Contribution of Four Polymorphisms in Renin-Angiotensin-Aldosterone-Related Genes to Hypertension in a Thai Population by Pimphen Charoen, Jakris Eu-ahsunthornwattana, Nisakron Thongmung, Pedro A. Jose, Piyamitr Sritara, Prin Vathesatogkit, Chagriya Kitiyakara

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Comparison of methods to account for relatedness in genome-wide association studies with family-based data. by Jakris Eu-Ahsunthornwattana, E Nancy Miller, Michaela Fakiola, Wellcome Trust Case Control Consortium 2, Selma M B Jeronimo, Jenefer M Blackwell, Heather J Cordell

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PROC Promoter Single Nucleotide Polymorphisms Associated With Low Protein C Activity But Not Increased Risk of Thromboembolism in Pediatric Population by Natsumon Udomkittivorakul MD, Werasak Sasanakul BSc, Jakris Eu-ahsunthornwattana MD, PhD, Ampaiwan Chuansumrit MD, Patcharee Komwilaisak MD, Duantida Songdej MD, PhD, Nongnuch Sirachainan MD

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A comprehensive Thai pharmacogenomics database (TPGxD‐1): Phenotype prediction and variants identification in 942 whole‐genome sequencing data by Shobana John, Sommon Klumsathian, Paravee Own‐eium, Jakris Eu‐ahsunthornwattana, Thanyachai Sura, Donniphat Dejsuphong, Piyamitr Sritara, Prin Vathesatogkit, Nartthawee Thongchompoo, Wiphaporn Thabthimthong, Nuttinee Teerakulkittipong, Wasun Chantratita, Chonlaphat Sukasem

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Thai pharmacogenomics database −2 (TPGxD‐2) sequel to TPGxD‐1, analyzing genetic variants in 26 non‐VIPGx genes within the Thai population by Shobana John, Sommon Klumsathian, Paravee Own‐eium, Angkana Charoenyingwattana, Jakris Eu‐ahsunthornwattana, Thanyachai Sura, Donniphat Dejsuphong, Piyamitr Sritara, Prin Vathesatogkit, Nartthawee Thongchompoo, Wiphaporn Thabthimthong, Nuttinee Teerakulkittipong, Wasun Chantratita, Chonlaphat Sukasem

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Association of genetic variation on X chromosome with systemic lupus erythematosus in both Thai and Chinese populations by Yi Yang, Prapaporn Pisitkun, Wanling Yang, Natini Jinawath, Yao Lei, Yong-Fei Wang, Nattiya Hirankarn, Surakameth Mahasirimongkol, Wichai Aekplakorn, Pattarin Tangtanatakul, Krisana Jaiwan, Manon Boonbangyang, Punna Kunhapan, Pimpayao Sodsai, Jakris Eu-Ahsunthornwattana, Nareemarn Neelapaichit

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Infantile onset Sandhoff disease: clinical manifestation and a novel common mutation in Thai patients by Thipwimol Tim-Aroon, Khunton Wichajarn, Kamornwan Katanyuwong, Pranoot Tanpaiboon, Nithiwat Vatanavicharn, Kullasate Sakpichaisakul, Arthaporn Kongkrapan, Jakris Eu-ahsunthornwattana, Supranee Thongpradit, Kanya Moolsuwan, Nusara Satproedprai, Surakameth Mahasirimongkol, Tassanee Lerksuthirat, Bhoom Suktitipat, Natini Jinawath, Duangrurdee Wattanasirichaigoon

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