Jacques Zaneveld - Concepedia

Concepedia

Author

Jacques Zaneveld

Baylor College of Medicine

Also Known As

J. E. Zaneveld, J. Eric Zaneveld, J.E. Zaneveld, Jacques E Zaneveld, Jacques E. Zaneveld, Jacques Eric Zaneveld, Jacques Zaneveld

16

Publications

1.4K

Citations

11

H-Index

31

Concepts

All Affiliations

Baylor College of Medicine Baylor Genetics Peking Union Medical College Hospital Chinese Academy of Medical Sciences & Peking Union Medical College McGill University Health Centre

JZ

About

Jacques Zaneveld is an author at Baylor College of Medicine specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	386
2	Health Sciences	1	1	11
3	Natural Sciences	1	1	93
4	Cell Biology	1	1	11
5	Molecular Biology	1	1	93

Jacques Zaneveld

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11

Publications

1.4K

Citations

11

H-Index

	Year	Citations
TET2 mutations predict response to hypomethylating agents in myelodysplastic syndrome patients Rafael Bejar, Allegra M. Lord, Kristen E. Stevenson, Blood	2014	543
Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements Feng Wang, Hui Wang, Han-Fang Tuan, Human Genetics Molecular Diagnostic TechniquesRetinitis PigmentosaGeneticsMedicineNext-generation Sequencing	2013	235
Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencing Xia Wang, Hui Wang, Vincent Sun, Journal of Medical Genetics	2013	160
Next-Generation Sequencing–Based Molecular Diagnosis of a Chinese Patient Cohort With Autosomal Recessive Retinitis Pigmentosa Qing Fu, Feng Wang, Hui Wang, Investigative Ophthalmology & Visual Science	2013	99
Next-generation sequencing-based molecular diagnosis of 82 retinitis pigmentosa probands from Northern Ireland Li Zhao, Feng Wang, Hui Wang, Human Genetics BioinformaticsDna SequencingRetinitis PigmentosaMedicineNatural Sciences	2014	93
Genome-wide association scan in north Indians reveals three novel HLA-independent risk loci for ulcerative colitis Garima Juyal, Sapna Negi, Ajit Sood, Gut	2014	66
Comprehensive molecular diagnosis of 67 Chinese Usher syndrome probands: high rate of ethnicity specific mutations in Chinese USH patients Lichun Jiang, Xiaofang Liang, Yumei Li, Orphanet Journal of Rare Diseases	2015	54
Comprehensive analysis of patients with Stargardt macular dystrophy reveals new genotype–phenotype correlations and unexpected diagnostic revisions Jacques Zaneveld, Sorath Noorani Siddiqui, Huajin Li, Genetics in Medicine Ocular DiseaseOphthalmologyGeneticsGenetic EpidemiologyUnexpected Diagnostic Revisions	2014	47
A Homozygous Missense Mutation in NEUROD1 Is Associated With Nonsyndromic Autosomal Recessive Retinitis Pigmentosa H. Li, Min Xu, H. Li, Investigative Ophthalmology & Visual Science	2014	27
Ku DNA End-Binding Activity Promotes Repair Fidelity and Influences End-Processing During Nonhomologous End-Joining in <i>Saccharomyces cerevisiae</i> Charlene H. Emerson, Christopher R. Lopez, Albert Ribes‐Zamora, Genetics	2018	17

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