| # | Title | Journal | Year | Citations |
|---|
| 1 | Test for Escherichia coli Enterotoxin Using Infant Mice: Application in a Study of Diarrhea in Children in Honolulu | Journal of Infectious Diseases | 1972 | 1,131 |
| 2 | Prenatal methylmercury exposure from ocean fish consumption in the Seychelles child development study | Lancet, The | 2003 | 534 |
| 3 | A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13 | Human Molecular Genetics | 2016 | 163 |
| 4 | Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate | Human Genetics | 2017 | 139 |
| 5 | Newborn screening in the Asia Pacific region | Journal of Inherited Metabolic Disease | 2007 | 116 |
| 6 | Outcome of the vaginal infections and prematurity study: Results of a clinical trial of erythromycin among pregnant women colonized with group B streptococci | American Journal of Obstetrics and Gynecology | 1995 | 96 |
| 7 | Developmental changes in the myocardial architecture of the chick | The Anatomical Record | 1997 | 96 |
| 8 | An assessment of hepatitis E virus (HEV) in US blood donors and recipients: no detectable HEV RNA in 1939 donors tested and no evidence for HEV transmission to 362 prospectively followed recipients | Transfusion | 2013 | 95 |
| 9 | Adrenoleukodystrophy: Dietary oleic acid lowers hexacosanoate levels | Annals of Neurology | 1987 | 94 |
| 10 | Hemorrhagic Disease in an Infant Due to Deficiency of a Previously Undescribed Clotting Factor | Blood | 1952 | 88 |
| 11 | Associations between uncoupling protein 2, body composition, and resting energy expenditure in lean and obese African American, white, and Asian children | American Journal of Clinical Nutrition | 2000 | 88 |
| 12 | AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME | Pediatric Clinics of North America | 2000 | 88 |
| 13 | Opitz G/BBB Syndrome in Xp22: Mutations in the MID1 Gene Cluster in the Carboxy-Terminal Domain | American Journal of Human Genetics | 1998 | 63 |
| 14 | Pathogenic mutations inGLI2cause a specific phenotype that is distinct from holoprosencephaly | Journal of Medical Genetics | 2014 | 53 |
| 15 | Studies of the development of congenital anomalies in embryos of riboflavin-deficient, galactoflavin fed rats. II. Role of the terminal electron transport systems | Teratology | 1968 | 51 |
| 16 | Analysis of renal anomalies in VACTERL association | Birth Defects Research Part A: Clinical and Molecular Teratology | 2014 | 38 |
| 17 | Association studies of low‐frequency coding variants in nonsyndromic cleft lip with or without cleft palate | American Journal of Medical Genetics, Part A | 2017 | 36 |
| 18 | A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals | Genetic Epidemiology | 2019 | 36 |
| 19 | Analysis of cardiac anomalies in VACTERL association | Birth Defects Research Part A: Clinical and Molecular Teratology | 2013 | 28 |
| 20 | Molecular Size Studies on 6-Phosphogluconate Dehydrogenase | Nature | 1966 | 27 |
| 21 | Anxiety symptoms and children's eye gaze during fear learning | Journal of Child Psychology and Psychiatry and Allied Disciplines | 2017 | 26 |
| 22 | Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes | Genetic Epidemiology | 2017 | 24 |
| 23 | Mutations of the CYP21 Gene in Nonclassical Steroid 21-Hydroxylase Deficiency in Japan. | Endocrine Journal | 1998 | 21 |
| 24 | Glucose and Free Fatty Acid Metabolism in Obese Adolescents | American Journal of Clinical Nutrition | 1965 | 18 |
| 25 | Association of low‐frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts | American Journal of Medical Genetics, Part A | 2019 | 18 |
| 26 | Parental attitudes regarding interviews about injuries to their children | Injury Prevention | 2000 | 16 |
| 27 | Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions | Frontiers in Cell and Developmental Biology | 2021 | 16 |
| 28 | An Evaluation of the Single‐Channel Auto Analyzer in the Quantitation of Anti‐Rh0 | Vox Sanguinis | 1970 | 14 |
| 29 | The Blood Group Antibody Anti-s A Third Example | Vox Sanguinis | 1957 | 8 |
| 30 | GWAS reveals loci associated with velopharyngeal dysfunction | Scientific Reports | 2018 | 8 |
| 31 | Malabsorption and protein-losing enteropathy in a child with X-linked agammaglobulinemia | Clinical Immunology and Immunopathology | 1975 | 5 |
| 32 | Prevalence of Torus Palatinus and association with dental arch shape in a multi-ethnic cohort | HOMO- Journal of Comparative Human Biology | 2020 | 5 |
| 33 | Energy-dependent expression of platelet-von Willebrand factor on the surface of unstimulated and stimulated platelets | Translational Research | 1997 | 4 |
| 34 | Parents of Children With Nonsyndromic Orofacial Clefting Show Altered Palate Shape | Cleft Palate-Craniofacial Journal | 2021 | 4 |
| 35 | Genome‐wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes | Genetic Epidemiology | 2022 | 4 |
| 36 | LIPID COMPOSITION AND SYNTHESIS OF ISOLATED LYMPHOCYTES FROM PATIENTS WITH DOWN'S SYNDROME* | Journal of Intellectual Disability Research | 1969 | 1 |
| 37 | 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 | 2019 | 1 |
| 38 | The Influence of Sex and Ancestry on Three-Dimensional Palate Shape | Journal of Craniofacial Surgery | 2021 | 1 |
