Poh-San Lai (P S Lai, Poh San Lai)

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 18

Top Topics

Advance Care Planning

Top Venues

American journal of medical genetics. Part C, Seminars in medical genetics

Annals of neurology

BMC medical genomics

This page only lists publications with an associated author ORCID identifier.

Publications

Ery Kus Dwianingsih, Kristy Iskandar, Sunartini Hapsara, Chun Ping Liu, Rusdy Ghazali Malueka, null Gunadi, Masafumi Matsuo, Poh-San Lai
Mutation spectrum analysis of DMD gene in Indonesian Duchenne and Becker muscular dystrophy patients. F1000Research 11 (2023)
Amanda C Y Chan, Shivaram Kumar, Grace Tan, Anna Hiu Yi Wong, Jonathan Jia Yuan Ong, Bharatendu Chandra, Hua Huang, Vijay Kumar Sharma, Poh-San Lai
Expanding the genetic causes of small-fiber neuropathy: SCN genes and beyond. Muscle & nerve (2022)
Citra Nurfarah Zaini Mattar, Markus Klaus Labude, Timothy Nicholas Lee, Poh-San Lai
Ethical considerations of preconception and prenatal gene modification in the embryo and fetus. Human reproduction (Oxford, England) 36 (12) (2022)
Markus K Labude, Vicki Xafis, Poh-San Lai, Catherine Mills
Vulnerability and the Ethics of Human Germline Genome Editing. The CRISPR journal 5 (3) (2022)
Dineshani Hettiarachchi, S M V Subasinghe, G G Anandagoda, Hetalkumar Panchal, Poh-San Lai, Vajira H W Dissanayake
Novel frameshift variant in the PCNT gene associated with Microcephalic Osteodysplastic Primordial Dwarfism (MOPD) Type II and small kidneys. BMC medical genomics 15 (1) (2022)
Vicki Xafis, Gerald Owen Schaefer, Markus K Labude, Yujia Zhu, Soren Holm, Roger Sik Yin Foo, Poh-San Lai, Ruth Chadwick
Germline genome modification through novel political, ethical, and social lenses. PLoS genetics 17 (9) (2021)
Amanda C Y Chan, Hiu Yi Wong, Yao Feng Chong, Poh-San Lai, Hock Luen Teoh, Alison Y Y Ng, Jennifer H M Hung, Yee Cheun Chan, Kay W P Ng, Joy Vijayan, Jonathan J Y Ong, Bharatendu Chandra, Chi Hsien Tan, Nurul H Rutt, Ti Myen Tan, Nur Hafiza Ismail, Einar Wilder-Smith, Herbert Schwarz, Hyungwon Choi, Vijay K Sharma, Anselm Mak
Novel Autoantibodies in Idiopathic Small Fiber Neuropathy. Annals of neurology (2021)
. Gunadi, Fiko Ryantono, Raman Sethi, null Marcellus, Alvin Santoso Kalim, Priscillia Imelda, Devy Melati, Susan Simanjaya, William Widitjiarso, Ririd Tri Pitaka, Nur Arfian, Kristy Iskandar, Akhmad Makhmudi, Poh-San Lai
Effect of semaphorin 3C gene variants in multifactorial Hirschsprung disease. The Journal of international medical research 49 (2) (2021)
Yan Shan Ang, Poh-San Lai, Lin-Yue Lanry Yung
Design of Split Proximity Circuit as a Plug-and-Play Translator for Point Mutation Discrimination. Analytical chemistry 92 (16) (2020)
Neha S Bhatia, Jiin Ying Lim, Carine Bonnard, Jyn-Ling Kuan, Maggie Brett, Heming Wei, Breana Cham, Huilin Chin, Celia Bosso-Lefevre, Perumal Dharuman, Nathalie Escande-Beillard, Arun George Devasia, Chew Yin Jasmine Goh, Sylvia Kam, Wendy Kein-Meng Liew, Woei Kang Liew, Grace Lin, Kanika Jain, Alvin Yu-Jin Ng, Deepa Subramanian, Min Xie, Yuen-Ming Tan, Nilesh R Tawari, Zenia Tiang, Teck Wah Ting, Sumanty Tohari, Cheuk Ka Tong, Alexander Lezhava, Sarah B Ng, Hai Yang Law, Byrappa Venkatesh, Swati Tomar, Raman Sethi, Grace Tan, Arthi Shanmugasundaram, Denise Li-Meng Goh, Poh-San Lai, Angeline Lai, Ee Shien Tan, Ivy Ng, Bruno Reversades, Ene Choo Tan, Roger Foo, Saumya Shekhar Jamuar, null null
Singapore Undiagnosed Disease Program: Genomic Analysis aids Diagnosis and Clinical Management. Archives of disease in childhood 106 (1) (2020)
Dineshani Hettiarachchi, Hetalkumar Panchal, B A P S Pathirana, P D Rathnayaka, A Padeniya, Poh-San Lai, Vajira H W Dissanayake
Six Novel ATM Gene Variants in Sri Lankan Patients with Ataxia Telangiectasia. Case reports in genetics 2020 (2020)
Kuen Kuen Lam, Raman Sethi, Grace Tan, Swati Tomar, Michelle Lo, Carol Loi, Choong Leong Tang, Emile Tan, Poh-San Lai, Peh Yean Cheah
The orphan nuclear receptor NR0B2 could be a novel susceptibility locus associated with microsatellite-stable, APC mutation-negative early-onset colorectal carcinomas with metabolic manifestation. Genes, chromosomes & cancer 60 (2) (2020)
Dineshani Hettiarachchi, Hetalkumar Panchal, Poh-San Lai, V H W Dissanayake
Novel variant in NSDHL gene associated with CHILD syndrome and syndactyly- a case report. BMC medical genetics 21 (1) (2020)
Pornswan Wasant, Carmencita Padilla, Stephen Lam, Meow-Keong Thong, Poh-San Lai
Asia Pacific Society of Human Genetics (APSHG) from conception to 2019: 13 years of collaboration to tackle congenital malformation and genetic disorders in Asia. American journal of medical genetics. Part C, Seminars in medical genetics 181 (2) (2019)
Brian Hon-Yin Chung, Brooke Willis, Poh-San Lai
Development of clinical genetics in Asia. American journal of medical genetics. Part C, Seminars in medical genetics 181 (2) (2019)
Swati Tomar, Vikaesh Moorthy, Raman Sethi, Josiah Chai, Poh Sim Low, Stacey Tay Kiat Hong, Poh-San Lai
Mutational spectrum of dystrophinopathies in Singapore: Insights for genetic diagnosis and precision therapy. American journal of medical genetics. Part C, Seminars in medical genetics 181 (2) (2019)
Eva Maria Cutiongco-de la Paz, Brian Hon-Yin Chung, Sultana M H Faradz, Meow-Keong Thong, Carmencita David-Padilla, Poh-San Lai, Shuan-Pei Lin, Yin-Hsiu Chen, Thanyachai Sura, Mercy Laurino
Training in clinical genetics and genetic counseling in Asia. American journal of medical genetics. Part C, Seminars in medical genetics 181 (2) (2019)
Swati Tomar, Raman Sethi, Poh-San Lai
Specific phenotype semantics facilitate gene prioritization in clinical exome sequencing. European journal of human genetics : EJHG 27 (9) (2019)