Jacques Zaneveld

1.4k total citations · 1 hit paper
13 papers, 749 citations indexed

About

Jacques Zaneveld is a scholar working on Molecular Biology, Ophthalmology and Surgery. According to data from OpenAlex, Jacques Zaneveld has authored 13 papers receiving a total of 749 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 4 papers in Ophthalmology and 2 papers in Surgery. Recurrent topics in Jacques Zaneveld's work include Retinal Development and Disorders (6 papers), Retinal Diseases and Treatments (4 papers) and Acute Myeloid Leukemia Research (2 papers). Jacques Zaneveld is often cited by papers focused on Retinal Development and Disorders (6 papers), Retinal Diseases and Treatments (4 papers) and Acute Myeloid Leukemia Research (2 papers). Jacques Zaneveld collaborates with scholars based in United States, China and Canada. Jacques Zaneveld's co-authors include Michal Bar‐Natan, Bennett Adam Caughey, David P. Steensma, Rafael Bejar, Kristen E. Stevenson, Petar Stojanov, Benjamin L. Ebert, Donna Neuberg, Gad Getz and Allegra M. Lord and has published in prestigious journals such as Blood, PLoS ONE and Gut.

In The Last Decade

Jacques Zaneveld

13 papers receiving 741 citations

Hit Papers

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What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

TET2 mutations predict response to hypomethylating agents in myelodysplastic syndrome patients

2014 405 citations Rafael Bejar, Allegra M. Lord et al. Blood profile →

Peers

Countries citing papers authored by Jacques Zaneveld

Since Specialization

Citations

This map shows the geographic impact of Jacques Zaneveld'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 Jacques Zaneveld with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jacques Zaneveld more than expected).

Fields of papers citing papers by Jacques Zaneveld

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jacques Zaneveld. 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 Jacques Zaneveld. The network helps show where Jacques Zaneveld may publish in the future.

Co-authorship network of co-authors of Jacques Zaneveld

This figure shows the co-authorship network connecting the top 25 collaborators of Jacques Zaneveld. A scholar is included among the top collaborators of Jacques Zaneveld 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 Jacques Zaneveld. Jacques Zaneveld is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

#	Work	Indexed citations
1	Gene Therapy Rescues Retinal Degeneration in Receptor Expression-Enhancing Protein 6 Mutant Mice 2018 ·Human Gene Therapy ·(unknown), Aiden Eblimit, Qingnan Liang, (unknown), (unknown), Hehe Liu, Quynh Nguyen, Jacques Zaneveld, Keqing Wang, Yumei Li, Rui Chen	9
2	Ku DNA End-Binding Activity Promotes Repair Fidelity and Influences End-Processing During Nonhomologous End-Joining in Saccharomyces cerevisiae 2018 ·Genetics ·(unknown), (unknown), Albert Ribes‐Zamora, (unknown), Christopher L. Williams, (unknown), Jacques Zaneveld, Rui Chen, Alison A. Bertuch	13
3	Comprehensive molecular diagnosis of 67 Chinese Usher syndrome probands: high rate of ethnicity specific mutations in Chinese USH patients 2015 ·Orphanet Journal of Rare Diseases ·Lichun Jiang, (unknown), Yumei Li, Jing Wang, Jacques Zaneveld, Hui Wang, (unknown), (unknown), Binbin Wang, Rui Chen, (unknown)	39
4	A Homozygous Missense Mutation in NEUROD1 Is Associated With Nonsyndromic Autosomal Recessive Retinitis Pigmentosa 2014 ·Investigative Ophthalmology & Visual Science ·Wang Fei, H. Li, Min Xu, Li Zhao, Lan Yang, Jacques Zaneveld, Keqing Wang, Yi Li, Ruifang Sui, Rui Chen	20
5	Next-generation sequencing-based molecular diagnosis of 82 retinitis pigmentosa probands from Northern Ireland 2014 ·Human Genetics ·Li Zhao, Feng Wang, Hui Wang, Yumei Li, (unknown), Keqing Wang, Colin E. Willoughby, Jacques Zaneveld, Lichun Jiang, Zachry T. Soens, (unknown), David Simpson, Giuliana Silvestri, Rui Chen	73
6	Genome-wide association scan in north Indians reveals three novel HLA-independent risk loci for ulcerative colitis 2014 ·Gut ·Garima Juyal, Sapna Negi, Ajit Sood, Aditi Gupta, Pushplata Prasad Singh, Sabyasachi Senapati, Jacques Zaneveld, Shalini Singh, Vandana Midha, Suzanne van Sommeren, Rinse K. Weersma, Jürg Ott, Sanjay K. Jain, Ramesh C. Juyal, B.K. Thelma	51
7	Comprehensive analysis of patients with Stargardt macular dystrophy reveals new genotype–phenotype correlations and unexpected diagnostic revisions 2014 ·Genetics in Medicine ·Jacques Zaneveld, Sorath Noorani Siddiqui, Huajin Li, Xia Wang, Hui Wang, Keqing Wang, Hui Li, Huanan Ren, Irma López, Allison Dorfman, Ayesha Khan, Feng Wang, Jason S. Salvo, Violet Gelowani, Yumei Li, Ruifang Sui, Robert K. Koenekoop, Rui Chen	41
8	TET2 mutations predict response to hypomethylating agents in myelodysplastic syndrome patients breakdown → 2014 ·Blood ·Rafael Bejar, Allegra M. Lord, Kristen E. Stevenson, Michal Bar‐Natan, Albert Pérez-Ladaga, Jacques Zaneveld, Hui Wang, Bennett Adam Caughey, Petar Stojanov, Gad Getz, Guillermo Garcia‐Manero, Hagop M. Kantarjian, Rui Chen, Richard M. Stone, Donna Neuberg, David P. Steensma, Benjamin L. Ebert	405
9	CGAP-Align: A High Performance DNA Short Read Alignment Tool 2013 ·PLoS ONE ·Yaoliang Chen, Ji Hyung Hong, Wanyun Cui, Jacques Zaneveld, Wei Wang, Richard A. Gibbs, Yanghua Xiao, Rui Chen	3
10	Dawn of ocular gene therapy: implications for molecular diagnosis in retinal disease 2013 ·Science China Life Sciences ·Jacques Zaneveld, Feng Wang, Xia Wang, Rui Chen	11
11	Next-Generation Sequencing–Based Molecular Diagnosis of a Chinese Patient Cohort With Autosomal Recessive Retinitis Pigmentosa 2013 ·Investigative Ophthalmology & Visual Science ·Qing Fu, Feng Wang, Hui Wang, Fei Xu, Jacques Zaneveld, Huanan Ren, Vafa Keser, Irma López, (unknown), Jason S. Salvo, Xia Wang, Li Zhao, Keqing Wang, Yumei Li, Robert K. Koenekoop, Rui Chen, Ruifang Sui	72
12	O-024 Next-generation sequencing of 213 MDS patient samples identifies mutation profiles associated with response to hypomethylating agents and overall survival 2013 ·Leukemia Research ·Rafael Bejar, Kristen E. Stevenson, Petar Stojanov, Jacques Zaneveld, Michal Bar‐Natan, Bennett Adam Caughey, (unknown), G. García-Manero, H. Kantarjian, Kristian Cibulskis, Gad Getz, David P. Steensma, R. M. Stone, (unknown), Donna Neuberg, Benjamin L. Ebert	5
13	Detection of Recurrent Mutations by Pooled Targeted Next-Generation Sequencing in MDS Patients Prior to Treatment with Hypomethylating Agents or Stem Cell Transplantation 2012 ·Blood ·Rafael Bejar, Kristen E. Stevenson, Petar Stojanov, Jacques Zaneveld, Michal Bar‐Natan, Bennett Adam Caughey, Hui Wang, Guillermo Garcia‐Manero, Hagop M. Kantarjian, Corey Cutler, Jerome Ritz, Kristian Cibulskis, Gad Getz, David P. Steensma, Richard M. Stone, Rui Chen, Donna Neuberg, Benjamin L. Ebert	7

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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