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

Year Number of Results
1963 2
1964 1
1966 1
1967 1
1969 1
1970 1
1973 2
1978 1
1979 3
1981 4
1982 1
1983 2
1984 1
1985 1
1986 2
1987 1
1988 2
1989 3
1990 4
1991 4
1992 8
1993 3
1994 2
1995 3
1996 4
1997 1
1999 1
2000 1
2001 1
2002 1
2003 2
2004 3
2005 7
2006 8
2007 7
2008 13
2009 10
2010 8
2011 5
2012 6
2013 6
2014 12
2015 18
2016 18
2017 12
2018 17
2019 18
2020 18
2021 18
2022 32
2023 19
2024 9

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287 results

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Page 1
Analysis of clinically relevant variants from ancestrally diverse Asian genomes.
Chan SH, Bylstra Y, Teo JX, Kuan JL, Bertin N, Gonzalez-Porta M, Hebrard M, Tirado-Magallanes R, Tan JHJ, Jeyakani J, Li Z, Chai JF, Chong YS, Davila S, Goh LL, Lee ES, Wong E, Wong TY; SG10K_Health Consortium; Prabhakar S, Liu J, Cheng CY, Eisenhaber B, Karnani N, Leong KP, Sim X, Yeo KK, Chambers JC, Tai ES, Tan P, Jamuar SS, Ngeow J, Lim WK. Chan SH, et al. Nat Commun. 2022 Nov 5;13(1):6694. doi: 10.1038/s41467-022-34116-9. Nat Commun. 2022. PMID: 36335097 Free PMC article.
Nanoparticles' interactions with vasculature in diseases.
Tee JK , Yip LX , Tan ES , Santitewagun S , Prasath A , Ke PC , Ho HK , Leong DT . Tee JK , et al. Among authors: tan es. Chem Soc Rev. 2019 Oct 28;48(21):5381-5407. doi: 10.1039/c9cs00309f. Chem Soc Rev. 2019. PMID: 31495856 Review.
The diabetes-atrial fibrillation paradox.
Tan ESJ, Tay WT, Teng TK, Richards AM, Doughty RN, Lam CSP. Tan ESJ, et al. Heart. 2019 Jun;105(11):893. doi: 10.1136/heartjnl-2019-315018. Heart. 2019. PMID: 31092681 No abstract available.
Nail psoriasis: a review.
Tan ES, Chong WS, Tey HL. Tan ES, et al. Am J Clin Dermatol. 2012 Dec 1;13(6):375-88. doi: 10.2165/11597000-000000000-00000. Am J Clin Dermatol. 2012. PMID: 22784035 Review.
Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome.
Cousin MA, Veale EL, Dsouza NR, Tripathi S, Holden RG, Arelin M, Beek G, Bekheirnia MR, Beygo J, Bhambhani V, Bialer M, Bigoni S, Boelman C, Carmichael J, Courtin T, Cogne B, Dabaj I, Doummar D, Fazilleau L, Ferlini A, Gavrilova RH, Graham JM Jr, Haack TB, Juusola J, Kant SG, Kayani S, Keren B, Ketteler P, Klöckner C, Koopmann TT, Kruisselbrink TM, Kuechler A, Lambert L, Latypova X, Lebel RR, Leduc MS, Leonardi E, Lewis AM, Liew W, Machol K, Mardini S, McWalter K, Mignot C, McLaughlin J, Murgia A, Narayanan V, Nava C, Neuser S, Nizon M, Ognibene D, Park J, Platzer K, Poirsier C, Radtke M, Ramsey K, Runke CK, Guillen Sacoto MJ, Scaglia F, Shinawi M, Spranger S, Tan ES, Taylor J, Trentesaux AS, Vairo F, Willaert R, Zadeh N, Urrutia R, Babovic-Vuksanovic D, Zimmermann MT, Mathie A, Klee EW. Cousin MA, et al. Among authors: tan es. Genome Med. 2022 Jun 13;14(1):62. doi: 10.1186/s13073-022-01064-4. Genome Med. 2022. PMID: 35698242 Free PMC article.
Left Ventricular Non-compaction: Is It Genetic?
Ting TW, Jamuar SS, Brett MS, Tan ES, Cham BW, Lim JY, Law HY, Tan EC, Choo JT, Lai AH. Ting TW, et al. Among authors: tan es. Pediatr Cardiol. 2015 Dec;36(8):1565-72. doi: 10.1007/s00246-015-1222-5. Epub 2015 Jun 25. Pediatr Cardiol. 2015. PMID: 26108892 Review.
Inactivation of DRG1, encoding a translation factor GTPase, causes a recessive neurodevelopmental disorder.
Westrip CAE, Paul F, Al-Murshedi F, Qaitoon H, Cham B, Fletcher SC, Hendrix E, Boora U, Ng AYJ, Bonnard C, Najafi M, Alawbathani S, Lambert I, Fox G, Venkatesh B, Bertoli-Avella A, Tan ES, Al-Maawali A, Reversade B, Coleman ML. Westrip CAE, et al. Among authors: tan es. Genet Med. 2023 Sep;25(9):100893. doi: 10.1016/j.gim.2023.100893. Epub 2023 May 11. Genet Med. 2023. PMID: 37179472 Free article.
Does estrogen regulate vitellogenin synthesis in corals?
Tan ES, Hamazato H, Ishii T, Taira K, Takeuchi Y, Takekata H, Isomura N, Takemura A. Tan ES, et al. Comp Biochem Physiol A Mol Integr Physiol. 2021 May;255:110910. doi: 10.1016/j.cbpa.2021.110910. Epub 2021 Jan 22. Comp Biochem Physiol A Mol Integr Physiol. 2021. PMID: 33486078
Williams-Beuren syndrome in diverse populations.
Kruszka P, Porras AR, de Souza DH, Moresco A, Huckstadt V, Gill AD, Boyle AP, Hu T, Addissie YA, Mok GTK, Tekendo-Ngongang C, Fieggen K, Prijoles EJ, Tanpaiboon P, Honey E, Luk HM, Lo IFM, Thong MK, Muthukumarasamy P, Jones KL, Belhassan K, Ouldim K, El Bouchikhi I, Bouguenouch L, Shukla A, Girisha KM, Sirisena ND, Dissanayake VHW, Paththinige CS, Mishra R, Kisling MS, Ferreira CR, de Herreros MB, Lee NC, Jamuar SS, Lai A, Tan ES, Ying Lim J, Wen-Min CB, Gupta N, Lotz-Esquivel S, Badilla-Porras R, Hussen DF, El Ruby MO, Ashaat EA, Patil SJ, Dowsett L, Eaton A, Innes AM, Shotelersuk V, Badoe Ë, Wonkam A, Obregon MG, Chung BHY, Trubnykova M, La Serna J, Gallardo Jugo BE, Chávez Pastor M, Abarca Barriga HH, Megarbane A, Kozel BA, van Haelst MM, Stevenson RE, Summar M, Adeyemo AA, Morris CA, Moretti-Ferreira D, Linguraru MG, Muenke M. Kruszka P, et al. Among authors: tan es. Am J Med Genet A. 2018 May;176(5):1128-1136. doi: 10.1002/ajmg.a.38672. Am J Med Genet A. 2018. PMID: 29681090 Free PMC article.
287 results