Samuel S. Chong - Concepedia

Author

Samuel S. Chong

Also Known As

Chong, Samuel S., Chong, Samuel Siong Chuan, Chuanhui Xu, S CHONG, S Chong, S S Chong, S. CHONG, S. Chong, S. S. C. Chong, S. S. Chong

225

Publications

7.7K

Citations

H-Index

151

Concepts

All Affiliations

National University of Singapore National University Hospital Johns Hopkins University Johns Hopkins Medicine KK Women's and Children's Hospital

About

Samuel S. Chong is an author at National University of Singapore specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	26	44	3.2K
2	Public Health	9	9	810
3	Natural Sciences	8	8	195
4	Social Sciences	2	2	243
5	Engineering	1	1	13

Samuel S. Chong

110

Publications

6.4K

Citations

H-Index

Page 1

	Year	Citations
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, Nature Genetics Genome-wide Association StudyAllelic VariantDevelopmental BiologyGeneticsCleft Palate Identifies	2010	583
Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia Samuel S. Chong, Corinne D. Boehm, Douglas R. Higgs, Blood	2000	468
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, Nature Genetics Developmental AnomalyDevelopmental BiologyGenetic DisorderPathologyCraniofacial Development	2006	317
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, Human Molecular Genetics	1997	316
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, Pharmacogenetics GeneticsGenetic EpidemiologyHuman PolymorphismPathologyStrong Linkage Disequilibrium	2002	284
A Revision of the Lissencephaly and Miller-Dieker Syndrome Critical Regions in Chromosome 17p13.3 Samuel S. Chong, Svetlana Pack, Anna V. Roschke, Human Molecular Genetics	1997	191
Gametic and somatic tissue–specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1 Samuel S. Chong, Alanna E. McCall, Juan Cota, Nature Genetics Sca1 Cag RepeatMolecular NeuroscienceSynaptic SignalingNeuroanatomySomatic Tissue–specific Heterogeneity	1995	190
Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate Terri H. Beaty, Ingo Ruczinski, Jeffrey C. Murray, Genetic Epidemiology Multiple SnpsGeneticsGenetic EpidemiologyCp CaseNonsyndromic Cleft Palate	2011	188
Circulating microRNAs as Potential Diagnostic and Prognostic Biomarkers in Hepatocellular Carcinoma Jin Yu, Ye Shen Wong, Brian K. P. Goh, Scientific Reports	2019	140
Association between IRF6 and nonsyndromic cleft lip with or without cleft palate in four populations Ji Wan Park, Iain McIntosh, Jacqueline B. Hetmanski, Genetics in Medicine Developmental BiologyNonsyndromic Cleft LipGeneticsPathologyCraniofacial Anomalies	2007	124

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