Ethical considerations of preconception and prenatal gene modification in the embryo and fetus von Mattar, Citra Nurfarah Zaini, Labude, Markus Klaus, Lee, Timothy Nicholas, Lai, Poh San

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A clinical approach to diagnosis and management of mitochondrial myopathies von Chin, Hui-Lin, Lai, Poh San, Tay, Stacey Kiat Hong

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Embryo and fetal gene editing: Technical challenges and progress toward clinical applications von Mattar, Citra N.Z., Chew, Wei Leong, Lai, Poh San

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J’Accuse….. Or The Plight of pro-bono Volunteer Scientists in Academic Publishing von Reichardt, Juergen K. V., Patrinos, George P., Lai, Poh San, Novelli, Giuseppe

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Specific phenotype semantics facilitate gene prioritization in clinical exome sequencing von Tomar, Swati, Sethi, Raman, Lai, Poh San

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Genetic variation in CD38 and breastfeeding experience interact to impact infants’ attention to social eye cues von Krol, Kathleen M., Monakhov, Mikhail, San Lai, Poh, Ebstein, Richard P., Grossmann, Tobias

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Novel Autoantibodies in Idiopathic Small Fiber Neuropathy von Chan, Amanda C. Y., Wong, Hiu Yi, Chong, Yao Feng, Lai, Poh San, Teoh, Hock Luen, Ng, Alison Y. Y., Hung, Jennifer H. M., Chan, Yee Cheun, Ng, Kay W. P., Vijayan, Joy, Ong, Jonathan J. Y., Chandra, Bharatendu, Tan, Chi Hsien, Rutt, Nurul H., Tan, Ti Myen, Ismail, Nur Hafiza, Wilder‐Smith, Einar, Schwarz, Herbert, Choi, Hyungwon, Sharma, Vijay K., Mak, Anselm

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Blending oxytocin and dopamine with everyday creativity von Chong, Anne, Tolomeo, Serenella, Xiong, Yue, Angeles, Dario, Cheung, Mike, Becker, Benjamin, Lai, Poh San, Lei, Zhen, Malavasi, Fabio, Tang, Qianzi, Chew, Soo Hong, Ebstein, Richard P.

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High incidence of allelic loss at 16q12.2 region spanning RBL2/p130 gene in retinoblastoma von Priya, Kadam, Jada, Srinivasa Rao, Quah, Boon Long, Quah, Thuan Chong, Lai, Poh San

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Autosomal dominant Emery-Dreifuss muscular dystrophy caused by a mutation in the lamin A/C gene identified by exome sequencing: a case report von Iskandar, Kristy, Astari, Farida Niken, Gumilang, Rizki Amalia, Ilma, Nissya, Shartyanie, Ni Putu, Adistyawan, Guritno, Tan, Grace, Lai, Poh San

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Delay discounting, genetic sensitivity, and leukocyte telomere length von Yim, Onn-Siong, Zhang, Xing, Shalev, Idan, Monakhov, Mikhail, Zhong, Songfa, Hsu, Ming, Chew, Soo Hong, San Lai, Poh, Ebstein, Richard P.

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Ethics and regulatory considerations for the clinical translation of somatic cell human epigenetic editing von Zeps, Nikolajs, Lysaght, Tamra, Chadwick, Ruth, Erler, Alexandre, Foo, Roger, Giordano, Simona, San Lai, Poh, Schaefer, G. Owen, Xafis, Vicki, Chew, Wei Leong, Sugarman, Jeremy

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Intragenic mutations in SMN1 may contribute more significantly to clinical severity than SMN2 copy numbers in some spinal muscular atrophy (SMA) patients von Yamamoto, Tomoto, Sato, Hideyuki, Lai, Poh San, Nurputra, Dian Kesumapramudya, Harahap, Nur Imma Fatimah, Morikawa, Satoru, Nishimura, Noriyuki, Kurashige, Takashi, Ohshita, Tomohiko, Nakajima, Hideki, Yamada, Hiroyuki, Nishida, Yoshinobu, Toda, Soichiro, Takanashi, Jun-ichi, Takeuchi, Atsuko, Tohyama, Yumi, Kubo, Yuji, Saito, Kayoko, Takeshima, Yasuhiro, Matsuo, Masafumi, Nishio, Hisahide

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Intron-retained transcripts of the spinal muscular atrophy genes, SMN1 and SMN2 von Harahap, Nur Imma Fatimah, Niba, Emma Tabe Eko, Ar Rochmah, Mawaddah, Wijaya, Yogik Onky Silvana, Saito, Toshio, Saito, Kayoko, Awano, Hiroyuki, Morioka, Ichiro, Iijima, Kazumoto, Lai, Poh San, Matsuo, Masafumi, Nishio, Hisahide, Shinohara, Masakazu

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Effect of semaphorin 3C gene variants in multifactorial Hirschsprung disease von Gunadi, Ryantono, Fiko, Sethi, Raman, Marcellus, Kalim, Alvin Santoso, Imelda, Priscillia, Melati, Devy, Simanjaya, Susan, Widitjiarso, William, Pitaka, Ririd Tri, Arfian, Nur, Iskandar, Kristy, Makhmudi, Akhmad, Lai, Poh San

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SMA mutations in SMN Tudor and C-terminal domains destabilize the protein von Takarada, Toru, Ar Rochmah, Mawaddah, Harahap, Nur Imma Fatimah, Shinohara, Masakazu, Saito, Toshio, Saito, Kayoko, Lai, Poh San, Bouike, Yoshihiro, Takeshima, Yasuhiro, Awano, Hiroyuki, Morioka, Ichiro, Iijima, Kazumoto, Nishio, Hisahide, Takeuchi, Atsuko

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A novel transthyretin mutation V32A in a Chinese man with late-onset amyloid polyneuropathy von Pica, Emmanuel C., Pramono, Zacharias Ad, Verma, Kamal K., San, Lai Poh, Chee, Yee Woon

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Molecular diagnosis of neurogenetic disorders involving trinucleotide repeat expansions von Tan, Ene-Choo, Lai, Poh San

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The contributions of oxytocin and vasopressin pathway genes to human behavior von Ebstein, Richard P., Knafo, Ariel, Mankuta, David, Chew, Soo Hong, Lai, Poh San

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Association among dispositional mindfulness, self-compassion, and leukocyte telomere length in Chinese adults von Keng, Shian-Ling, Yim, Onn Siong, Lai, Poh San, Chew, Soo Hong, Ebstein, Richard P

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