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

Year Number of Results
2002 1
2003 3
2005 1
2006 3
2007 1
2008 4
2009 5
2010 4
2011 2
2012 5
2013 2
2014 2
2015 2
2016 2
2017 8
2018 2
2019 13
2020 7
2021 11
2022 7
2023 4
2024 2

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79 results

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Page 1
Development of clinical genetics in Asia.
Chung B, Willis B, Lai PS. Chung B, et al. Among authors: lai ps. Am J Med Genet C Semin Med Genet. 2019 Jun;181(2):150-154. doi: 10.1002/ajmg.c.31700. Epub 2019 Apr 29. Am J Med Genet C Semin Med Genet. 2019. PMID: 31037834
Genetics in Ischemic Stroke: Current Perspectives and Future Directions.
Zhang K, Loong SSE, Yuen LZH, Venketasubramanian N, Chin HL, Lai PS, Tan BYQ. Zhang K, et al. Among authors: lai ps. J Cardiovasc Dev Dis. 2023 Dec 13;10(12):495. doi: 10.3390/jcdd10120495. J Cardiovasc Dev Dis. 2023. PMID: 38132662 Free PMC article. Review.
Training in clinical genetics and genetic counseling in Asia.
Cutiongco-de la Paz EM, Chung BH, Faradz SMH, Thong MK, David-Padilla C, Lai PS, Lin SP, Chen YH, Sura T, Laurino M. Cutiongco-de la Paz EM, et al. Among authors: lai ps. Am J Med Genet C Semin Med Genet. 2019 Jun;181(2):177-186. doi: 10.1002/ajmg.c.31703. Epub 2019 Apr 29. Am J Med Genet C Semin Med Genet. 2019. PMID: 31037827 Review.
Loss of FOCAD, operating via the SKI messenger RNA surveillance pathway, causes a pediatric syndrome with liver cirrhosis.
Moreno Traspas R, Teoh TS, Wong PM, Maier M, Chia CY, Lay K, Ali NA, Larson A, Al Mutairi F, Al-Sannaa NA, Faqeih EA, Alfadhel M, Cheema HA, Dupont J, Bézieau S, Isidor B, Low DY, Wang Y, Tan G, Lai PS, Piloquet H, Joubert M, Kayserili H, Kripps KA, Nahas SA, Wartchow EP, Warren M, Bhavani GS, Dasouki M, Sandoval R, Carvalho E, Ramos L, Porta G, Wu B, Lashkari HP, AlSaleem B, BaAbbad RM, Abreu Ferrão AN, Karageorgou V, Ordonez-Herrera N, Khan S, Bauer P, Cogne B, Bertoli-Avella AM, Vincent M, Girisha KM, Reversade B. Moreno Traspas R, et al. Among authors: lai ps. Nat Genet. 2022 Aug;54(8):1214-1226. doi: 10.1038/s41588-022-01120-0. Epub 2022 Jul 21. Nat Genet. 2022. PMID: 35864190 Free PMC article.
Novel Autoantibodies in Idiopathic Small Fiber Neuropathy.
Chan ACY, Wong HY, Chong YF, Lai PS, Teoh HL, Ng AYY, Hung JHM, Chan YC, Ng KWP, Vijayan J, Ong JJY, Chandra B, Tan CH, Rutt NH, Tan TM, Ismail NH, Wilder-Smith E, Schwarz H, Choi H, Sharma VK, Mak A. Chan ACY, et al. Among authors: lai ps. Ann Neurol. 2022 Jan;91(1):66-77. doi: 10.1002/ana.26268. Epub 2021 Dec 1. Ann Neurol. 2022. PMID: 34761434 Free PMC article.
Blending oxytocin and dopamine with everyday creativity.
Chong A, Tolomeo S, Xiong Y, Angeles D, Cheung M, Becker B, Lai PS, Lei Z, Malavasi F, Tang Q, Chew SH, Ebstein RP. Chong A, et al. Among authors: lai ps. Sci Rep. 2021 Aug 10;11(1):16185. doi: 10.1038/s41598-021-95724-x. Sci Rep. 2021. PMID: 34376746 Free PMC article.
Spinal muscular atrophy: from gene discovery to clinical trials.
Nurputra DK, Lai PS, Harahap NI, Morikawa S, Yamamoto T, Nishimura N, Kubo Y, Takeuchi A, Saito T, Takeshima Y, Tohyama Y, Tay SK, Low PS, Saito K, Nishio H. Nurputra DK, et al. Among authors: lai ps. Ann Hum Genet. 2013 Sep;77(5):435-63. doi: 10.1111/ahg.12031. Epub 2013 Jul 23. Ann Hum Genet. 2013. PMID: 23879295 Review.
79 results