Samuel S. Chong

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

Terri H. Beaty, Jeffrey C. Murray, Mary L. Marazita et al. · Nature Genetics · 2010 · 583 citations · Full text

Genome-wide Association Study, Allelic Variant, Developmental Biology +9

Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia

Samuel S. Chong, Corinne D. Boehm, Douglas R. Higgs et al. · Blood · 2000 · 468 citations

Cranio-lenticulo-sutural dysplasia is caused by a SEC23A mutation leading to abnormal endoplasmic-reticulum-to-Golgi trafficking

Simeon A. Boyadjiev, J. Christopher Fromme, Jin Ben et al. · Nature Genetics · 2006 · 317 citations

Developmental Anomaly, Developmental Biology, Genetic Disorder +10

Point Mutations and an Intragenic Deletion in LIS1, the Lissencephaly Causative Gene in Isolated Lissencephaly Sequence and Miller-Dieker Syndrome

Cristiana Lo Nigro, Samuel S. Chong, Ann C. M. Smith et al. · Human Molecular Genetics · 1997 · 316 citations · Full text

Distinct haplotype profiles and strong linkage disequilibrium at the MDR1 multidrug transporter gene locus in three ethnic Asian populations

Kun Tang, Soo-Mun Ngoi, Pai-Chung Gwee et al. · Pharmacogenetics · 2002 · 284 citations

Genetics, Genetic Epidemiology, Human Polymorphism +20