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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 5
2004 2
2005 3
2006 4
2007 3
2008 9
2009 12
2010 14
2011 10
2012 13
2013 17
2014 29
2015 17
2016 20
2017 29
2018 31
2019 41
2020 39
2021 43
2022 57
2023 43
2024 53
2025 72
2026 33

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533 results

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Page 1
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.
Jin SC, Homsy J, Zaidi S, Lu Q, Morton S, DePalma SR, Zeng X, Qi H, Chang W, Sierant MC, Hung WC, Haider S, Zhang J, Knight J, Bjornson RD, Castaldi C, Tikhonoa IR, Bilguvar K, Mane SM, Sanders SJ, Mital S, Russell MW, Gaynor JW, Deanfield J, Giardini A, Porter GA Jr, Srivastava D, Lo CW, Shen Y, Watkins WS, Yandell M, Yost HJ, Tristani-Firouzi M, Newburger JW, Roberts AE, Kim R, Zhao H, Kaltman JR, Goldmuntz E, Chung WK, Seidman JG, Gelb BD, Seidman CE, Lifton RP, Brueckner M. Jin SC, et al. Among authors: zhang j. Nat Genet. 2017 Nov;49(11):1593-1601. doi: 10.1038/ng.3970. Epub 2017 Oct 9. Nat Genet. 2017. PMID: 28991257 Free PMC article.
Genomic analysis of 11,555 probands identifies 60 dominant congenital heart disease genes.
Sierant MC, Jin SC, Bilguvar K, Morton SU, Dong W, Jiang W, Lu Z, Li B, López-Giráldez F, Tikhonova I, Zeng X, Lu Q, Choi J, Zhang J, Nelson-Williams C, Knight JR, Zhao H, Cao J, Mane S, Sedore SC, Gruber PJ, Lek M, Goldmuntz E, Deanfield J, Giardini A, Mital S, Russell M, Gaynor JW, King E, Wagner M, Srivastava D, Shen Y, Bernstein D, Porter GA Jr, Newburger JW, Seidman JG, Roberts AE, Yandell M, Yost HJ, Tristani-Firouzi M, Kim R, Chung WK, Gelb BD, Seidman CE, Brueckner M, Lifton RP. Sierant MC, et al. Among authors: zhang j. Proc Natl Acad Sci U S A. 2025 Apr;122(13):e2420343122. doi: 10.1073/pnas.2420343122. Epub 2025 Mar 24. Proc Natl Acad Sci U S A. 2025. PMID: 40127276 Free PMC article.
Slipknot-gauged mechanical transmission and robotic operation.
Xue Y, Cao J, Feng T, Zhang K, Li S, Hu J, Guo H, Zhang J, Song Y, Wang Z, Wang L, Huang Q, Zhou H, Zhou F, Shen J, Fan Y, Wang Z, Li X, Wong JW, Chen Z, Ruan D, Miao Z, Zhang B, Zhou E, Gan L, Wang X, Cao E, Chen T, Zou W, Zhang J, Lu H, Zhang Q, Liu S, Dong H, Xiong S, Peng S, Wong TW, Chen Y, Li T, Chen M, Yang X, Yang W, Cai X. Xue Y, et al. Among authors: zhang j. Nature. 2025 Nov;647(8091):889-896. doi: 10.1038/s41586-025-09673-w. Epub 2025 Nov 26. Nature. 2025. PMID: 41299050 Free PMC article.
cGAS-like receptors drive a systemic STING-dependent host response in Drosophila.
Ai X, Deng H, Li X, Wei Z, Chen Y, Yin T, Zhang J, Huang J, Li H, Lin X, Tan L, Chen D, Zhang X, Zhang X, Meignin C, Imler JL, Cai H. Ai X, et al. Among authors: zhang j. Cell Rep. 2024 Dec 24;43(12):115081. doi: 10.1016/j.celrep.2024.115081. Epub 2024 Dec 16. Cell Rep. 2024. PMID: 39688951 Free article.
Genetic or therapeutic neutralization of ALK1 reduces LDL transcytosis and atherosclerosis in mice.
Lee S, Schleer H, Park H, Jang E, Boyer M, Tao B, Gamez-Mendez A, Singh A, Folta-Stogniew E, Zhang X, Qin L, Xiao X, Xu L, Zhang J, Hu X, Pashos E, Tellides G, Shaul PW, Lee WL, Fernandez-Hernando C, Eichmann A, Sessa WC. Lee S, et al. Among authors: zhang j. Nat Cardiovasc Res. 2023 May;2(5):438-448. doi: 10.1038/s44161-023-00266-2. Epub 2023 May 11. Nat Cardiovasc Res. 2023. PMID: 39196046 Free PMC article.
Mutation of key signaling regulators of cerebrovascular development in vein of Galen malformations.
Zhao S, Mekbib KY, van der Ent MA, Allington G, Prendergast A, Chau JE, Smith H, Shohfi J, Ocken J, Duran D, Furey CG, Hao LT, Duy PQ, Reeves BC, Zhang J, Nelson-Williams C, Chen D, Li B, Nottoli T, Bai S, Rolle M, Zeng X, Dong W, Fu PY, Wang YC, Mane S, Piwowarczyk P, Fehnel KP, See AP, Iskandar BJ, Aagaard-Kienitz B, Moyer QJ, Dennis E, Kiziltug E, Kundishora AJ, DeSpenza T Jr, Greenberg ABW, Kidanemariam SM, Hale AT, Johnston JM, Jackson EM, Storm PB, Lang SS, Butler WE, Carter BS, Chapman P, Stapleton CJ, Patel AB, Rodesch G, Smajda S, Berenstein A, Barak T, Erson-Omay EZ, Zhao H, Moreno-De-Luca A, Proctor MR, Smith ER, Orbach DB, Alper SL, Nicoli S, Boggon TJ, Lifton RP, Gunel M, King PD, Jin SC, Kahle KT. Zhao S, et al. Among authors: zhang j. Nat Commun. 2023 Nov 17;14(1):7452. doi: 10.1038/s41467-023-43062-z. Nat Commun. 2023. PMID: 37978175 Free PMC article.
Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.
Jin SC, Lewis SA, Bakhtiari S, Zeng X, Sierant MC, Shetty S, Nordlie SM, Elie A, Corbett MA, Norton BY, van Eyk CL, Haider S, Guida BS, Magee H, Liu J, Pastore S, Vincent JB, Brunstrom-Hernandez J, Papavasileiou A, Fahey MC, Berry JG, Harper K, Zhou C, Zhang J, Li B, Zhao H, Heim J, Webber DL, Frank MSB, Xia L, Xu Y, Zhu D, Zhang B, Sheth AH, Knight JR, Castaldi C, Tikhonova IR, López-Giráldez F, Keren B, Whalen S, Buratti J, Doummar D, Cho M, Retterer K, Millan F, Wang Y, Waugh JL, Rodan L, Cohen JS, Fatemi A, Lin AE, Phillips JP, Feyma T, MacLennan SC, Vaughan S, Crompton KE, Reid SM, Reddihough DS, Shang Q, Gao C, Novak I, Badawi N, Wilson YA, McIntyre SJ, Mane SM, Wang X, Amor DJ, Zarnescu DC, Lu Q, Xing Q, Zhu C, Bilguvar K, Padilla-Lopez S, Lifton RP, Gecz J, MacLennan AH, Kruer MC. Jin SC, et al. Among authors: zhang j. Nat Genet. 2020 Oct;52(10):1046-1056. doi: 10.1038/s41588-020-0695-1. Epub 2020 Sep 28. Nat Genet. 2020. PMID: 32989326 Free PMC article.
533 results