Hassan Chaı̈b

7.9k citations

26 papers · 1.1k indexed · 1 hit paper · h-index 16

Co-authors: Christine Petit Jill A. Macoska Mark A. Rubin Parry Guilford Sonia Abdelhak J Hélias Vasiliki Kalatzis C. Vincent
Topics: Hearing, Cochlea, Tinnitus, Genetics (6 papers)Genomics and Chromatin Dynamics (5 papers)Molecular Biology Techniques and Applications (4 papers)
Cited by: Sensory Systems Neurology Molecular Biology
Journals: Nature Genetics Journal of Nutrition Human Molecular Genetics
Partner nations: United States France Canada

In The Last Decade

Hassan Chaı̈b

25 papers receiving 1.1k citations

Hit Papers

align trajectories

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.

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

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Single-cell analyses define a continuum of cell state and composition changes in the malignant transformation of polyps to colorectal cancerbreakdown → 2022 ·Nature Genetics ·Winston R. Becker,Stephanie Nevins,Derek C. Chen,Roxanne Chiu,Aaron M. Horning,Tuhin K. Guha,Rozelle Laquindanum,Meredith Mills,Hassan Chaı̈b,Uri Ladabaum,Teri A. Longacre,Jeanne Shen,Edward D. Esplin,Anshul Kundaje,James M. Ford,Christina Curtis,M Snyder,William J. Greenleaf	154
2	Whole transcriptome profiling of prospective endomyocardial biopsies reveals prognostic and diagnostic signatures of cardiac allograft rejection 2022 ·The Journal of Heart and Lung Transplantation ·Brian Piening,(unknown),Mengqi Zhang,Bao‐Li Loza,(unknown),Hui Gao,Maedeh Mohebnasab,(unknown),(unknown),Eric Wei,(unknown),(unknown),Hassan Chaı̈b,Nancy K. Sweitzer,Mario C. Deng,Alexandre C. Pereira,Martín Cadeiras,Abraham Shaked,M Snyder,Brendan J. Keating	11
3	Chromosome-level de novo assembly of the pig-tailed macaque genome using linked-read sequencing and HiC proximity scaffolding 2020 ·GigaScience ·(unknown),(unknown),Lan Huong Nguyen,Wenyu Zhou,Rahul Sinha,Hayan Lee,John B. Hanks,(unknown),Lihua Jiang,Ruiqi Jian,Ho-Yong Lee,Giltae Song,Hassan Chaı̈b,(unknown),Serafim Batzoglou,Susan Holmes,David Glenn Smith,Joseph L. Mankowski,Stefan Prost,M Snyder	9
4	Obesity Drives Delayed Infarct Expansion, Inflammation, and Distinct Gene Networks in a Mouse Stroke Model 2020 ·Translational Stroke Research ·Todd C. Peterson,Kendra J. Lechtenberg,Brian Piening,(unknown),Eric Wei,Hassan Chaı̈b,(unknown),M Snyder,Marion S. Buckwalter	10
5	Genomic analysis of fibrolamellar hepatocellular carcinoma 2014 ·Human Molecular Genetics ·Lei Xu,Florette K. Hazard,Anne‐Flore Zmoos,Nadine S. Jahchan,Hassan Chaı̈b,Phillip M. Garfin,Arun Rangaswami,M Snyder,Julien Sage	64
6	Novel surface expression of reticulocalbin 1 on bone endothelial cells and human prostate cancer cells is regulated by TNF‐α 2008 ·Journal of Cellular Biochemistry ·Carlton R. Cooper,Bianca Graves,(unknown),Hassan Chaı̈b,Jill E. Lynch,(unknown),(unknown),Luc Van Kaer,(unknown),Kirk J. Czymmek,(unknown),Carlton D. Donald,Katia Sol‐Church,(unknown),Babette B. Weksler,Mary C. Farach‐Carson,Jill A. Macoska,Robert A. Sikes,Kenneth J. Pienta	29
7	Identification of BRAF as a new interactor of PLCε1, the protein mutated in nephrotic syndrome type 3 2007 ·American Journal of Physiology-Renal Physiology ·Hassan Chaı̈b,Bethan E. Hoskins,Shazia Ashraf,Meera Goyal,Roger C. Wiggins,Friedhelm Hildebrandt	26
8	Concordant copy number and transcriptional activity of genes mapping to derivative chromosomes 8 during cellular immortalization in vitro 2005 ·Genes Chromosomes and Cancer ·Lesa Begley,David Keeney,Ben Beheshti,Jeremy A. Squire,(unknown),Hassan Chaı̈b,James W. MacDonald,Johng S. Rhim,Jill A. Macoska	16
9	Evolution of 8p loss in transformed human prostate epithelial cells 2004 ·Cancer Genetics and Cytogenetics ·Jill A. Macoska,Pamela L. Paris,Colin C. Collins,Armann Andaya,Ben Beheshti,Hassan Chaı̈b,(unknown),Lesa Begley,James W. MacDonald,Jeremy A. Squire	15
10	Haploinsufficiency and reduced expression of genes localized to the 8p chromosomal region in human prostate tumors 2003 ·Genes Chromosomes and Cancer ·Hassan Chaı̈b,James W. MacDonald,Robert L. Vessella,Joseph Washburn,Janna E. Quinn,(unknown),Mark A. Rubin,Jill A. Macoska	20
11	Profiling and Verification of Gene Expression Patterns in Normal and Malignant Human Prostate Tissues by cDNA Microarray Analysis 2001 ·Neoplasia ·Hassan Chaı̈b,(unknown),Mark A. Rubin,Jill A. Macoska	96
12	Activated in prostate cancer: a PDZ domain-containing protein highly expressed in human primary prostate tumors. 2001 ·PubMed ·Hassan Chaı̈b,Mark A. Rubin,Neil R. Mucci,(unknown),Jeremy M. G. Taylor,Mark L. Day,Johng S. Rhim,Jill A. Macoska	38
13	The Usher syndrome in the Lebanese population and further refinement of the USH2A candidate region 1998 ·Human Genetics ·(unknown),Ahmad M. Mansour,(unknown),(unknown),Mirna Mustapha,Hassan Chaı̈b,Alexandre Nehme,André Mégarbané,Jacques Loiselet,Christine Petit,Rima Slim	13
14	Sequence Characterization of a Newly Identified Human α-Tubulin Gene (TUBA2) 1998 ·Genomics ·Catherine Dodé,Dominique Weil,Jacqueline Levilliers,Fabien Crozet,Hassan Chaı̈b,Fabienne Lévi-Acobas,Parry Guilford,Christine Petit	5
15	BOR and BO syndromes are allelic defects of EYA1. 1998 ·PubMed ·C. Vincent,Vasiliki Kalatzis,Sonia Abdelhak,Hassan Chaı̈b,Sylvie Compain,J Hélias,(unknown),Christine Petit	92
16	A newly identified locus for Usher syndrome type I, USH1E, maps to chromosome 21q21 1997 ·Human Molecular Genetics ·Hassan Chaı̈b	90
17	Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22 1996 ·Human Molecular Genetics ·Hassan Chaı̈b	57
18	A YAC Contig and an EST Map in the Pericentromeric Region of Chromosome 13 Surrounding the Loci for Neurosensory Nonsyndromic Deafness (DFNB1 and DFNA3) and Limb-Girdle Muscular Dystrophy Type 2C (LGMD2C) 1995 ·Genomics ·Parry Guilford,Catherine Dodé,Fabien Crozet,Stéphane Blanchard,Hassan Chaı̈b,Jacqueline Levilliers,Fabienne Lévi-Acobas,Dominique Weil,Jean Weissenbach,Daniel Cohen,Denis Le Paslier,Jean‐Claude Kaplan,Christine Petit	24
19	A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval 1994 ·Human Molecular Genetics ·Hassan Chaı̈b,Geneviève Lina‐Granade,Parry Guilford,Henri Plauchu,Jacqueline Levilliers,A Morgon,Christine Petit	66
20	A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene 1994 ·Human Molecular Genetics ·Parry Guilford,(unknown),Stéphane Blanchard,Hassan Chaı̈b,Denis Le Paslier,Jean Weissenbach,Mohamed Drira,Christine Petit	97

About Hassan Chaı̈b

Hassan Chaı̈b is a scholar working on Sensory Systems, Transplantation and Cancer Research, having authored 26 papers that have together received 1.1k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (6 papers), Genomics and Chromatin Dynamics (5 papers) and Molecular Biology Techniques and Applications (4 papers). The work is most often cited by research in Sensory Systems (295 citations), Neurology (94 citations) and Molecular Biology (638 citations). Hassan Chaı̈b has collaborated with scholars based in United States, France and Canada. Frequent 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. Their work appears in journals such as Nature Genetics, Journal of Nutrition and Human Molecular Genetics.

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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