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

Year Number of Results
1963 1
1979 1
1981 1
1986 1
1988 3
1989 6
1990 3
1991 4
1992 2
1993 3
1994 3
1995 13
1996 4
1997 6
1998 9
1999 7
2000 16
2001 9
2002 20
2003 25
2004 26
2005 36
2006 33
2007 46
2008 64
2009 67
2010 105
2011 86
2012 131
2013 137
2014 132
2015 134
2016 101
2017 116
2018 120
2019 125
2020 123
2021 149
2022 129
2023 115
2024 118
2025 125
2026 45

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2,133 results

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Page 1
Unexplained Female Infertility Associated with Genetic Disease Variants.
Dougherty MP, Poch AM, Chorich LP, Hawkins ZA, Xu H, Roman RA, Liu H, Brakta S, Taylor HS, Knight J, Kim HG, Diamond MP, Layman LC. Dougherty MP, et al. Among authors: kim hg. N Engl J Med. 2023 Mar 16;388(11):1055-1056. doi: 10.1056/NEJMc2211539. N Engl J Med. 2023. PMID: 36920765 Free PMC article. No abstract available.
Response.
Gweon TG, Kim HG. Gweon TG, et al. Among authors: kim hg. Gastrointest Endosc. 2025 Apr;101(4):925-926. doi: 10.1016/j.gie.2024.11.028. Gastrointest Endosc. 2025. PMID: 40187865 No abstract available.
Delineation of a KDM2B-related neurodevelopmental disorder and its associated DNA methylation signature.
van Jaarsveld RH, Reilly J, Cornips MC, Hadders MA, Agolini E, Ahimaz P, Anyane-Yeboa K, Bellanger SA, van Binsbergen E, van den Boogaard MJ, Brischoux-Boucher E, Caylor RC, Ciolfi A, van Essen TAJ, Fontana P, Hopman S, Iascone M, Javier MM, Kamsteeg EJ, Kerkhof J, Kido J, Kim HG, Kleefstra T, Lonardo F, Lai A, Lev D, Levy MA, Lewis MES, Lichty A, Mannens MMAM, Matsumoto N, Maya I, McConkey H, Megarbane A, Michaud V, Miele E, Niceta M, Novelli A, Onesimo R, Pfundt R, Popp B, Prijoles E, Relator R, Redon S, Rots D, Rouault K, Saida K, Schieving J, Tartaglia M, Tenconi R, Uguen K, Verbeek N, Walsh CA, Yosovich K, Yuskaitis CJ, Zampino G, Sadikovic B, Alders M, Oegema R. van Jaarsveld RH, et al. Among authors: kim hg. Genet Med. 2023 Jan;25(1):49-62. doi: 10.1016/j.gim.2022.09.006. Epub 2022 Nov 1. Genet Med. 2023. PMID: 36322151 Free PMC article.
A programmed decline in ribosome levels governs human early neurodevelopment.
Ni C, Wei Y, Vona B, Park D, Wei Y, Schmitz DA, Ding Y, Sakurai M, Ballard E, Li L, Liu Y, Kumar A, Xing C, Qin S, Kim S, Foglizzo M, Zhao J, Kim HG, Ekmekci C, Karimiani EG, Imannezhad S, Eghbal F, Badv RS, Schwaibold EMC, Dehghani M, Mehrjardi MYV, Metanat Z, Eslamiyeh H, Khouj E, Alhajj SMN, Chedrawi A, Ramzan K, Hashmi JA, Alluqmani MM, Basit S, Veltra D, Marinakis NM, Niotakis G, Vorgia P, Sofocleous C, Lee H, Jeong WC, Umair M, Bilal M, Alves CAPF, Sieber M, Kruer M, Houlden H, Alkuraya FS, Zeqiraj E, Greenberg RA, Cenik C, Yu L, Maroofian R, Wu J, Buszczak M. Ni C, et al. Among authors: kim hg. Nat Cell Biol. 2025 Aug;27(8):1240-1255. doi: 10.1038/s41556-025-01708-8. Epub 2025 Aug 4. Nat Cell Biol. 2025. PMID: 40760247 Free PMC article.
De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.
Anderson EN, Drukewitz S, Kour S, Chimata AV, Rajan DS, Schönnagel S, Stals KL, Donnelly D, O'Sullivan S, Mantovani JF, Tan TY, Stark Z, Zacher P, Chatron N, Monin P, Drunat S, Vial Y, Latypova X, Levy J, Verloes A, Carter JN, Bonner DE, Shankar SP, Bernstein JA, Cohen JS, Comi A, Carere DA, Dyer LM, Mullegama SV, Sanchez-Lara PA, Grand K, Kim HG, Ben-Mahmoud A, Gospe SM Jr, Belles RS, Bellus G, Lichtenbelt KD, Oegema R, Rauch A, Ivanovski I, Mau-Them FT, Garde A, Rabin R, Pappas J, Bley AE, Bredow J, Wagner T, Decker E, Bergmann C, Domenach L, Margot H; Undiagnosed Diseases Network; Lemke JR, Jamra RA, Hentschel J, Mefford H, Singh A, Pandey UB, Platzer K. Anderson EN, et al. Among authors: kim hg. medRxiv [Preprint]. 2025 Apr 1:2025.03.31.25324695. doi: 10.1101/2025.03.31.25324695. medRxiv. 2025. Update in: Am J Hum Genet. 2026 Jan 8;113(1):100-116. doi: 10.1016/j.ajhg.2025.12.004. PMID: 40236430 Free PMC article. Updated. Preprint.
Totally laparoscopic versus laparoscopy-assisted distal gastrectomy: the KLASS-07: a randomized controlled trial.
Park SH, Lee CM, Hur H, Min JS, Ryu SW, Son YG, Chae HD, Jeong O, Jung MR, Choi CI, Song KY, Lee HH, Kim HG, Jee YS, Hwang SH, Lee MS, Kim KH, Seo SH, Jeong IH, Son MW, Kim CH, Yoo MW, Oh SJ, Kim JG, Hwang SH, Choi SI, Yang KS, Huang H, Park S. Park SH, et al. Among authors: kim hg. Int J Surg. 2024 Aug 1;110(8):4810-4820. doi: 10.1097/JS9.0000000000001543. Int J Surg. 2024. PMID: 38716987 Free PMC article. Clinical Trial.
Combination of dual JAK/HDAC inhibitor with regorafenib synergistically reduces tumor growth, metastasis, and regorafenib-induced toxicity in colorectal cancer.
Bajpai P, Agarwal S, Afaq F, Al Diffalha S, Chandrashekar DS, Kim HG, Shelton A, Miller CR, Singh SK, Singh R, Varambally S, Nagaraju GP, Manne A, Paluri R, Khushman M, Manne U. Bajpai P, et al. Among authors: kim hg. J Exp Clin Cancer Res. 2024 Jul 11;43(1):192. doi: 10.1186/s13046-024-03106-8. J Exp Clin Cancer Res. 2024. PMID: 38992681 Free PMC article.
De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.
Anderson EN, Drukewitz S, Kour S, Chimata AV, Rajan DS, Schönnagel S, Stals KL, Donnelly D, O'Sullivan S, Mantovani JF, Tan TY, Stark Z, Zacher P, Chatron N, Monin P, Drunat S, Vial Y, Latypova X, Levy J, Verloes A, Carter JN, Bonner DE, Shankar SP, Bernstein JA, Cohen JS, Comi A, Carere DA, Dyer LM, Mullegama SV, Sanchez-Lara PA, Grand K, Kim HG, Ben-Mahmoud A, Gospe SM Jr, Belles RS, Bellus G, Lichtenbelt KD, Oegema R, Rauch A, Ivanovski I, Mau-Them FT, Garde A, Rabin R, Pappas J, Bley AE, Bredow J, Wagner T, Decker E, Bergmann C, Domenach L, Margot H; Undiagnosed Diseases Network; Lemke JR, Abou Jamra R, Hentschel J, Mefford H, Singh A, Pandey UB, Platzer K. Anderson EN, et al. Among authors: kim hg. Am J Hum Genet. 2026 Jan 8;113(1):100-116. doi: 10.1016/j.ajhg.2025.12.004. Epub 2025 Dec 29. Am J Hum Genet. 2026. PMID: 41468891 Free PMC article.
2,133 results