Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
2003 1
2006 1
2007 3
2008 5
2009 1
2010 5
2011 4
2012 3
2013 6
2014 7
2015 9
2016 11
2017 6
2018 5
2019 5
2020 7
2021 4
2022 8
2023 14
2024 5

Text availability

Article attribute

Article type

Publication date

Search Results

101 results

Results by year

Filters applied: . Clear all
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.
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.
Multi-timescale reinforcement learning in the brain.
Masset P, Tano P, Kim HR, Malik AN, Pouget A, Uchida N. Masset P, et al. bioRxiv [Preprint]. 2023 Nov 14:2023.11.12.566754. doi: 10.1101/2023.11.12.566754. bioRxiv. 2023. PMID: 38014166 Free PMC article. Preprint.
The neural basis of depth perception from motion parallax.
Kim HR, Angelaki DE, DeAngelis GC. Kim HR, et al. Philos Trans R Soc Lond B Biol Sci. 2016 Jun 19;371(1697):20150256. doi: 10.1098/rstb.2015.0256. Philos Trans R Soc Lond B Biol Sci. 2016. PMID: 27269599 Free PMC article. Review.
Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function.
Lin SJ, Vona B, Porter HM, Izadi M, Huang K, Lacassie Y, Rosenfeld JA, Khan S, Petree C, Ali TA, Muhammad N, Khan SA, Muhammad N, Liu P, Haymon ML, Rüschendorf F, Kong IK, Schnapp L, Shur N, Chorich L, Layman L, Haaf T, Pourkarimi E, Kim HG, Varshney GK. Lin SJ, et al. Among authors: kim hg. Hum Mutat. 2022 Oct;43(10):1472-1489. doi: 10.1002/humu.24435. Epub 2022 Jul 21. Hum Mutat. 2022. PMID: 35815345
The role of state uncertainty in the dynamics of dopamine.
Mikhael JG, Kim HR, Uchida N, Gershman SJ. Mikhael JG, et al. Curr Biol. 2022 Mar 14;32(5):1077-1087.e9. doi: 10.1016/j.cub.2022.01.025. Epub 2022 Feb 2. Curr Biol. 2022. PMID: 35114098 Free PMC article.
Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly.
Uctepe E, Vona B, Esen FN, Sonmez FM, Smol T, Tümer S, Mancılar H, Geylan Durgun DE, Boute O, Moghbeli M, Ghayoor Karimiani E, Hashemi N, Bakhshoodeh B, Kim HG, Maroofian R, Yesilyurt A. Uctepe E, et al. Among authors: kim hg. Eur J Hum Genet. 2024 Jan;32(1):52-60. doi: 10.1038/s41431-023-01461-2. Epub 2023 Oct 26. Eur J Hum Genet. 2024. PMID: 37880421 Free PMC article.
101 results