| Year |
Citation |
Score |
| 2024 |
Zhu X, Liu L, Tian S, Zhao G, Zhi E, Chen Q, Zhang F, Zhang A, Tang S, Liu C. Deleterious variant in FAM71D cause male infertility with asthenoteratospermia. Molecular Genetics and Genomics : Mgg. 299: 35. PMID 38489045 DOI: 10.1007/s00438-024-02117-6 |
0.456 |
|
| 2024 |
Gao Y, Liu L, Tian S, Liu C, Lv M, Wu H, Tang D, Song B, Shen Q, Xu Y, Zhou P, Wei Z, Zhang F, Cao Y, He X. Whole-exome sequencing identifies ADGB as a novel causative gene for male infertility in humans: from motility to fertilization. Andrology. PMID 38385883 DOI: 10.1111/andr.13605 |
0.381 |
|
| 2024 |
Wang Y, Chen J, Huang X, Wu B, Dai P, Zhang F, Li J, Wang L. Gene-knockout by iSTOP enables rapid reproductive disease modeling and phenotyping in germ cells of the founder generation. Science China. Life Sciences. PMID 38332217 DOI: 10.1007/s11427-023-2408-2 |
0.405 |
|
| 2023 |
Zhou Y, Wang Y, Chen J, Wu B, Tang S, Zhang F, Liu C, Wang L. Dnali1 is required for sperm motility and male fertility in mice. Basic and Clinical Andrology. 33: 32. PMID 37993789 DOI: 10.1186/s12610-023-00205-y |
0.326 |
|
| 2023 |
Wang Y, Huang X, Sun G, Chen J, Wu B, Luo J, Tang S, Dai P, Zhang F, Li J, Wang L. Coiled-coil domain-containing 38 is required for acrosome biogenesis and fibrous sheath assembly in mice. Journal of Genetics and Genomics = Yi Chuan Xue Bao. PMID 37709195 DOI: 10.1016/j.jgg.2023.09.002 |
0.319 |
|
| 2023 |
Zhou J, Zhang B, Zeb A, Ma A, Chen J, Zhao D, Rahim F, Khan R, Zhang H, Zhang Y, Khan I, Kakakhel MBS, Khan A, Shah W, Jiang X, ... Zhang F, et al. A recessive ACTL7A founder variant leads to male infertility due to acrosome detachment in Pakistani Pashtuns. Clinical Genetics. PMID 37286336 DOI: 10.1111/cge.14383 |
0.382 |
|
| 2023 |
Zhang Y, Huang X, Xu Q, Yu M, Shu M, Shan S, Fan Y, Li S, Tao C, Zhao Y, Ji J, Qin Y, Lu C, Xia Y, Zhang F. Homozygous nonsense variants of KCTD19 cause male infertility in humans and mice. Journal of Genetics and Genomics = Yi Chuan Xue Bao. PMID 37257643 DOI: 10.1016/j.jgg.2023.05.008 |
0.303 |
|
| 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, ... ... Zhang F, 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 |
0.781 |
|
| 2023 |
Luo W, Ke H, Tang S, Jiao X, Li Z, Zhao S, Zhang F, Guo T, Qin Y. Next-generation sequencing of 500 POI patients identified novel responsible monogenic and oligogenic variants. Journal of Ovarian Research. 16: 39. PMID 36793102 DOI: 10.1186/s13048-023-01104-6 |
0.313 |
|
| 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, ... Zhang F, et al. Landscape of pathogenic mutations in premature ovarian insufficiency. Nature Medicine. PMID 36732629 DOI: 10.1038/s41591-022-02194-3 |
0.432 |
|
| 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, ... Zhang F, 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 |
0.789 |
|
| 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, ... Zhang F, 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 |
0.803 |
|
| 2022 |
Zheng H, Mei S, Li F, Wei L, Wang Y, Huang J, Zhang F, Huang J, Liu Y, Gu W, Liu H. Expansion of the mutation spectrum and phenotype of -related neurodevelopmental disorder. Frontiers in Molecular Neuroscience. 15: 970649. PMID 36466803 DOI: 10.3389/fnmol.2022.970649 |
0.329 |
|
| 2022 |
Liu L, Tang SY, Zhang F, Jiang F. A novel homozygous loss-of-function mutation in induces male infertility with nonobstructive azoospermia. Asian Journal of Andrology. PMID 36153927 DOI: 10.4103/aja202272 |
0.303 |
|
| 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 |
0.382 |
|
| 2022 |
Khan A, Tian S, Tariq M, Khan S, Safeer M, Ullah N, Akbar N, Javed I, Asif M, Ahmad I, Ullah S, Satti HS, Khan R, Naeem M, Ali M, ... ... Zhang F, et al. NGS-driven molecular diagnosis of heterogeneous hereditary neurological disorders reveals novel and known variants in disease-causing genes. Molecular Genetics and Genomics : Mgg. PMID 36002593 DOI: 10.1007/s00438-022-01945-8 |
0.773 |
|
| 2022 |
Yang C, Lin X, Ji Z, Huang Y, Zhang L, Luo J, Chen H, Li P, Tian R, Zhi E, Hong Y, Zhou Z, Zhang F, Li Z, Yao C. Novel bi-allelic variants in KASH5 are associated with meiotic arrest and non-obstructive azoospermia. Molecular Human Reproduction. PMID 35674372 DOI: 10.1093/molehr/gaac021 |
0.34 |
|
| 2022 |
Qin Y, Du Y, Chen L, Liu Y, Xu W, Liu Y, Li Y, Leng J, Wang Y, Zhang XY, Feng J, Zhang F, Jin L, Qiu Z, Gong X, et al. Correction: A recurrent SHANK1 mutation implicated in autism spectrum disorder causes autistic-like core behaviors in mice via downregulation of mGluR1-IP3R1-calcium signaling. Molecular Psychiatry. PMID 35538194 DOI: 10.1038/s41380-022-01605-8 |
0.303 |
|
| 2022 |
Zhang F. "Progressive motility" in elucidating novel genetic causes of male infertility. Asian Journal of Andrology. 24: 229-230. PMID 35532567 DOI: 10.4103/aja202231 |
0.322 |
|
| 2022 |
Qin Y, Du Y, Chen L, Liu Y, Xu W, Liu Y, Li Y, Leng J, Wang Y, Zhang XY, Feng J, Zhang F, Jin L, Qiu Z, Gong X, et al. A recurrent SHANK1 mutation implicated in autism spectrum disorder causes autistic-like core behaviors in mice via downregulation of mGluR1-IP3R1-calcium signaling. Molecular Psychiatry. PMID 35388181 DOI: 10.1038/s41380-022-01539-1 |
0.361 |
|
| 2022 |
Zhang X, Wang L, Ma Y, Wang Y, Liu H, Liu M, Qin L, Li J, Jiang C, Zhang X, Shan X, Liu Y, Li J, Li Y, Zheng R, ... ... Zhang F, et al. CEP128 is involved in spermatogenesis in humans and mice. Nature Communications. 13: 1395. PMID 35296684 DOI: 10.1038/s41467-022-29109-7 |
0.336 |
|
| 2022 |
Cong J, Yang Y, Wang X, Shen Y, Qi HT, Liu C, Tang S, Wu S, Tian S, Zhou Y, He X, Wang L, Liu MF, Zhang F. Deficiency of X-linked TENT5D causes male infertility by disrupting the mRNA stability during spermatogenesis. Cell Discovery. 8: 23. PMID 35256600 DOI: 10.1038/s41421-021-00369-9 |
0.737 |
|
| 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 |
0.807 |
|
| 2022 |
Lv M, Liu C, Ma C, Yu H, Shao Z, Gao Y, Liu Y, Wu H, Tang D, Tan Q, Zhang J, Li K, Xu C, Geng H, Zhang J, ... ... Zhang F, et al. Homozygous mutation in SLO3 leads to severe asthenoteratozoospermia due to acrosome hypoplasia and mitochondrial sheath malformations. Reproductive Biology and Endocrinology : Rb&E. 20: 5. PMID 34980136 DOI: 10.1186/s12958-021-00880-4 |
0.348 |
|
| 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 |
0.404 |
|
| 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, ... ... Zhang F, 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 |
0.804 |
|
| 2021 |
Tu C, Cong J, Zhang Q, He X, Zheng R, Yang X, Gao Y, Wu H, Lv M, Gu Y, Lu S, Liu C, Tian S, Meng L, Wang W, ... ... Zhang F, et al. Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice. American Journal of Human Genetics. PMID 34237282 DOI: 10.1016/j.ajhg.2021.06.010 |
0.822 |
|
| 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 |
0.821 |
|
| 2021 |
Zhou Z, Yang X, Pan Y, Shang L, Chen S, Yang J, Jin L, Zhang F, Wu Y. Temporal transcriptomic landscape of postnatal mouse ovaries reveals dynamic gene signatures associated with ovarian aging. Human Molecular Genetics. PMID 34137841 DOI: 10.1093/hmg/ddab163 |
0.373 |
|
| 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, ... ... Zhang F, 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 |
0.402 |
|
| 2021 |
Gao Y, Tian S, Sha Y, Zha X, Cheng H, Wang A, Liu C, Lv M, Ni X, Li Q, Wu H, Tan Q, Tang D, Song B, Ding D, ... ... Zhang F, et al. Novel bi-allelic variants in DNAH2 cause severe asthenoteratozoospermia with multiple morphological abnormalities of the flagella. Reproductive Biomedicine Online. PMID 33771466 DOI: 10.1016/j.rbmo.2021.01.011 |
0.781 |
|
| 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, ... ... Zhang F, 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 |
0.834 |
|
| 2021 |
Chen N, Zhao S, Jolly A, Wang L, Pan H, Yuan J, Chen S, Koch A, Ma C, Tian W, Jia Z, Kang J, Zhao L, Qin C, Fan X, ... ... Zhang F, et al. Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome. American Journal of Human Genetics. PMID 33434492 DOI: 10.1016/j.ajhg.2020.12.014 |
0.478 |
|
| 2020 |
Zhang B, Khan I, Liu C, Ma A, Khan A, Zhang Y, Huan Z, Kakakhel MBS, Zhou J, Zhang W, Li Y, Ali A, Jiang X, Murtaza G, Khan R, ... ... Zhang F, et al. Novel loss-of-function variants in DNAH17 cause multiple morphological abnormalities of the sperm flagella in humans and mice. Clinical Genetics. PMID 33070343 DOI: 10.1111/cge.13866 |
0.349 |
|
| 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 |
0.474 |
|
| 2020 |
Xin A, Qu R, Chen G, Zhang L, Chen J, Tao C, Fu J, Tang J, Ru Y, Chen Y, Peng X, Shi H, Zhang F, Sun X. Disruption in causes acrosomal ultrastructural defects in human and mouse sperm as a novel male factor inducing early embryonic arrest. Science Advances. 6: eaaz4796. PMID 32923619 DOI: 10.1126/Sciadv.Aaz4796 |
0.368 |
|
| 2020 |
Yao C, Yang C, Zhao L, Li P, Tian R, Chen H, Guo Y, Huang Y, Zhi E, Zhai J, Sun H, Zhang J, Hong Y, Zhang L, Ji Z, ... Zhang F, et al. Bi-allelic loss-of-function mutations cause meiotic arrest and non-obstructive azoospermia. Journal of Medical Genetics. PMID 32900840 DOI: 10.1136/Jmedgenet-2020-107042 |
0.349 |
|
| 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 |
0.427 |
|
| 2020 |
Gao L, Altae-Tran H, Böhning F, Makarova KS, Segel M, Schmid-Burgk JL, Koob J, Wolf YI, Koonin EV, Zhang F. Diverse enzymatic activities mediate antiviral immunity in prokaryotes. Science (New York, N.Y.). 369: 1077-1084. PMID 32855333 DOI: 10.1126/Science.Aba0372 |
0.323 |
|
| 2020 |
Li P, Ning Y, Wang W, Guo X, Poulet B, Wang X, Wen Y, Han J, Hao J, Liang X, Liu L, Du Y, Cheng B, Cheng S, Zhang L, ... ... Zhang F, et al. The integrative analysis of DNA methylation and mRNA expression profiles confirmed the role of selenocompound metabolism pathway in Kashin-Beck disease. Cell Cycle (Georgetown, Tex.). 1-16. PMID 32816579 DOI: 10.1080/15384101.2020.1807665 |
0.307 |
|
| 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, ... ... Zhang F, 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 |
0.817 |
|
| 2020 |
Weiss T, Wang C, Kang X, Zhao H, Gamo ME, Starker CG, Crisp PA, Zhou P, Springer NM, Voytas DF, Zhang F. Optimization of multiplexed CRISPR/Cas9 system for highly efficient genome editing in Setaria viridis. The Plant Journal : For Cell and Molecular Biology. PMID 32786122 DOI: 10.1111/Tpj.14949 |
0.367 |
|
| 2020 |
Cheng B, Qi X, Liang C, Zhang L, Ma M, Li P, Liu L, Cheng S, Yao Y, Chu X, Ye J, Wen Y, Jia Y, Zhang F. Integrative Genomic Enrichment Analysis Identified the Brain Regions and Development Stages Related to Anorexia Nervosa and Obsessive-Compulsive Disorder. Cerebral Cortex (New York, N.Y. : 1991). PMID 32770201 DOI: 10.1093/Cercor/Bhaa214 |
0.303 |
|
| 2020 |
Jin S, Fei H, Zhu Z, Luo Y, Liu J, Gao S, Zhang F, Chen YH, Wang Y, Gao C. Rationally Designed APOBEC3B Cytosine Base Editors with Improved Specificity. Molecular Cell. PMID 32721385 DOI: 10.1016/J.Molcel.2020.07.005 |
0.323 |
|
| 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 |
0.552 |
|
| 2020 |
Cheng B, Ning Y, Liang C, Li P, Liu L, Cheng S, Ma M, Zhang L, Xin Q, Wen Y, Zhang F. Genome-Wide Association Analysis Identified ANXA1 Associated with Shoulder Impingement Syndrome in UK Biobank Samples. G3 (Bethesda, Md.). PMID 32690583 DOI: 10.1534/G3.120.401257 |
0.318 |
|
| 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, ... ... Zhang F, 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 |
0.824 |
|
| 2020 |
Gussow AB, Auslander N, Faure G, Wolf YI, Zhang F, Koonin EV. Genomic determinants of pathogenicity in SARS-CoV-2 and other human coronaviruses. Proceedings of the National Academy of Sciences of the United States of America. PMID 32522874 DOI: 10.1073/Pnas.2008176117 |
0.312 |
|
| 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, ... ... Zhang F, 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 |
0.568 |
|
| 2020 |
Qi X, Yu F, Wen Y, Li P, Cheng B, Ma M, Cheng S, Zhang L, Liang C, Liu L, Zhang F. Integration of transcriptome-wide association study and messenger RNA expression profile to identify genes associated with osteoarthritis. Bone & Joint Research. 9: 130-138. PMID 32435465 DOI: 10.1302/2046-3758.93.Bjr-2019-0137.R1 |
0.324 |
|
| 2020 |
Zhao S, Zhang Y, Chen W, Li W, Wang S, Wang L, Zhao Y, Lin M, Ye Y, Lin J, Zheng Y, Liu J, Zhao H, Yan Z, Yang Y, ... ... Zhang F, et al. Diagnostic yield and clinical impact of exome sequencing in early-onset scoliosis (EOS). Journal of Medical Genetics. PMID 32381727 DOI: 10.1136/Jmedgenet-2019-106823 |
0.329 |
|
| 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 |
0.53 |
|
| 2020 |
Ni X, Wang J, Lv M, Liu C, Zhong Y, Tian S, Wu H, Cheng H, Gao Y, Tan Q, Chen B, Li Q, Song B, Wei Z, Zhou P, ... ... Zhang F, et al. A novel homozygous mutation in WDR19 induces disorganization of microtubules in sperm flagella and nonsyndromic asthenoteratospermia. Journal of Assisted Reproduction and Genetics. PMID 32323121 DOI: 10.1007/S10815-020-01770-1 |
0.792 |
|
| 2020 |
Wu H, Gao Y, Ma C, Shen Q, Wang J, Lv M, Liu C, Cheng H, Zhu F, Tian S, Elshewy N, Ni X, Tan Q, Xu X, Zhou P, ... ... Zhang F, et al. A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferens. Journal of Assisted Reproduction and Genetics. PMID 32314195 DOI: 10.1007/S10815-020-01779-6 |
0.781 |
|
| 2020 |
Schmid-Burgk JL, Gao L, Li D, Gardner Z, Strecker J, Lash B, Zhang F. Highly Parallel Profiling of Cas9 Variant Specificity. Molecular Cell. PMID 32187529 DOI: 10.1016/J.Molcel.2020.02.023 |
0.356 |
|
| 2020 |
Cheng B, Liang C, Li P, Liu L, Cheng S, Ma M, Zhang L, Qi X, Wen Y, Zhang F. Evaluating the Genetic Correlations Between Left-Handedness and Mental Disorder Using Linkage Disequilibrium Score Regression and Transcriptome-Wide Association Study. Biochemical Genetics. PMID 32100139 DOI: 10.1007/S10528-020-09952-3 |
0.337 |
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| 2020 |
Sun X, Ding Y, Orr MC, Zhang F. Streamlining universal single-copy ortholog and ultraconserved element design: a case study in Collembola. Molecular Ecology Resources. PMID 32065730 DOI: 10.1111/1755-0998.13146 |
0.344 |
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| 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, ... ... Zhang F, et al. Homozygous mutations in can induce asthenoteratospermia with severe MMAF. Journal of Medical Genetics. PMID 32051257 DOI: 10.1136/Jmedgenet-2019-106479 |
0.551 |
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| 2020 |
Qi X, Wen Y, Li P, Liang C, Cheng B, Ma M, Cheng S, Zhang L, Liu L, Kafle OP, Zhang F. An integrative analysis of genome-wide association study and regulatory SNP annotation datasets identified candidate genes for bipolar disorder. International Journal of Bipolar Disorders. 8: 6. PMID 32009227 DOI: 10.1186/S40345-019-0170-Z |
0.308 |
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| 2020 |
Cheng S, Ma M, Zhang L, Liu L, Cheng B, Qi X, Liang C, Li P, Kafle OP, Wen Y, Zhang F. CGSEA: A Flexible Tool for Evaluating the Associations of Chemicals with Complex Diseases. G3 (Bethesda, Md.). PMID 31937547 DOI: 10.1534/G3.119.400945 |
0.318 |
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| 2019 |
Xie Y, Wang Q, Gao N, Wu F, Lan F, Zhang F, Jin L, Huang Z, Ge J, Wang H, Wang Y. MircroRNA-10b Promotes Human Embryonic Stem Cell-Derived Cardiomyocyte Proliferation via Novel Target Gene LATS1. Molecular Therapy. Nucleic Acids. 19: 437-445. PMID 31902743 DOI: 10.1016/J.Omtn.2019.11.026 |
0.34 |
|
| 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, ... ... Zhang F, 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 |
0.562 |
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| 2019 |
El-Battrawy I, Müller J, Zhao Z, Cyganek L, Zhong R, Zhang F, Kleinsorge M, Lan H, Li X, Xu Q, Huang M, Liao Z, Moscu-Gregor A, Albers S, Dinkel H, et al. Studying Brugada Syndrome With an SCN1B Variants in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes. Frontiers in Cell and Developmental Biology. 7: 261. PMID 31737628 DOI: 10.3389/fcell.2019.00261 |
0.306 |
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| 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, ... ... Zhang F, 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 |
0.821 |
|
| 2019 |
Zetsche B, Strecker J, Abudayyeh OO, Gootenberg JS, Scott DA, Zhang F. A Survey of Genome Editing Activity for 16 Cas12a Orthologs. The Keio Journal of Medicine. PMID 31723075 DOI: 10.2302/Kjm.2019-0009-Oa |
0.304 |
|
| 2019 |
Zhang B, Ma H, Khan T, Ma A, Li T, Zhang H, Gao J, Zhou J, Li Y, Yu C, Bao J, Ali A, Murtaza G, Yin H, Gao Q, ... ... Zhang F, et al. A missense variant causes flagella destabilization and asthenozoospermia. The Journal of Experimental Medicine. PMID 31658987 DOI: 10.1084/Jem.20182365 |
0.398 |
|
| 2019 |
Zhang L, Du Y, Wen Y, Ma M, Cheng S, Cheng B, Li P, Qi X, Liang C, Liu L, Liang X, Guo X, Zhang F. Integrating transcriptome-wide association study and mRNA expression profiling identified candidate genes and pathways associated with osteomyelitis. Scandinavian Journal of Rheumatology. 1-6. PMID 31657276 DOI: 10.1080/03009742.2019.1653492 |
0.333 |
|
| 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 |
0.346 |
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| 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, et al. Rare variants in FANCA induce premature ovarian insufficiency. Human Genetics. PMID 31535215 DOI: 10.1007/S00439-019-02059-9 |
0.587 |
|
| 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, ... ... Zhang F, 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 |
0.816 |
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Yang G, Zhang F, Hancock CN, Wessler SR. Transposition of the rice miniature inverted repeat transposable element mPing in Arabidopsis thaliana. Proceedings of the National Academy of Sciences of the United States of America. 104: 10962-7. PMID 17578919 DOI: 10.1073/Pnas.0702080104 |
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| 2007 |
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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Chen Y, Xiong DH, Yang TL, Yang F, Jiang H, Zhang F, Shen H, Xiao P, Recker RR, Deng HW. Variations in RANK gene are associated with adult height in Caucasians. American Journal of Human Biology : the Official Journal of the Human Biology Council. 19: 559-65. PMID 17546619 DOI: 10.1002/Ajhb.20619 |
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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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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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Zhang J, Zhang F, Peterson T. Transposition of reversed Ac element ends generates novel chimeric genes in maize. Plos Genetics. 2: e164. PMID 17029561 DOI: 10.1371/Journal.Pgen.0020164 |
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Zhang F, Peterson T. Gene conversion between direct noncoding repeats promotes genetic and phenotypic diversity at a regulatory locus of Zea mays (L.). Genetics. 174: 753-62. PMID 16816430 DOI: 10.1534/Genetics.105.053942 |
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Zhang F, Li Z, Wen B, Jiang J, Shao M, Zhao Y, He Y, Song X, Qian J, Lu D, Jin L. A frequent partial AZFc deletion does not render an increased risk of spermatogenic impairment in East Asians. Annals of Human Genetics. 70: 304-13. PMID 16674553 DOI: 10.1111/J.1529-8817.2005.00231.X |
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