Wilson H.Y. Lo

2.0k total citations
32 papers, 1.3k citations indexed

About

Wilson H.Y. Lo is a scholar working on Molecular Biology, Clinical Biochemistry and Developmental Biology. According to data from OpenAlex, Wilson H.Y. Lo has authored 32 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 8 papers in Clinical Biochemistry and 5 papers in Developmental Biology. Recurrent topics in Wilson H.Y. Lo's work include Metabolism and Genetic Disorders (8 papers), Congenital limb and hand anomalies (5 papers) and Peroxisome Proliferator-Activated Receptors (3 papers). Wilson H.Y. Lo is often cited by papers focused on Metabolism and Genetic Disorders (8 papers), Congenital limb and hand anomalies (5 papers) and Peroxisome Proliferator-Activated Receptors (3 papers). Wilson H.Y. Lo collaborates with scholars based in China, United States and Netherlands. Wilson H.Y. Lo's co-authors include Yan Shen, Ping Liu, Shan Gao, Jun Zhao, Xiaohai Zhang, Guanyun Wu, Changfu Li, Randy C. Eisensmith, Zhijian Yao and Keming Xu and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Annals of Neurology.

In The Last Decade

Wilson H.Y. Lo

32 papers receiving 1.3k citations

Peers

Countries citing papers authored by Wilson H.Y. Lo

Since Specialization

Citations

This map shows the geographic impact of Wilson H.Y. Lo's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Wilson H.Y. Lo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Wilson H.Y. Lo more than expected).

Fields of papers citing papers by Wilson H.Y. Lo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wilson H.Y. Lo. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Wilson H.Y. Lo. The network helps show where Wilson H.Y. Lo may publish in the future.

Co-authorship network of co-authors of Wilson H.Y. Lo

This figure shows the co-authorship network connecting the top 25 collaborators of Wilson H.Y. Lo. A scholar is included among the top collaborators of Wilson H.Y. Lo based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Wilson H.Y. Lo. Wilson H.Y. Lo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Factors Associated With Decreased Kidney Function in HIV-Infected Adults Enrolled in the MTCT-Plus Initiative in Sub-Saharan Africa 2011 ·JAIDS Journal of Acquired Immune Deficiency Syndromes ·Jennifer Jao, Wilson H.Y. Lo, Patricia Lasso Toro, Christina Wyatt, (unknown), Elaine J. Abrams, Rosalind J. Carter	12
2	Adult Clinical and Immunologic Outcomes of the National Antiretroviral Treatment Program in Rwanda During 2004-2005 2009 ·JAIDS Journal of Acquired Immune Deficiency Syndromes ·David Lowrance, (unknown), (unknown), Felix Ndagije, Wilson H.Y. Lo, Donald R. Hoover, (unknown), Batya Elul, (unknown), Tedd V. Ellerbrock, Alphonse Rukundo, Fabienne Shumbusho, Denis Nash, Jules Mugabo, (unknown)	56
3	A novel single-base deletion in ROR2 causes atypical brachydactyly type B1 with cutaneous syndactyly in a large Chinese family 2009 ·Journal of Human Genetics ·Dan Lv, Yang Luo, Wei Yang, Lihua Cao, Yaran Wen, Xiuli Zhao, Miao Sun, Wilson H.Y. Lo, Xue Zhang	9
4	Triphalangeal thumb–polysyndactyly syndrome and syndactyly type IV are caused by genomic duplications involving the long range, limb-specific SHH enhancer 2008 ·Journal of Medical Genetics ·Miao Sun, Fengxia Ma, Xuan Zeng, (unknown), (unknown), (unknown), Guoping Wu, Zuo‐Feng Zhang, B-W Gu, (unknown), (unknown), Binshan Lin, (unknown), XL Zhang, (unknown), Wei Yang, Wilson H.Y. Lo, (unknown), (unknown)	92
5	Three novel mutations of the EDA gene in Chinese patients with X-linked hypohidrotic ectodermal dysplasia 2008 ·British Journal of Dermatology ·Jialiang Zhao, Rui‐Xi Hua, Xiuli Zhao, (unknown), (unknown), Qingyi Liu, (unknown), Mu Sun, Wilson H.Y. Lo, Xuan Zhang	8
6	Novel point mutations in GDF5 associated with two distinct limb malformations in Chinese: brachydactyly type C and proximal symphalangism 2008 ·Journal of Human Genetics ·Wei Yang, Lihua Cao, Wenli Liu, Li Jiang, Miao Sun, Dai Zhang, Shusen Wang, Wilson H.Y. Lo, Yang Luo, Xue Zhang	40
7	Two novel mutations and evidence for haploinsufficiency of the ADAR gene in dyschromatosis symmetrica hereditaria 2006 ·British Journal of Dermatology ·(unknown), Luo Jiang, (unknown), (unknown), (unknown), Miao Sun, Yang Luo, Yong Song, Wilson H.Y. Lo, Xinan Zhang	44
8	A novel deletion in TNNI2 causes distal arthrogryposis in a large Chinese family with marked variability of expression 2006 ·Human Genetics ·Miao Jiang, Xiuli Zhao, (unknown), (unknown), Xuefu Li, (unknown), (unknown), Yun-Qing Li, (unknown), (unknown), Wilson H.Y. Lo, Xue Zhang, Jianxin Li	26
9	Novel Mutations of the RNA-Specific Adenosine Deaminase Gene (DSRAD) in Chinese Families with Dyschromatosis Symmetrica Hereditaria 2004 ·Journal of Investigative Dermatology ·Qing Liu, Wenli Liu, Li Jiang, Miao Sun, (unknown), Xiuli Zhao, Yong Song, Yang Luo, Wilson H.Y. Lo, Xue Zhang	29
10	Association between genetic variation of CACNA1H and childhood absence epilepsy 2003 ·Annals of Neurology ·Yucai Chen, Jianjun Lu, Hong Pan, Yuehua Zhang, Husheng Wu, Keming Xu, Xiaoyan Liu, Yuwu Jiang, Xinhua Bao, Zhijian Yao, Keyue Ding, Wilson H.Y. Lo, Boqin Qiang, Piu Chan, Yan Shen, Xiru Wu	277
11	Postaxial polydactyly type A/B (PAP-A/B) is linked to chromosome 19p13.1-13.2 in a chinese kindred 2002 ·European Journal of Human Genetics ·Hongshan Zhao, Yong Tian, Guido J. Breedveld, Shangzhi Huang, Ying Zou, (unknown), Jinghua Chai, Hui Li, Mingyue Li, Ben A. Oostra, Wilson H.Y. Lo, Peter Heutink	31
12	Characterization of ZNF333, a novel double KRAB domain containing zinc finger gene on human chromosome 19p13.1 2002 ·Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression ·Yong Tian, Guido J. Breedveld, (unknown), Ben A. Oostra, Peter Heutink, Wilson H.Y. Lo	7
13	DSPP mutation in dentinogenesis imperfecta Shields type II 2001 ·Nature Genetics ·Xiaohai Zhang, Jun Zhao, Changfu Li, Shan Gao, (unknown), Ping Liu, Guanyun Wu, (unknown), Wilson H.Y. Lo, Yan Shen	313
14	Another pedigree with pure autosomal dominant spastic paraplegia (AD-FSP) from Tibet mapping to 14q11.2-q24.3 1997 ·Human Genetics ·Shangzhi Huang, Huijun Li, Wilson H.Y. Lo, Christine Fischer, F. Vogel, (unknown), (unknown), (unknown)	15
15	Phenylketonuria in China: Identification and characterization of three novel nucleotide substitutions in the human phenylalanine hydroxylase gene 1994 ·Human Mutation ·Jia Li, Randy C. Eisensmith, Tao Wang, Wilson H.Y. Lo, Shuzhen Huang, Yi‐Tao Zeng, Lifang Yuan, (unknown), Savio L.C. Woo	2
16	Identification of three novel PKU mutations among Chinese: Evidence for recombination or recurrent mutation at the PAH locus 1992 ·Genomics ·Tao Wang, Yoshiyuki Okano, Randy C. Eisensmith, Wilson H.Y. Lo, Shuzhen Huang, Yi‐Tao Zeng, Lifang Yuan, (unknown), Savio L.C. Woo	17
17	Identification of three novel missense PKU mutations among Chinese 1992 ·Genomics ·Jia Li, Randy C. Eisensmith, Tao Wang, Wilson H.Y. Lo, Shuzhen Huang, Yi‐Tao Zeng, Lifang Yuan, (unknown), Savio L.C. Woo	11
18	Missense mutations prevalent in orientals with phenylketonuria: Molecular characterization and clinical implications 1991 ·Genomics ·Tao Wang, Yoshiyuki Okano, Randy C. Eisensmith, Wilson H.Y. Lo, Shu‐Zhen Huang, Yi‐Tao Zeng, Lifang Yuan, (unknown), Savio L.C. Woo	45
19	β-Thalassemia in China: a Systematic Molecular Characterization of β-Thalassemia Mutations 1988 ·Hemoglobin ·Steve S. Huang, Pamela Waber, Carol E. Dowling, Sze Chuen Cesar Wong, Stylianos E. Antonarakis, Ren Cai, Miao Wang, Wilson H.Y. Lo, H H Kazazian	5
20	Cloning and Sequencing of a β-Thalassemia Gene from South China 1988 ·Hemoglobin ·Tao Wang, (unknown), Shangzhi Huang, (unknown), Ren Cai, (unknown), (unknown), Wilson H.Y. Lo	1

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