Hassan Chaı̈b

7.9k total citations · 1 hit paper
26 papers, 1.1k citations indexed

About

Hassan Chaı̈b is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, Hassan Chaı̈b has authored 26 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 6 papers in Sensory Systems and 4 papers in Genetics. Recurrent topics in Hassan Chaı̈b's work include Hearing, Cochlea, Tinnitus, Genetics (6 papers), Genomics and Chromatin Dynamics (5 papers) and Molecular Biology Techniques and Applications (4 papers). Hassan Chaı̈b is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (6 papers), Genomics and Chromatin Dynamics (5 papers) and Molecular Biology Techniques and Applications (4 papers). Hassan Chaı̈b collaborates with scholars based in United States, France and Canada. Hassan Chaı̈b's co-authors include Christine Petit, Jill A. Macoska, Mark A. Rubin, Parry Guilford, Sonia Abdelhak, J Hélias, Vasiliki Kalatzis, C. Vincent, Sylvie Compain and M Snyder and has published in prestigious journals such as Nature Genetics, Journal of Nutrition and Human Molecular Genetics.

In The Last Decade

Hassan Chaı̈b

25 papers receiving 1.1k citations

Hit Papers

Single-cell analyses define a continuum of cell state and... 2022 2026 2023 2024 2022 50 100 150
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.

  1. Single-cell analyses define a continuum of cell state and composition changes in the malignant transformation of polyps to colorectal cancer
    2022 154 citations Winston R. Becker, Stephanie Nevins et al. Nature Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Hassan Chaı̈b United States 16 638 295 163 137 130 26 1.1k
Margit Schraders Netherlands 20 717 1.1× 528 1.8× 249 1.5× 150 1.1× 386 3.0× 32 1.5k
Catherine B. Talmadge United States 12 1.1k 1.7× 248 0.8× 51 0.3× 88 0.6× 151 1.2× 19 1.4k
Laurence Delacroix Belgium 17 709 1.1× 148 0.5× 37 0.2× 159 1.2× 133 1.0× 27 1.0k
Robert S. Edinger United States 23 1.3k 2.0× 155 0.5× 243 1.5× 69 0.5× 72 0.6× 35 1.6k
Vittoria Carnicelli Italy 17 457 0.7× 53 0.2× 97 0.6× 224 1.6× 113 0.9× 47 1000
Silvia Vergarajauregui United States 17 598 0.9× 219 0.7× 89 0.5× 90 0.7× 43 0.3× 27 1.2k
Steve Stippec United States 19 1.5k 2.4× 67 0.2× 152 0.9× 142 1.0× 100 0.8× 28 1.9k
Jinghan Wang China 17 569 0.9× 149 0.5× 126 0.8× 149 1.1× 289 2.2× 41 881
Justin Ainscough United Kingdom 23 1.3k 2.1× 134 0.5× 103 0.6× 93 0.7× 230 1.8× 45 1.8k
Sascha E. Dho Canada 15 1.4k 2.3× 56 0.2× 121 0.7× 189 1.4× 69 0.5× 21 1.8k

Countries citing papers authored by Hassan Chaı̈b

Since Specialization
Citations

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

Fields of papers citing papers by Hassan Chaı̈b

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hassan Chaı̈b

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

All Works

20 of 20 papers shown
1.
Becker, Winston R., Stephanie Nevins, Derek C. Chen, et al.. (2022). Single-cell analyses define a continuum of cell state and composition changes in the malignant transformation of polyps to colorectal cancer. Nature Genetics. 54(7). 985–995. 154 indexed citations breakdown →
2.
Piening, Brian, Mengqi Zhang, Bao‐Li Loza, et al.. (2022). Whole transcriptome profiling of prospective endomyocardial biopsies reveals prognostic and diagnostic signatures of cardiac allograft rejection. The Journal of Heart and Lung Transplantation. 41(6). 840–848. 11 indexed citations
3.
Nguyen, Lan Huong, Wenyu Zhou, Rahul Sinha, et al.. (2020). Chromosome-level de novo assembly of the pig-tailed macaque genome using linked-read sequencing and HiC proximity scaffolding. GigaScience. 9(7). 9 indexed citations
4.
Peterson, Todd C., Kendra J. Lechtenberg, Brian Piening, et al.. (2020). Obesity Drives Delayed Infarct Expansion, Inflammation, and Distinct Gene Networks in a Mouse Stroke Model. Translational Stroke Research. 12(2). 331–346. 10 indexed citations
5.
Xu, Lei, Florette K. Hazard, Anne‐Flore Zmoos, et al.. (2014). Genomic analysis of fibrolamellar hepatocellular carcinoma. Human Molecular Genetics. 24(1). 50–63. 64 indexed citations
6.
Cooper, Carlton R., Bianca Graves, Hassan Chaı̈b, et al.. (2008). Novel surface expression of reticulocalbin 1 on bone endothelial cells and human prostate cancer cells is regulated by TNF‐α. Journal of Cellular Biochemistry. 104(6). 2298–2309. 29 indexed citations
7.
Chaı̈b, Hassan, Bethan E. Hoskins, Shazia Ashraf, et al.. (2007). Identification of BRAF as a new interactor of PLCε1, the protein mutated in nephrotic syndrome type 3. American Journal of Physiology-Renal Physiology. 294(1). F93–F99. 26 indexed citations
8.
Begley, Lesa, David Keeney, Ben Beheshti, et al.. (2005). Concordant copy number and transcriptional activity of genes mapping to derivative chromosomes 8 during cellular immortalization in vitro. Genes Chromosomes and Cancer. 45(2). 136–146. 16 indexed citations
9.
Macoska, Jill A., Pamela L. Paris, Colin C. Collins, et al.. (2004). Evolution of 8p loss in transformed human prostate epithelial cells. Cancer Genetics and Cytogenetics. 154(1). 36–43. 15 indexed citations
10.
Chaı̈b, Hassan, James W. MacDonald, Robert L. Vessella, et al.. (2003). Haploinsufficiency and reduced expression of genes localized to the 8p chromosomal region in human prostate tumors. Genes Chromosomes and Cancer. 37(3). 306–313. 20 indexed citations
11.
12.
Chaı̈b, Hassan, Mark A. Rubin, Neil R. Mucci, et al.. (2001). Activated in prostate cancer: a PDZ domain-containing protein highly expressed in human primary prostate tumors.. PubMed. 61(6). 2390–4. 38 indexed citations
13.
Mansour, Ahmad M., Mirna Mustapha, Hassan Chaı̈b, et al.. (1998). The Usher syndrome in the Lebanese population and further refinement of the USH2A candidate region. Human Genetics. 103(2). 193–198. 13 indexed citations
14.
Dodé, Catherine, Dominique Weil, Jacqueline Levilliers, et al.. (1998). Sequence Characterization of a Newly Identified Human α-Tubulin Gene (TUBA2). Genomics. 47(1). 125–130. 5 indexed citations
15.
Vincent, C., Vasiliki Kalatzis, Sonia Abdelhak, et al.. (1998). BOR and BO syndromes are allelic defects of EYA1.. PubMed. 5(4). 242–6. 92 indexed citations
16.
Chaı̈b, Hassan. (1997). A newly identified locus for Usher syndrome type I, USH1E, maps to chromosome 21q21. Human Molecular Genetics. 6(1). 27–31. 90 indexed citations
17.
Chaı̈b, Hassan. (1996). Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22. Human Molecular Genetics. 5(7). 1061–1064. 57 indexed citations
18.
19.
Chaı̈b, Hassan, Geneviève Lina‐Granade, Parry Guilford, et al.. (1994). A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval. Human Molecular Genetics. 3(12). 2219–2222. 66 indexed citations
20.
Guilford, Parry, Stéphane Blanchard, Hassan Chaı̈b, et al.. (1994). A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene. Human Molecular Genetics. 3(6). 989–993. 97 indexed citations

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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