Caleb Webber

17.8k citations

58 papers · 3.0k indexed · h-index 28

Impact in

Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Developmental Neuroscience top 5%

Papers in ⓘ

Genetics 29
- Genomic variations and chromosomal abnormalities 18
- Genomics and Rare Diseases 16
- Genetic Associations and Epidemiology 7
Neurology 6
- Parkinson's Disease Mechanisms and Treatments 6

Co-authors: Chris P. Ponting (16 shared papers)Viola Volpato (5 shared papers)Julia Steinberg (6 shared papers)Richard Wade‐Martins (7 shared papers)Jimena Monzón‐Sandoval (8 shared papers)Andreas Heger (4 shared papers)Rory Bowden (5 shared papers)Cynthia Sandor (6 shared papers)
Journals: PLoS Genetics (8 papers)Genome Research (7 papers)Bioinformatics (4 papers)Human Molecular Genetics (3 papers)PLoS Computational Biology (3 papers)
Partner nations: United Kingdom Netherlands United States

In The Last Decade

Caleb Webber

58 papers receiving 2.9k citations

Peers

Countries citing papers authored by Caleb Webber

Since Specialization

Citations

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

Fields of papers citing papers by Caleb Webber

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Caleb Webber, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Caleb Webber Line = papers co-authored together Caleb Webber links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 58 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Addressing variability in iPSC-derived models of human disease: guidelines to promote reproducibility Disease Models & Mechanisms ·Viola Volpato, Caleb Webber	2020	228
2	Bias of Selection on Human Copy-Number Variants PLoS Genetics ·Duc-Quang Nguyen, Caleb Webber, Chris P. Ponting	2006	203
3	Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules The American Journal of Human Genetics ·Korinna Kochinke, Christiane Zweier, Bonnie Nijhof, Michaela Fencková, Pavel Čížek, Frank Honti, Shivakumar Keerthikumar, Merel A.W. Oortveld, Tjitske Kleefstra, Jamie M. Kramer, Caleb Webber, Martijn A. Huynen, Annette Schenck	2016	189
4	A single-cell atlas of the human substantia nigra reveals cell-specific pathways associated with neurological disorders Nature Communications ·Devika Agarwal, Cynthia Sandor, Viola Volpato, Tara M. Caffrey, Jimena Monzón‐Sandoval, Rory Bowden, Javier Alegre‐Abarrategui, Richard Wade‐Martins, Caleb Webber	2020	187
5	Natural genetic variation caused by small insertions and deletions in the human genome Genome Research ·Ryan E. Mills, W. Stephen Pittard, Julienne M. Mullaney, Umar Farooq, Todd Creasy, Anup Mahurkar, David M. Kemeza, Daniel S. Strassler, Chris P. Ponting, Caleb Webber, Scott E. Devine	2011	179
6	GAT: a simulation framework for testing the association of genomic intervals Bioinformatics ·Andreas Heger, Caleb Webber, Martin Goodson, Chris P. Ponting, Gerton Lunter	2013	153
7	Common Variants in Left/Right Asymmetry Genes and Pathways Are Associated with Relative Hand Skill PLoS Genetics ·William M. Brandler, Andrew P. Morris, David M. Evans, Thomas Scerri, John P. Kemp, Nicholas J. Timpson, Beaté St Pourcain, George Davey Smith, Susan M. Ring, John Stein, Anthony P. Monaco, Joel B. Talcott, Simon E. Fisher, Caleb Webber, Silvia Paracchini	2013	115
8	Single-Cell Sequencing of iPSC-Dopamine Neurons Reconstructs Disease Progression and Identifies HDAC4 as a Regulator of Parkinson Cell Phenotypes Cell stem cell ·Charmaine Lang, Kieran R. Campbell, Brent J. Ryan, Phillippa J. Carling, Moustafa Attar, Jane Vowles, Olga V. Perestenko, Rory Bowden, Fahd Baig, Meike Kasten, (unknown), Sally A. Cowley, Caleb Webber, Richard Wade‐Martins	2018	106
9	Cellular α-synuclein pathology is associated with bioenergetic dysfunction in Parkinson’s iPSC-derived dopamine neurons Human Molecular Genetics ·Federico Zambon, Marta Cherubini, Hugo J. R. Fernandes, Charmaine Lang, Brent J. Ryan, Viola Volpato, Nora Bengoa‐Vergniory, Siv Vingill, Moustafa Attar, Heather Booth, Walther Haenseler, Jane Vowles, Rory Bowden, Caleb Webber, Sally A. Cowley, Richard Wade‐Martins	2019	103
10	Diagnostically relevant facial gestalt information from ordinary photos eLife ·Quentin R. V. Ferry, Julia Steinberg, Caleb Webber, David Fitzpatrick, Chris P. Ponting, Andrew Zisserman, Christoffer Nellåker	2014	97
11	Expression profiling of mouse subplate reveals a dynamic gene network and disease association with autism and schizophrenia Proceedings of the National Academy of Sciences ·Anna Hoerder‐Suabedissen, Franziska M. Oeschger, Michelle L. Krishnan, T. Grant Belgard, Weizhi Wang, Sheena Lee, Caleb Webber, Enrico Petretto, A. David Edwards, Zoltán Molnár	2013	89
12	Extensive microRNA-mediated crosstalk between lncRNAs and mRNAs in mouse embryonic stem cells Genome Research ·Jennifer Y. Tan, Tamara Sirey, Frantisek Honti, Bryony Graham, Allison Piovesan, Matthias Merkenschlager, Caleb Webber, Chris P. Ponting, Ana Claudia Marques	2015	88
13	SCANPS: a web server for iterative protein sequence database searching by dynamic programing, with display in a hierarchical SCOP browser Nucleic Acids Research ·Terence P. Walsh, Caleb Webber, Stephen M. J. Searle, Shane Sturrock, Geoffrey J. Barton	2008	82
14	Clinical Significance of De Novo and Inherited Copy-Number Variation Human Mutation ·Anneke T. Vulto-van Silfhout, Jayne Y. Hehir‐Kwa, Bregje W.M. van Bon, Janneke Schuurs-Hoeijmakers, Stephen Meader, Claudia J.M. Hellebrekers, Ilse J.M. Thoonen, Arjan P.M. de Brouwer, Han G. Brunner, Caleb Webber, Rolph Pfundt, Nicole de Leeuw, Bert de Vries	2013	79
15	Reduced purifying selection prevails over positive selection in human copy number variant evolution Genome Research ·Duc-Quang Nguyen, Caleb Webber, Jayne Y. Hehir‐Kwa, Rolph Pfundt, Joris A. Veltman, Chris P. Ponting	2008	68
16	RNA sequencing reveals MMP2 and TGFB1 downregulation in LRRK2 G2019S Parkinson's iPSC-derived astrocytes Neurobiology of Disease ·Heather Booth, Frank Wessely, Natalie Connor‐Robson, Federica Rinaldi, Jane Vowles, Cathy Browne, Samuel Evetts, (unknown), Sally A. Cowley, Caleb Webber, Richard Wade‐Martins	2019	54
17	Transcriptomic profiling of purified patient-derived dopamine neurons identifies convergent perturbations and therapeutics for Parkinson’s disease Human Molecular Genetics ·Cynthia Sandor, Paul Robertson, Charmaine Lang, Andreas Heger, Heather Booth, Jane Vowles, Lorna Witty, Rory Bowden, (unknown), Sally A. Cowley, Richard Wade‐Martins, Caleb Webber	2016	51
18	The Roles of FMRP-Regulated Genes in Autism Spectrum Disorder: Single- and Multiple-Hit Genetic Etiologies The American Journal of Human Genetics ·Julia Steinberg, Caleb Webber	2013	47
19	Phenotype Ontologies and Cross-Species Analysis for Translational Research PLoS Genetics ·Peter N. Robinson, Caleb Webber	2014	47
20	Pro-maturational Effects of Human iPSC-Derived Cortical Astrocytes upon iPSC-Derived Cortical Neurons Stem Cell Reports ·Anne Hedegaard, Jimena Monzón‐Sandoval, Sarah E. Newey, Emma Whiteley, Caleb Webber, Colin J. Akerman	2020	44

About Caleb Webber

Caleb Webber is a scholar working on Genetics, Neurology, Molecular Biology, Developmental Neuroscience and Cellular and Molecular Neuroscience, having authored 58 papers that have together received 3.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (18 papers), Genomics and Rare Diseases (16 papers), Congenital heart defects research (10 papers), Single-cell and spatial transcriptomics (7 papers), Genomics and Phylogenetic Studies (7 papers), Genetic Associations and Epidemiology (7 papers), Parkinson's Disease Mechanisms and Treatments (6 papers) and RNA Research and Splicing (6 papers). The work is most often cited by research in Genetics (1.2k citations), Developmental Neuroscience (135 citations), Neurology (263 citations), Molecular Biology (1.7k citations) and Cellular and Molecular Neuroscience (377 citations). Caleb Webber has collaborated with scholars based in United Kingdom, Netherlands and United States. Frequent co-authors include Chris P. Ponting, Viola Volpato, Julia Steinberg, Richard Wade‐Martins, Jimena Monzón‐Sandoval, Andreas Heger, Rory Bowden, Cynthia Sandor, Geoffrey J. Barton and Jayne Y. Hehir‐Kwa. Their work appears in journals such as PLoS Genetics, Genome Research, Bioinformatics, Human Molecular Genetics and PLoS Computational Biology.

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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