfin F, Salvador JM, Calacal GC, Perdigon HB, Tabbada KA, Villamor LP, Halos SC, Gunnarsdóttir E, Myles S, Hughes DA, Xu S, Jin L, Lao O, Kayser M, Hurles ME, et al. The Y-chromosome landscape of the Philippines: extensive heterogeneity and varying genetic affinities of Negrito and non-Negrito groups. European Journal of Human Genetics : Ejhg. 19: 224-30. PMID 20877414 DOI: 10.1038/Ejhg.2010.162 |
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Zhong H, Shi H, Qi X, Duan Z, Tan P, Jin L, Su B, Ma RZ. Extended Y Chromosome Investigation Suggests Postglacial Migrations of Modern Humans into East Asia via the Northern Route Molecular Biology and Evolution. 28: 717-727. PMID 20837606 DOI: 10.1093/Molbev/Msq247 |
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Ke Y, Su B, Xiao J, Chen H, Huang W, Chen Z, Chu J, Tan J, Jin L, Lu D. Y-chromosome haplotype distribution in Han Chinese populations and modern human origin in East Asians. Science in China. Series C, Life Sciences. 44: 225-32. PMID 18726402 DOI: 10.1007/Bf02879329 |
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Chen X, Chen C, Jin L. Principal Component Analyses in Anthropological Genetics Advances in Anthropology. 1: 9-14. DOI: 10.4236/Aa.2011.12002 |
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Zhao J, Yang X, Gong X, Gu Z, Duan W, Wang J, Ye Z, Shen H, Shi K, Hou J, Huang G, Jin L, Qiao B, Wang H. A Functional Variant in MTRR Intron-1 Significantly Increases the Risk of Congenital Heart Disease in Han Chinese Population Circulation. 1. DOI: 10.1161/Circulationaha.111.Circulationaha.111.050245 |
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Xu S, Gupta S, Jin L. PEAS V1.0: a package for elementary analysis of SNP data. Molecular Ecology Resources. 10: 1085-1088. PMID 21565121 DOI: 10.1111/J.1755-0998.2010.02862.X |
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Lin R, Wang X, Zhou W, Fu W, Wang Y, Huang W, Jin L. Association of polymorphisms in the solute carrier organic anion transporter family member 1B1 gene with essential hypertension in the Uyghur population. Annals of Human Genetics. 75: 305-311. PMID 21309757 DOI: 10.1111/J.1469-1809.2010.00622.X |
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Fu W, Zhang F, Wang Y, Gu X, Jin L. Identification of copy number variation hotspots in human populations. American Journal of Human Genetics. 87: 494-504. PMID 20920665 DOI: 10.1016/J.Ajhg.2010.09.006 |
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Zhao YB, Li HJ, Li SN, Yu CC, Gao SZ, Xu Z, Jin L, Zhu H, Zhou H. Ancient DNA evidence supports the contribution of Di-Qiang people to the han Chinese gene pool. American Journal of Physical Anthropology. 144: 258-68. PMID 20872743 DOI: 10.1002/Ajpa.21399 |
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Xiao J, Liang Y, Li K, Zhou Y, Cai W, Zhou Y, Zhao Y, Xing Z, Chen G, Jin L. A novel strategy for genetic dissection of complex traits: the population of specific chromosome substitution strains from laboratory and wild mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 21: 370-6. PMID 20623355 DOI: 10.1007/S00335-010-9270-X |
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Li D, Sun Y, Lu Y, Mustavich LF, Ou C, Zhou Z, Li S, Jin L, Li H. Genetic origin of Kadai-speaking Gelong people on Hainan island viewed from Y chromosomes. Journal of Human Genetics. 55: 462-8. PMID 20485445 DOI: 10.1038/Jhg.2010.50 |
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Wang Y, Fu W, Xie F, Wang Y, Chu X, Wang H, Shen M, Wang Y, Wang Y, Sun W, Lei R, Yang L, Wu H, Foo J, Liu J, ... Jin L, et al. Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population. Journal of Human Genetics. 55: 490-4. PMID 20485444 DOI: 10.1038/Jhg.2010.53 |
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Zhang S, Lu J, Zhao X, Wu W, Wang H, Lu J, Wu Q, Chen X, Fan W, Chen H, Wang F, Hu Z, Jin L, Wei Q, Shen H, et al. A variant in the CHEK2 promoter at a methylation site relieves transcriptional repression and confers reduced risk of lung cancer. Carcinogenesis. 31: 1251-8. PMID 20462940 DOI: 10.1093/Carcin/Bgq089 |
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Zhong H, Shi H, Qi X, Xiao C, Jin L, Ma RZ, Su B. Global distribution of Y-chromosome haplogroup C reveals the prehistoric migration routes of African exodus and early settlement in East Asia Journal of Human Genetics. 55: 428-435. PMID 20448651 DOI: 10.1038/Jhg.2010.40 |
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Xu S, Kangwanpong D, Seielstad M, Srikummool M, Kampuansai J, Jin L. Genetic evidence supports linguistic affinity of Mlabri--a hunter-gatherer group in Thailand. Bmc Genetics. 11: 18-18. PMID 20302622 DOI: 10.1186/1471-2156-11-18 |
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Ji F, Wang W, Xia ZL, Zheng YJ, Qiu YL, Wu F, Miao WB, Jin RF, Qian J, Jin L, Zhu YL, Christiani DC. Prevalence and persistence of chromosomal damage and susceptible genotypes of metabolic and DNA repair genes in Chinese vinyl chloride-exposed workers. Carcinogenesis. 31: 648-53. PMID 20100738 DOI: 10.1093/Carcin/Bgq015 |
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Zhang HG, Chen YF, Ding M, Jin L, Case DT, Jiao YP, Wang XP, Bai CX, Jin G, Yang JM, Wang H, Yuan JB, Huang W, Wang ZG, Chen RB. Dermatoglyphics from all Chinese ethnic groups reveal geographic patterning. Plos One. 5: e8783. PMID 20098698 DOI: 10.1371/Journal.Pone.0008783 |
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Zhang F, Xu Z, Tan J, Sun Y, Xu B, Li S, Zhao X, Zhou H, Gong G, Zhang J, Jin L. Prehistorical East-West admixture of maternal lineages in a 2,500-year-old population in Xinjiang. American Journal of Physical Anthropology. 142: 314-20. PMID 20034008 DOI: 10.1002/Ajpa.21237 |
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Wang Z, Li Y, Wang B, He Y, Wang Y, Xi H, Li Y, Wang Y, Wang Y, Zhu D, Jin J, Huang W, Jin L. A haplotype of the catalase gene confers an increased risk of essential hypertension in Chinese Han. Human Mutation. 31: 272-8. PMID 20020532 DOI: 10.1002/Humu.21185 |
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Peng G, Luo L, Siu H, Zhu Y, Hu P, Hong S, Zhao J, Zhou X, Reveille JD, Jin L, Amos CI, Xiong M. Gene and pathway-based second-wave analysis of genome-wide association studies. European Journal of Human Genetics : Ejhg. 18: 111-7. PMID 19584899 DOI: 10.1038/Ejhg.2009.115 |
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Cao F, Han H, Wang F, Chen X, Lu M, Wang X, Lin R, Wen H, Jin L. [Study on the association between genetic polymorphism on WNK4 genes and essential hypertension among Kazakhs ethnic population, in Xinjiang]. Chinese Journal of Epidemiology. 31: 375-378. DOI: 10.3760/Cma.J.Issn.0254-6450.2010.04.004 |
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Zheng L, Sun H, Wang J, Li S, Bai J, Jin Y, Yu Y, Chen F, Jin L, Fu S. Y chromosomal STR polymorphism in northern Chinese populations. Biological Research. 42: 497-504. PMID 20140305 |
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Chen X, Wang H, Zhou G, Zhang X, Dong X, Zhi L, Jin L, He F. Molecular population genetics of human CYP3A locus: signatures of positive selection and implications for evolutionary environmental medicine. Environmental Health Perspectives. 117: 1541-1548. PMID 20019904 DOI: 10.1289/Ehp.0800528 |
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Xu S, Yin X, Li S, Jin W, Lou H, Yang L, Gong X, Wang H, Shen Y, Pan X, He Y, Yang Y, Wang Y, Fu W, An Y, ... Jin L, et al. Genomic dissection of population substructure of Han Chinese and its implication in association studies. American Journal of Human Genetics. 85: 762-74. PMID 19944404 DOI: 10.1016/J.Ajhg.2009.10.015 |
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Wang QS, Li YG, Chen XD, Yu JF, Wang J, Sun J, Lu SB, Jin L, Wang XF. Angiotensinogen polymorphisms and acquired atrial fibrillation in Chinese. Journal of Electrocardiology. 43: 373-7. PMID 19932491 DOI: 10.1016/J.Jelectrocard.2009.09.009 |
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Hua R, Xu JB, Wang JC, Zhu L, Li B, Liu Y, Huang SD, Jin L, Xu ZY, Wang XF. Association of TNFAIP3 polymorphism with rheumatic heart disease in Chinese Han population. Immunogenetics. 61: 739-44. PMID 19902201 DOI: 10.1007/S00251-009-0405-8 |
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Xu S, Jin W, Jin L. Haplotype-Sharing Analysis Showing Uyghurs Are Unlikely Genetic Donors Molecular Biology and Evolution. 26: 2197-2206. PMID 19564211 DOI: 10.1093/Molbev/Msp130 |
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Hu WL, Li SJ, Liu DT, Wang Y, Niu SQ, Yang XC, Zhang Q, Yu SZ, Jin L, Wang XF. Genetic variants on chromosome 9p21 and ischemic stroke in Chinese. Brain Research Bulletin. 79: 431-5. PMID 19559344 DOI: 10.1016/J.Brainresbull.2009.04.001 |
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He Y, Xu S, Jia C, Jin L. A design of multi-source samples as a shared control for association studies in genetically stratified populations Cell Research. 19: 913-915. PMID 19546887 DOI: 10.1038/Cr.2009.75 |
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Wang QS, Wang XF, Chen XD, Yu JF, Wang J, Sun J, Lu SB, Shen MY, Lu M, Li YG, Jin L. Genetic polymorphism of KCNH2 confers predisposition of acquired atrial fibrillation in Chinese. Journal of Cardiovascular Electrophysiology. 20: 1158-62. PMID 19490382 DOI: 10.1111/J.1540-8167.2009.01494.X |
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Li H, Borinskaya S, Yoshimura K, Kal'ina N, Marusin A, Stepanov VA, Qin Z, Khaliq S, Lee MY, Yang Y, Mohyuddin A, Gurwitz D, Mehdi SQ, Rogaev E, Jin L, et al. Refined geographic distribution of the oriental ALDH2*504Lys (nee 487Lys) variant. Annals of Human Genetics. 73: 335-45. PMID 19456322 DOI: 10.1111/J.1469-1809.2009.00517.X |
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Li SJ, Hu WL, Liu DT, Sun FH, Zhang Q, Yang XC, Yu SZ, Jin L, Wang XF. MTAP gene is associated with ischemic stroke in Chinese Hans. Journal of the Neurological Sciences. 284: 103-7. PMID 19427650 DOI: 10.1016/J.Jns.2009.04.013 |
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Zhou K, Liu Y, Zhang H, Liu H, Fan W, Zhong Y, Xu Z, Jin L, Wei Q, Huang F, Lu D, Zhou L. XRCC3 haplotypes and risk of gliomas in a Chinese population: a hospital-based case-control study. International Journal of Cancer. 124: 2948-53. PMID 19330829 DOI: 10.1002/Ijc.24307 |
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Lu M, Wang X, Wang F, Wang S, Lin R, Wang S, Wen H, Jin L. WNK4 polymorphisms and essential hypertension in the Uyghur population. Clinical and Experimental Hypertension (New York, N.Y. : 1993). 31: 179-85. PMID 19330605 DOI: 10.1080/10641960802621325 |
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Fu W, Wang Y, Wang Y, Li R, Lin R, Jin L. Missing call bias in high-throughput genotyping. Bmc Genomics. 10: 106. PMID 19284636 DOI: 10.1186/1471-2164-10-106 |
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Chu X, Dong C, Lei R, Sun L, Wang Z, Dong Y, Shen M, Wang Y, Wang B, Zhang K, Yang L, Li Y, Yuan W, Wang Y, Song H, ... Jin L, et al. Polymorphisms in the interleukin 3 gene show strong association with susceptibility to Graves' disease in Chinese population. Genes and Immunity. 10: 260-6. PMID 19262575 DOI: 10.1038/Gene.2009.3 |
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Lin R, Wang X, Wang Y, Zhang F, Wang Y, Fu W, Yu T, Li S, Xiong M, Huang W, Jin L. Association of polymorphisms in four bilirubin metabolism genes with serum bilirubin in three Asian populations. Human Mutation. 30: 609-15. PMID 19243019 DOI: 10.1002/Humu.20895 |
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Cheng X, Li H, Gupta S, Pan S, Hou J, Jin L. Dermatoglyphic changes during the population admixture between Kam and Han Chinese. Homo : Internationale Zeitschrift FüR Die Vergleichende Forschung Am Menschen. 60: 143-57. PMID 19167708 DOI: 10.1016/J.Jchb.2008.07.002 |
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Song HD, Liang J, Shi JY, Zhao SX, Liu Z, Zhao JJ, Peng YD, Gao GQ, Tao J, Pan CM, Shao L, Cheng F, Wang Y, Yuan GY, Xu C, ... ... Jin L, et al. Functional SNPs in the SCGB3A2 promoter are associated with susceptibility to Graves' disease. Human Molecular Genetics. 18: 1156-70. PMID 19126779 DOI: 10.1093/Hmg/Ddn442 |
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Li R, Shugart YY, Zhou W, An Y, Yang Y, Zhou Y, Zhang B, Lu D, Wang H, Qian J, Jin L. Common genetic variations of the cytochrome P450 1A1 gene and risk of hepatocellular carcinoma in a Chinese population. European Journal of Cancer (Oxford, England : 1990). 45: 1239-47. PMID 19110417 DOI: 10.1016/J.Ejca.2008.11.007 |
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Lu C, Zhang J, Li Y, Xia Y, Zhang F, Wu B, Wu W, Ji G, Gu A, Wang S, Jin L, Wang X. The b2/b3 subdeletion shows higher risk of spermatogenic failure and higher frequency of complete AZFc deletion than the gr/gr subdeletion in a Chinese population Human Molecular Genetics. 18: 1122-1130. PMID 19088127 DOI: 10.1093/Hmg/Ddn427 |
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Ma H, Hu Z, Wang H, Jin G, Wang Y, Sun W, Chen D, Tian T, Jin L, Wei Q, Lu D, Huang W, Shen H. ERCC6/CSB gene polymorphisms and lung cancer risk. Cancer Letters. 273: 172-6. PMID 18789574 DOI: 10.1016/J.Canlet.2008.08.002 |
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Qian J, Jing J, Jin G, Wang H, Wang Y, Liu H, Wang H, Li R, Fan W, An Y, Sun W, Wang Y, Ma H, Miao R, Hu Z, ... Jin L, et al. Association between polymorphisms in the GSTA4 gene and risk of lung cancer: a case-control study in a Southeastern Chinese population. Molecular Carcinogenesis. 48: 253-9. PMID 18767114 DOI: 10.1002/Mc.20478 |
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Zheng L, Sun H, Wang J, Li S, Bai J, Jin Y, Yu Y, Chen F, Jin L, Fu S. Y Chromosomal STR Polymorphism in Northern Chinese Populations Biological Research. 42: 497-504. DOI: 10.4067/S0716-97602009000400011 |
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Cao F, Chen X, Wang Q, Li L, Wang X, Lu M, Jin L. Associations of the genetic polymorphisms in CYP11B2 gene with nonfamilial structural atrial fibrillation Chinese Journal of Epidemiology. 30: 1069-1072. DOI: 10.3760/Cma.J.Issn.0254-6450.2009.010.022 |
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Xu L, Zhang F, Zhang DD, Chen XD, Lu M, Lin RY, Wen H, Jin L, Wang XF. OPRM1 gene is associated with BMI in Uyghur population. Obesity (Silver Spring, Md.). 17: 121-5. PMID 19008867 DOI: 10.1038/Oby.2008.504 |
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Shi H, Zhong H, Peng Y, Dong YL, Qi XB, Zhang F, Liu LF, Tan SJ, Ma RZ, Xiao CJ, Wells RS, Jin L, Su B. Y chromosome evidence of earliest modern human settlement in East Asia and multiple origins of Tibetan and Japanese populations. Bmc Biology. 6: 45. PMID 18959782 DOI: 10.1186/1741-7007-6-45 |
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Qiu Y, Wang W, Wang T, Liu J, Sun P, Qian J, Jin L, Xia Z. Genetic Polymorphisms, Messenger RNA Expression of p53, p21, and CCND1, and Possible Links with Chromosomal Aberrations in Chinese Vinyl Chloride–Exposed Workers Cancer Epidemiology, Biomarkers & Prevention. 17: 2578-2584. PMID 18842998 DOI: 10.1158/1055-9965.Epi-07-2925 |
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Xu Z, Zhang F, Xu B, Tan J, Li S, Li C, Zhou H, Zhu H, Zhang J, Duan Q, Jin L. Mitochondrial DNA evidence for a diversified origin of workers building First Emperor of China. Plos One. 3: e3275. PMID 18833341 DOI: 10.1371/Journal.Pone.0003275 |
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Xu S, Jin L. A Genome-wide Analysis of Admixture in Uyghurs and a High-Density Admixture Map for Disease-Gene Discovery American Journal of Human Genetics. 83: 322-336. PMID 18760393 DOI: 10.1016/J.Ajhg.2008.08.001 |
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Zhu W, Fan Z, Zhang C, Guo Z, Zhao Y, Zhou Y, Li K, Xing Z, Chen G, Liang Y, Jin L, Xiao J. A dominant X-linked QTL regulating pubertal timing in mice found by whole genome scanning and modified interval-specific congenic strain analysis. Plos One. 3: e3021. PMID 18725948 DOI: 10.1371/Journal.Pone.0003021 |
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Liu H, Jin G, Wang H, Wu W, Liu Y, Qian J, Fan W, Ma H, Miao R, Hu Z, Sun W, Wang Y, Jin L, Wei Q, Shen H, et al. Methyl-CpG binding domain 1 gene polymorphisms and lung cancer risk in a Chinese population. Biomarkers : Biochemical Indicators of Exposure, Response, and Susceptibility to Chemicals. 13: 607-17. PMID 18668384 DOI: 10.1080/13547500802168031 |
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He Y, Jiang R, Fu W, Bergen AW, Swan GE, Jin L. Correlation of population parameters leading to power differences in association studies with population stratification Annals of Human Genetics. 72: 801-811. PMID 18652602 DOI: 10.1111/J.1469-1809.2008.00465.X |
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Zhang J, Lin R, Wang F, Lu M, Lin RY, Wang SZ, Wen H, Jin L, Wang XF. A common polymorphism is associated with body mass index in Uyghur population. Diabetes Research and Clinical Practice. 81: e11-3. PMID 18514965 DOI: 10.1016/J.Diabres.2008.03.022 |
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Miao R, Gu H, Liu H, Hu Z, Jin G, Wang H, Wang Y, Sun W, Ma H, Chen D, Tian T, Jin L, Wei Q, Lu D, Huang W, et al. Tagging single nucleotide polymorphisms in MBD4 are associated with risk of lung cancer in a Chinese population. Lung Cancer (Amsterdam, Netherlands). 62: 281-6. PMID 18495292 DOI: 10.1016/J.Lungcan.2008.03.027 |
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Li H, Wen B, Chen SJ, Su B, Pramoonjago P, Liu Y, Pan S, Qin Z, Liu W, Cheng X, Yang N, Li X, Tran D, Lu D, Hsu MT, ... ... Jin L, et al. Paternal genetic affinity between Western Austronesians and Daic populations. Bmc Evolutionary Biology. 8: 146. PMID 18482451 DOI: 10.1186/1471-2148-8-146 |
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Li D, Li H, Ou C, Lu Y, Sun Y, Yang B, Qin Z, Zhou Z, Li S, Jin L. Paternal genetic structure of Hainan aborigines isolated at the entrance to East Asia. Plos One. 3: e2168. PMID 18478090 DOI: 10.1371/Journal.Pone.0002168 |
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Xu S, Huang W, Qian J, Jin L. Analysis of Genomic Admixture in Uyghur and Its Implication in Mapping Strategy American Journal of Human Genetics. 82: 883-894. PMID 18355773 DOI: 10.1016/J.Ajhg.2008.01.017 |
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Wang H, Liu Y, Tan W, Zhang Y, Zhao N, Jiang Y, Lin C, Hao B, Zhao D, Qian J, Lu D, Jin L, Wei Q, Lin D, He F. Association of the variable number of tandem repeats polymorphism in the promoter region of the SMYD3 gene with risk of esophageal squamous cell carcinoma in relation to tobacco smoking. Cancer Science. 99: 787-91. PMID 18294291 DOI: 10.1111/J.1349-7006.2008.00729.X |
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Wen H, Lin R, Jiao Y, Wang F, Wang S, Lu D, Qian J, Jin L, Wang X. Two polymorphisms in NEDD4L gene and essential hypertension in Chinese Hans - a population-based case-control study. Clinical and Experimental Hypertension (New York, N.Y. : 1993). 30: 87-94. PMID 18293164 DOI: 10.1080/10641960801949909 |
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Gan RJ, Pan SL, Mustavich LF, Qin ZD, Cai XY, Qian J, Liu CW, Peng JH, Li SL, Xu JS, Jin L, Li H. Pinghua population as an exception of Han Chinese's coherent genetic structure. Journal of Human Genetics. 53: 303-13. PMID 18270655 DOI: 10.1007/S10038-008-0250-X |
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Liu H, Jin G, Wang H, Wu W, Liu Y, Qian J, Fan W, Ma H, Miao R, Hu Z, Sun W, Wang Y, Jin L, Wei Q, Shen H, et al. Association of polymorphisms in one-carbon metabolizing genes and lung cancer risk: a case-control study in Chinese population. Lung Cancer (Amsterdam, Netherlands). 61: 21-9. PMID 18221821 DOI: 10.1016/J.Lungcan.2007.12.001 |
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Xue F, Wang Y, Xu S, Zhang F, Wen B, Wu X, Lu M, Deka R, Qian J, Jin L. A spatial analysis of genetic structure of human populations in China reveals distinct difference between maternal and paternal lineages. European Journal of Human Genetics : Ejhg. 16: 705-17. PMID 18212820 DOI: 10.1038/Sj.Ejhg.5201998 |
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Chen D, Jin G, Wang Y, Wang H, Liu H, Liu Y, Fan W, Ma H, Miao R, Hu Z, Sun W, Qian J, Jin L, Wei Q, Shen H, et al. Genetic variants in peroxisome proliferator-activated receptor-gamma gene are associated with risk of lung cancer in a Chinese population. Carcinogenesis. 29: 342-50. PMID 18187557 DOI: 10.1093/Carcin/Bgm285 |
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Jin G, Wang H, Hu Z, Liu H, Sun W, Ma H, Chen D, Miao R, Tian T, Jin L, Wei Q, Huang W, Lu D, Shen H. Potentially functional polymorphisms of EXO1 and risk of lung cancer in a Chinese population: A case-control analysis. Lung Cancer (Amsterdam, Netherlands). 60: 340-6. PMID 18079015 DOI: 10.1016/J.Lungcan.2007.11.003 |
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Wang X, Lin R, Wang S, Zhang L, Qian J, Lu D, Wen H, Jin L. Association study of variants in two ion-channel genes (TSC and CLCNKB) and hypertension in two ethnic groups in Northwest China. Clinica Chimica Acta. 388: 95-98. PMID 17997379 DOI: 10.1016/J.Cca.2007.10.017 |
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An Y, Jin G, Wang H, Wang Y, Liu H, Li R, Wang H, Qian J, Sun W, Wang Y, Ma H, Miao R, Hu Z, Jin L, Wei Q, et al. Polymorphisms in hMLH1 and risk of early-onset lung cancer in a southeast Chinese population. Lung Cancer (Amsterdam, Netherlands). 59: 164-70. PMID 17870204 DOI: 10.1016/J.Lungcan.2007.08.003 |
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Wu X, Jin L, Xiong M. Erratum: Composite measure of linkage disequilibrium for testing interaction between unlinked loci (European Journal of Human Genetics) (2008) vol. 16 (644-651) 10.1038/sj.ejhg.5202004) European Journal of Human Genetics. 16. DOI: 10.1038/Ejhg.2008.53 |
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Zhang Q, Zhang F, Chen XH, Wang YQ, Wang WQ, Lin AA, Cavalli-Sforza LL, Jin L, Huo R, Sha JH, Li Z, Su B. Rapid evolution, genetic variations, and functional association of the human spermatogenesis-related gene NYD-SP12. Journal of Molecular Evolution. 65: 154-61. PMID 17665087 DOI: 10.1007/S00239-006-0127-6 |
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Li H, Huang Y, Mustavich LF, Zhang F, Tan JZ, Wang LE, Qian J, Gao MH, Jin L. Y chromosomes of prehistoric people along the Yangtze River. Human Genetics. 122: 383-8. PMID 17657509 DOI: 10.1007/S00439-007-0407-2 |
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Xu S, Huang W, Wang H, He Y, Wang Y, Wang Y, Qian J, Xiong M, Jin L. Dissecting linkage disequilibrium in African-American genomes: roles of markers and individuals. Molecular Biology and Evolution. 24: 2049-58. PMID 17630283 DOI: 10.1093/Molbev/Msm135 |
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Wang H, Ding K, Zhang Y, Jin L, Kullo IJ, He F. Comparative and evolutionary pharmacogenetics of ABCB1: complex signatures of positive selection on coding and regulatory regions. Pharmacogenetics and Genomics. 17: 667-78. PMID 17622943 DOI: 10.1097/Fpc.0B013E328165249F |
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Lu C, Zhang F, Xia Y, Wu B, Gu A, Lu N, Wang S, Shen H, Jin L, Wang X. The association of Y chromosome haplogroups with spermatogenic failure in the Han Chinese. Journal of Human Genetics. 52: 659-663. PMID 17558462 DOI: 10.1007/S10038-007-0160-3 |
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Zhang F, Lu C, Li Z, Xie P, Xia Y, Zhu X, Wu B, Cai X, Wang X, Qian J, Wang X, Jin L. Partial deletions are associated with an increased risk of complete deletion in AZFc: a new insight into the role of partial AZFc deletions in male infertility. Journal of Medical Genetics. 44: 437-44. PMID 17412880 DOI: 10.1136/Jmg.2007.049056 |
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| 2007 |
Zhang F, Su B, Zhang Y, Jin L. Genetic studies of human diversity in East Asia Philosophical Transactions of the Royal Society B. 362: 987-996. PMID 17317646 DOI: 10.1098/Rstb.2007.2028 |
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Hu Z, Wang H, Shao M, Jin G, Sun W, Wang Y, Liu H, Wang Y, Ma H, Qian J, Jin L, Wei Q, Lu D, Huang W, Shen H. Genetic variants in MGMT and risk of lung cancer in Southeastern Chinese: a haplotype-based analysis. Human Mutation. 28: 431-40. PMID 17285603 DOI: 10.1002/Humu.20462 |
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Lĭ H, Pan S, Donnelly M, Tran D, Qin Z, Zhang Y, Cheng X, Yin R, Lin W, Hoang V, Pham V, Qian J, Jin L. Dermatoglyph Groups Kinh Vietnamese to Mon-Khmer International Journal of Anthropology. 21: 295-306. DOI: 10.1007/S11599-007-9033-6 |
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Zhao J, Jin L, Xiong M. Test for interaction between two unlinked loci. American Journal of Human Genetics. 79: 831-45. PMID 17033960 DOI: 10.1086/508571 |
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Gutala R, Carvalho-Silva DR, Jin L, Yngvadottir B, Avadhanula V, Nanne K, Singh L, Chakraborty R, Tyler-Smith C. A shared Y-chromosomal heritage between Muslims and Hindus in India. Human Genetics. 120: 543-51. PMID 16951948 DOI: 10.1007/S00439-006-0234-X |
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Hu Z, Xu L, Shao M, Yuan J, Wang Y, Wang F, Yuan W, Qian J, Ma H, Wang Y, Liu H, Chen W, Yang L, Jing G, Huo X, ... ... Jin L, et al. Polymorphisms in the two helicases ERCC2/XPD and ERCC3/XPB of the transcription factor IIH complex and risk of lung cancer: a case-control analysis in a Chinese population. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 15: 1336-40. PMID 16835333 DOI: 10.1158/1055-9965.Epi-06-0194 |
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Hu Z, Shao M, Yuan J, Xu L, Wang F, Wang Y, Yuan W, Qian J, Ma H, Wang Y, Liu H, Chen W, Yang L, Jin G, Huo X, ... ... Jin L, et al. Polymorphisms in DNA damage binding protein 2 (DDB2) and susceptibility of primary lung cancer in the Chinese: a case-control study. Carcinogenesis. 27: 1475-80. PMID 16522664 DOI: 10.1093/Carcin/Bgi350 |
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Huang W, He Y, Wang H, Wang Y, Liu Y, Wang Y, Chu X, Wang Y, Xu L, Shen Y, Xiong X, Li H, Wen B, Qian J, Yuan W, ... ... Jin L, et al. Linkage disequilibrium sharing and haplotype-tagged SNP portability between populations. Proceedings of the National Academy of Sciences of the United States of America. 103: 1418-21. PMID 16432195 DOI: 10.1073/Pnas.0510360103 |
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Bertoni B, Jin L, Chakraborty R, Sans M. Directional mating and a rapid male population expansion in a hybrid Uruguayan population. American Journal of Human Biology : the Official Journal of the Human Biology Council. 17: 801-8. PMID 16254907 DOI: 10.1002/Ajhb.20443 |
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Zhao JY, Xiong MM, Huang W, Wang H, Zuo J, Wu GD, Chen Z, Qiang BQ, Zhang ML, Chen JL, Ding W, Yuan WT, Xu HY, Jin L, Li YX, et al. An autosomal genomic scan for loci linked to type 2 diabetes in northern Han Chinese. Journal of Molecular Medicine (Berlin, Germany). 83: 209-15. PMID 15776287 DOI: 10.1007/S00109-004-0587-3 |
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Xie XH, Li H, Mao XY, Wen B, Gao S, Jin JZ, Lu DR, Jin L. [Genetic structure of Tujia as revealed by Y chromosomes]. Yi Chuan Xue Bao = Acta Genetica Sinica. 31: 1023-9. PMID 15552034 |
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Wen B, Li H, Gao S, Mao X, Gao Y, Li F, Zhang F, He Y, Dong Y, Zhang Y, Huang W, Jin J, Xiao C, Lu D, Chakraborty R, ... ... Jin L, et al. Genetic structure of Hmong-Mien speaking populations in East Asia as revealed by mtDNA lineages. Molecular Biology and Evolution. 22: 725-34. PMID 15548747 DOI: 10.1093/Molbev/Msi055 |
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Wen B, Li H, Lu D, Song X, Zhang F, He Y, Li F, Gao Y, Mao X, Zhang L, Qian J, Tan J, Jin J, Huang W, Deka R, ... ... Jin L, et al. Genetic evidence supports demic diffusion of Han culture. Nature. 431: 302-5. PMID 15372031 DOI: 10.1038/Nature02878 |
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| 2004 |
Wen B, Xie X, Gao S, Li H, Shi H, Song X, Qian T, Xiao C, Jin J, Su B, Lu D, Chakraborty R, Jin L. Analyses of genetic structure of Tibeto-Burman populations reveals sex-biased admixture in southern Tibeto-Burmans. American Journal of Human Genetics. 74: 856-65. PMID 15042512 DOI: 10.1086/386292 |
0.343 |
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| 2004 |
Li H, Pan WY, Wen B, Yang NN, Jin JZ, Jin L, Lu DR. [Origin of Hakka and Hakkanese: a genetics analysis]. Yi Chuan Xue Bao = Acta Genetica Sinica. 30: 873-80. PMID 14577381 |
0.387 |
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| 2003 |
Rudan I, Rudan D, Campbell H, Carothers A, Wright A, Smolej-Narancic N, Janicijevic B, Jin L, Chakraborty R, Deka R, Rudan P. Inbreeding and risk of late onset complex disease Journal of Medical Genetics. 40: 925-932. PMID 14684692 DOI: 10.1136/Jmg.40.12.925 |
0.3 |
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| 2003 |
Donadio FF, Siqueira MM, Vyse A, Jin L, Oliveira SA. The genomic analysis of rubella virus detected from outbreak and sporadic cases in Rio de Janeiro state, Brazil. Journal of Clinical Virology. 27: 205-209. PMID 12829043 DOI: 10.1016/S1386-6532(02)00270-6 |
0.316 |
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| 2003 |
Shi J, Xi H, Wang Y, Zhang C, Jiang Z, Zhang K, Shen Y, Jin L, Zhang K, Yuan W, Wang Y, Lin J, Hua Q, Wang F, Xu S, ... ... Jin L, et al. Divergence of the genes on human chromosome 21 between human and other hominoids and variation of substitution rates among transcription units. Proceedings of the National Academy of Sciences of the United States of America. 100: 8331-6. PMID 12826612 DOI: 10.1073/Pnas.1332748100 |
0.356 |
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| 2002 |
Wang N, Akey JM, Zhang K, Chakraborty R, Jin L. Distribution of recombination crossovers and the origin of haplotype blocks: the interplay of population history, recombination, and mutation. American Journal of Human Genetics. 71: 1227-34. PMID 12384857 DOI: 10.1086/344398 |
0.326 |
|
| 2001 |
Jiang Z, Akey JM, Shi J, Xiong M, Wang Y, Shen Y, Xu X, Chen H, Wu H, Xiao J, Lu D, Huang W, Jin L. A polymorphism in the promoter region of catalase is associated with blood pressure levels. Human Genetics. 109: 95-8. PMID 11479740 DOI: 10.1007/S004390100553 |
0.363 |
|
| 2001 |
Ke Y, Su B, Li H, Chen L, Qi C, Guo X, Huang W, Jin J, Lu D, Jin L. Y-chromosome evidence for no independent origin of modern human in China Chinese Science Bulletin. 46: 935-937. DOI: 10.1007/Bf02900470 |
0.349 |
|
| 2000 |
Xiao J, Hu F, Xu H, Su B, Jiang Y, Luo J, Zhang W, Tan J, Jin L, Lu D. Provincial distribution of three HIV-1 resistant polymorphisms (CCR5-Δ32, CCR2-64I, and SDF1-3′ A) in China. Science China-Life Sciences. 43: 16-20. PMID 18763111 DOI: 10.1007/Bf02881713 |
0.748 |
|
| 2000 |
Su B, Jin L, Underbill P, Martinson J, Saha N, McGarvey ST, Shriver MD, Chu J, Oefner P, Chakraborty R, Deka R. Polynesian origins: Insights from the Y chromosome Proceedings of the National Academy of Sciences of the United States of America. 97: 8225-8228. PMID 10899994 DOI: 10.1073/Pnas.97.15.8225 |
0.393 |
|
| 1999 |
Jin L, Beard S, Brown DWG. Genetic Heterogeneity of Mumps Virus in the United Kingdom: Identification of Two New Genotypes The Journal of Infectious Diseases. 180: 829-833. PMID 10438373 DOI: 10.1086/314957 |
0.302 |
|
| 1997 |
Shriver MD, Jin L, Ferrell RE, Deka R. Microsatellite data support an early population expansion in Africa Genome Research. 7: 586-591. PMID 9199931 DOI: 10.1101/Gr.7.6.586 |
0.333 |
|
| 1997 |
Jin L, Brown DW, Ramsay ME, Rota PA, Bellini WJ. The diversity of measles virus in the United Kingdom, 1992-1995. The Journal of General Virology. 1287-94. PMID 9191920 DOI: 10.1099/0022-1317-78-6-1287 |
0.3 |
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| 1994 |
Deka R, Shriver MD, Yu LM, Jin L, Aston CE, Chakraborty R, Ferrell RE. Conservation of human chromosome 13 polymorphic microsatellite (CA)n repeats in chimpanzees. Genomics. 22: 226-30. PMID 7959776 DOI: 10.1006/Geno.1994.1369 |
0.351 |
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| 1992 |
Chakraborty R, Deka R, Jin L, Ferrell RE. Allele sharing at six VNTR loci and genetic distances among three ethnically defined human populations. American Journal of Human Biology : the Official Journal of the Human Biology Council. 4: 387-397. PMID 28524310 DOI: 10.1002/Ajhb.1310040315 |
0.319 |
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