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Ward, Joey, Tunbridge, Elizabeth M., Sandor, Cynthia, Lyall, Laura M., Ferguson, Amy, Strawbridge, Rona J., Lyall, Donald M., Cullen, Breda, Graham, Nicholas, Johnston, Keira J. A., Webber, Caleb, Escott-Price, Valentina, O'Donovan, Michael, Pell, Jill P., Bailey, Mark E. S., Harrison, Paul J. and Smith, Daniel J.
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The genomic basis of mood instability: identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function.
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Mencacci, Niccolò, Reynolds, Regina, Garcia Ruiz, Sonia, Vandrovcova, Jana, Forabosco, Paola, Sánchez-Ferrer, Alvaro, Volpato, Viola, Weale, Michael E., Bhatia, Kailash P., Webber, Caleb, Hardy, John, Botía, Juan and Ryten, Mina
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Agarwal, Devika, Sandor, Cynthia, Volpato, Viola, Caffrey, Tara M., Monzon Sandoval, Jimena, Bowden, Rory, Alegre-Abarrategui, Javier, Wade-Martins, Richard and Webber, Caleb
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A single-cell atlas of the human substantia nigra reveals cell-specific pathways associated with neurological disorders.
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Hedegaard, Anne, Monzón-Sandoval, Jimena, Newey, Sarah E., Whiteley, Emma S., Webber, Caleb and Akerman, Colin J.
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Monzón‐Sandoval, Jimena, Poggiolini, Ilaria, Ilmer, Tobias, Wade-Martins, Richard, Webber, Caleb and Parkkinen, Laura
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Williams, Nigel M., Hubbard, Leon, Sandor, Cynthia, Webber, Caleb, Hendry, Hannah, Lawton, Michael, Carroll, Camille, Chaudhuri, K. Ray, Morris, Huw, Hu, Michele T., Grosset, Donald G., Kobylecki, Christopher and Silverdale, Monty 2020. Genome‐wide association study of pain in Parkinson's disease implicates TRPM8 as a risk factor. Movement Disorders 35 (4) , pp. 705-707. 10.1002/mds.28001 |
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Volpato, Viola and Webber, Caleb
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Addressing variability in iPSC-derived models of human disease: guidelines to promote reproducibility.
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Booth, Heather D.E., Wessely, Frank, Connor-Robson, Natalie, Rinaldi, Federica, Vowles, Jane, Browne, Cathy, Evetts, Samuel G., Hu, Michele T., Cowley, Sally A., Webber, Caleb and Wade-Martins, Richard
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Collins, Stephan C., Mikhaleva, Anna, Vrcelj, Katarina, Vancollie, Valerie E., Wagner, Christel, Demeure, Nestor, Whitley, Helen, Kannan, Meghna, Balz, Rebecca, Anthony, Lauren F. E., Edwards, Andrew, Moine, Hervé, White, Jacqueline K., Adams, David J., Reymond, Alexandre, Lelliott, Christopher J., Webber, Caleb and Yalcin, Binnaz
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Eddowes, Lucy A., Al-Hourani, Kinda, Ramamurthy, Narayan, Frankish, Jamie, Baddock, Hannah T, Sandor, Cynthia, Ryan, John D., Fusco, Dahlene N., Arezes, João, Giannoulatou, Eleni, Boninsegna, Sara, Chevaliez, Stephane, Owens, Benjamin M. J., Sun, Chia Chi, Fabris, Paolo, Giordani, Maria Teresa, Martines, Diego, Vukicevic, Slobodan, Crowe, John, Lin, Herbert Y., Rehwinkel, Jan, McHugh, Peter J., Binder, Marco, Babitt, Jodie L., Chung, Raymond T., Lawless, Matthew W., Armitage, Andrew E., Webber, Caleb, Klenerman, Paul and Drakesmith, Hal 2018. Antiviral activity of bone morphogenetic proteins and activins. Nature Microbiology 4 , pp. 339-351. 10.1038/s41564-018-0301-9 |
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Sandor, Cynthia, Robertson, Paul, Lang, Charmaine, Heger, Andreas, Booth, Heather, Vowles, Jane, Witty, Lorna, Bowden, Rory, Hu, Michele, Cowley, Sally A., Wade-Martins, Richard and Webber, Caleb
2017.
Transcriptomic profiling of purified patient-derived dopamine neurons identifies convergent perturbations and therapeutics for Parkinson's disease.
Human Molecular Genetics
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10.1093/hmg/ddw412
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Sandor, Cynthia, Honti, Frantisek, Haerty, Wilfried, Szewczyk-Krolikowski, Konrad, Tomlinson, Paul, Evetts, Sam, Millin, Stephanie, Keane, Thomas, McCarthy, Shane A., Durbin, Richard, Talbot, Kevin, Hu, Michele, Webber, Caleb, Ponting, Chris P. and Wade-Martins, Richard
2017.
Whole-exome sequencing of 228 patients with sporadic Parkinson's disease.
Scientific Reports
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Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S., Palta, Proot, Esko, Tonu, Pers, Tune H., Farh, Kai-How, Cuenca-Leon, Ester, Muona, Mikko, Furlotte, Nicholas A., Kurth, Tobias, Ingason, Andres, McMahon, George, Ligthart, Lannie, Terwindt, Gisela M., Kallela, Mikko, Freilinger, Tobias M., Ran, Caroline, Gordon, Scott G., Stam, Annie H., Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H. H., Lehtimäki, Terho, Sarin, Antti-Pekka, Wedenoja, Juho, Hinds, David A., Buring, Julie E., Schürks, Markus, Ridker, Paul M., Gudlaug Hrafnsdottir, Maria, Stefansson, Hreinn, Ring, Susan M., Hottenga, Jouke-Jan, Penninx, Brenda W. J. H., Färkkilä, Markus, Artto, Ville, Kaunisto, Mari, Vepsäläinen, Salli, Malik, Rainer, Heath, Andrew C., Madden, Pamela A. F., Martin, Nicholas G., Montgomery, Grant W., Kurki, Mitja I., Kals, Mart, Mägi, Reedik, Pärn, Kalle, Hämäläinen, Eija, Huang, Hailiang, Byrnes, Andrea E., Franke, Lude, Huang, Jie, Stergiakouli, Evie, Lee, Phil H., Sandor, Cynthia, Webber, Caleb, Cader, Zameel, Mullter-Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Eriksson, Johan G., Salomaa, Veikko, Heikkilä, Kauko, Loehrer, Elizabeth, Uitterlinden, Andre, Hofman, Albert, van Duijn, Cornelia M., Cherkas, Lynn, Pedersen, Linda M., Stubhaug, Audun, Nielsen, Christopher S., Männikkö, Minna, Mihailov, Evelin, Milani, Liki, Göbel, Hartmut, Esserlind, Ann-Louise, Christensen, Anne Francke, Hansen, Thomas Folkmann, Werge, Thomas, International Headache Genetics Consortium, , Kaprio, Jaakko, Aromaa, Arpo J., Raitakari, Olli, Ikram, M. Arfan, Spector, Tim, Järvelin, Marjo-Riitta, Metspalu, Andres, Kubisch, Christian, Strachan, David P., Ferrari, Michel D., Belin, Andrea C., Dichgans, Martin, Wessman, Jaiha, van den Maagdenberg, Arn M. J. M., Zwart, John-Anker, Boomsma, Dorret I., Smith, George Davey, Stefansson, Kari, Eriksson, Nicholas, Daly, Mark J., Neale, Benjamin M., Olesen, Jes, Chasman, Daniel I., Nyholt, Dale R. and Palotie, Aarno 2016. Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics 48 (10) , p. 1296. 10.1038/ng1016-1296c |
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Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S., Palta, Priit, Esko, Tonu, Pers, Tune H., Farh, Kai-How, Cuenca-Leon, Ester, Muona, Mikko, Furlotte, Nicholas A., Kurth, Tobais, Ingason, Andres, McMahon, George, Ligthart, Lannie, Terwindt, Gisela M., Kallela, Mikko, Freilinger, Tobias M., Ran, Caroline, Gordon, Scott G., Stam, Anine H., Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H. H., Lehtimäki, Terho, Sarin, Anti-Pekka, Wedenoja, Juho, Hinds, David A., Buring, Julie E., Schürks, Markus, Ridker, Paul M., Hrafnsdottir, Maria Gudlaug, Stefansson, Hreinn, Ring, Susan M., Hottenga, Jouke-Jan, Penninx, Brenda W. J. H., Färkkilä, Markus, Artto, Ville, Mari, Kaunisto, Vepsäläinen, Salli, Malik, Rainer, Heath, Andrew C., Madden, Pamela A. F., Martin, Nicholas G., Montgomery, Grant W., Kurki, Mitja I., Kals, Mart, Mägi, Reedik, Pärn, Kalle, Hämäläinen, Eija, Huang, Hailiang, Byrnes, Andrea E., Franke, Lude, Huang, Jie, Stergiakouli, Evie, Lee, Phil H., Sandor, Cynthia, Webber, Caleb, Cader, Zameel, Muller-Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Eriksson, Johan G., Salomaa, Veikko, Heikkilä, Kauko, Loehrer, Elizabeth, Uitterlinden, Andre G., Hofman, Albert, van Duijn, Cornelia M., Cherkas, Lynn, Pedersen, Linda, Stubhaug, Audun, Nielsen, Christopher S., Männikkö, Minna, Mihailov, Evelin, Milani, Liki, Göbel, Hartmut, Esserlind, Ann-Louise, Christensen, Anne Francke, Hansen, Thomas Folkmann, Wege, Thomas, International Headache Genetics Consortium, , Kaprio, Jaakko, Aromaa, Arpo J., Raitakari, Olli, Ikram, M. Arfan, Spector, Tim, Järvelin, Marjo-Riitta, Metspalu, Andres, Kubisch, Christian, Strachan, David P., Ferrari, Michel D., Belin, Andrea C., Dichgans, Martin, Wessman, Maija, van den Maagdenberg, Arn M. J. M., Zwart, John-Anker, Boomsma, Dorret I., Smith, George Davey, Stefansson, Kari, Eriksson, Nicholas, Daly, Mark J., Neale, Benjamin M., Olesen, Jes, Chasman, Daniel I., Nyhol, Dale R. and Palotie, Aarno 2016. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics 48 (8) , pp. 856-866. 10.1038/ng.3598 |
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Kochinke, Korinna, Zweier, Christiane, Nijhof, Bonnie, Fenckova, Michaela, Cizek, Pavel, Honti, Frank, Keerthikumar, Shivakumar, Oortveld, Merel A. W., Kleefstra, Tjitske, Kramer, Jamie M., Webber, Caleb, Huynen, Martijn A. and Schenck, Annette 2016. Systematic phenomics analysis deconvolutes genes mutated in intellectual disability into biologically coherent modules. American Journal of Human Genetics 98 (1) , pp. 149-164. 10.1016/j.ajhg.2015.11.024 |
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Tan, Jennifer Y., Sirey, Tamara, Honti, Frantisek, Graham, Bryony, Piovesan, Allison, Merkenschlager, Matthias, Webber, Caleb, Ponting, Chris P. and Marques, Ana C.
2015.
Corrigendum: Extensive microRNA-mediated crosstalk between lncRNAs and mRNAs in mouse embryonic stem cells.
Genome Research
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10.1101/gr.196568.115
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Steinberg, Julia, Honti, Frantisek, Meader, Stephen and Webber, Caleb
2015.
Haploinsufficiency predictions without study bias.
Nucleic Acids Research
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Andrews, Tallulah, Honti, Frantisek, Pfundt, Rolph, De Leeuw, Nicole, Hehir-Kwa, Jayne, Silfhout, Anneke Vulto-cvan, De Vries, Bert and Webber, Caleb
2015.
The clustering of functionally related genes contributes to CNV-mediated disease.
Genome Research
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10.1101/gr.184325.114
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Tan, Jennifer Y., Sirey, Tamara, Honti, Frantisek, Graham, Byrony, Piovesan, Allison, Merkenschlager, Matthias, Webber, Caleb, Ponting, Chris P. and Marques, Ana C.
2015.
Extensive microRNA-mediated crosstalk between lncRNAs and mRNAs in mouse embryonic stem cells.
Genome Research
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10.1101/gr.181974.114
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Grice, Stuart J., Liu, Ji-Long and Webber, Caleb
2015.
Synergistic interactions between Drosophila orthologues of genes spanned by De Novo human CNVs support multiple-hit models of autism.
PLoS Genetics
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10.1371/journal.pgen.1004998
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Andrews, Tallulah, Meader, Stephen, Vulto-van Silfhout, Anneke, Taylor, Avigail, Steinberg, Juila, Hehir-Kwa, Jayne, Pfundt, Rolph, de Leeuw, Nicole, de Vries, Bert B.A. and Webber, Caleb
2015.
Gene networks underlying convergent and pleiotropic phenotypes in a large and systematically-phenotyped cohort with heterogeneous developmental disorders.
PLoS Genetics
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10.1371/journal.pgen.1005012
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Taylor, Avigail, Steinberg, Julia and Webber, Caleb
2015.
Duplications in ADHD patients harbour neurobehavioural genes that are co-expressed with genes associated with hyperactivity in the mouse.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
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Taylor, Avigail, Steinberg, Julia, Andrews, Tallulah S. and Webber, Caleb
2015.
GeneNet toolbox for MATLAB: a flexible platform for the analysis of gene connectivity in biological networks.
Bioinformatics
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Honti, Frantisek, Meader, Stephen and Webber, Caleb
2014.
Unbiased functional clustering of gene variants with a phenotypic-linkage network.
PLoS Computational Biology
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10.1371/journal.pcbi.1003815
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Ferry, Quentin, Steinberg, Julia, Webber, Caleb, FitzPatrick, David R., Ponting, Chris P., Zisserman, Andrew and Nell?ker, Christoffer
2014.
Diagnostically relevant facial gestalt information from ordinary photos.
eLife
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10.7554/eLife.02020.001
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Robinson, Peter N. and Webber, Caleb
2014.
Phenotype ontologies and cross-species analysis for translational research.
PLoS Genetics
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10.1371/journal.pgen.1004268
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Vulto-van Silfhout, Anneke T., Hehir-Kwa, Jayne Y., van Bon, Bregje W. M., Schuurs-Hoeijmakers, Janneke H M., Meader, Stephen, Hellebrekers, Claudia J. M., Thoonen, Ilse J. M., de Brouwer, Arjan P. M., Brunner, Han G., Webber, Caleb, Pfundt, Rolph, de Leeuw, Nicole and De Vries, Bert B. A. 2013. Clinical significance of de novo and inherited copy-number variation. Human Mutation 34 (12) , pp. 1679-1687. 10.1002/humu.22442 |
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Steinberg, Julia and Webber, Caleb
2013.
The roles of FMRP-regulated genes in autism spectrum disorder: single- and multiple-hit genetic etiologies.
American Journal of Human Genetics
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10.1016/j.ajhg.2013.09.013
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Brandler, William M., Morris, Andrew P., Evans, David M., Scerri, Thomas S., Kemp, John P., Timpson, Nicholas J., St Pourcain, Beate, Smith, George Davey, Ring, Susan M., Stein, John, Monaco, Anthony P., Talcott, Joel B., Fisher, Simon E., Webber, Caleb and Paracchini, Silvia
2013.
Common variants in left/right asymmetry genes and pathways are associated with relative hand skill.
PLoS Genetics
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10.1371/journal.pgen.1003751
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Heger, Andreas, Webber, Caleb, Goodson, Martin, Ponting, Chris P. and Lunter, Gerton
2013.
GAT: A simulation framework for testing the association of genomic intervals.
Bioinformatics
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10.1093/bioinformatics/btt343
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Noh, Hyun Ji, Ponting, Chris P., Boulding, Hannah C., Meader, Stephen, Betancur, Catalina, Buxbaum, Joseph D., Pinto, Dalila, Marshall, Christian R., Lionel, Anath C., Scherer, Stephen W. and Webber, Caleb
2013.
Network topologies and convergent aetiologies arising from deletions and duplications observed in individuals with autism.
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10.1371/journal.pgen.1003523
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Hoerder-Suabedissen, Anna, Oeschger, Franziska M., Krishnan, Michelle L., Belgard, T. Grant, Wang, Wei Zhi, Lee, Sheena, Webber, Caleb, Petretto, Enrico, Edwards, A. David and Molnár, Zoltán 2013. Expression profiling of mouse subplate reveals a dynamic gene network and disease association with autism and schizophrenia. Proceedings of the National Academy of Sciences 110 (9) , pp. 3555-3560. 10.1073/pnas.1218510110 |
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Boulding, Hannah and Webber, Caleb 2012. Large-scale objective association of mouse phenotypes with human symptoms through structural variation identified in patients with developmental disorders. Human Mutation 33 (5) , pp. 874-883. 10.1002/humu.22069 |
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Webber, Caleb 2011. Functional enrichment analysis with structural variants: pitfalls and strategies. Cytogenetic and Genome Research 135 (3-4) , pp. 277-285. 10.1159/000331670 |
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Mills, Ryan E., Pittard, W. Stephen, Mullaney, Julienne M., Farooq, Umar, Creasy, Todd H., Mahurkar, Anup A., Kemeza, David M., Strassler, Daniel S., Ponting, Chris P., Webber, Caleb and Devine, Scott E. 2011. Natural genetic variation caused by small insertions and deletions in the human genome. Genome Research 21 (6) , pp. 830-839. 10.1101/gr.115907.110 |
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Shaikh, Tamim H., Haldeman-Englert, Chad, Geiger, Elizabeth A., Ponting, Chris P. and Webber, Caleb 2011. Genes and biological processes commonly disrupted in rare and heterogeneous developmental delay syndromes. Human Molecular Genetics 20 (5) , pp. 880-893. 10.1093/hmg/ddq527 |
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Agam, Avigail, Yalcin, Binnaz, Bhomra, Amarjit, Cubin, Matthew, Webber, Caleb, Holmes, Christopher, Flint, Jonathan and Mott, Richard
2010.
Elusive copy number variation in the mouse genome.
PLoS ONE
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Hehir-Kwa, Jayne Y., Wieskamp, Nienke, Webber, Caleb, Pfundt, Rolph, Brunner, Han G., Gilissen, Christian, de Vries, Bert B. A., Ponting, Chris P. and Veltman, Joris A.
2010.
Accurate distinction of pathogenic from benign CNVs in mental retardation.
PLoS Computational Biology
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10.1371/journal.pcbi.1000752
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Webber, Caleb, Hehir-Kwa, Jayne Y., Nguyen, Duc-Quang, De Vries, Bert B. A., Veltman, Joris A. and Ponting, Chris P.
2009.
Forging links between human mental retardation-associated CNVs and mouse gene knockout models.
PLoS Genetics
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10.1371/journal.pgen.1000531
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Nguyen, Duc-Quang, Webber, Caleb, Hehir-Kwa, Jayne, Pfundt, Rolph, Veltman, Joris and Ponting, Chris P. 2008. Reduced purifying selection prevails over positive selection in human copy number variant evolution. Genome Research 18 (11) , pp. 1711-1723. 10.1101/gr.077289.108 |
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Walsh, Thomas P., Webber, Caleb, Searle, Stephen, Sturrock, Shane S. and Barton, Geoffrey J.
2008.
SCANPS: a web server for iterative protein sequence database searching by dynamic programing, with display in a hierarchical SCOP browser.
Nucleic Acids Research
36
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10.1093/nar/gkn320
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Warren, Wesley C., Hillier, LaDeana W., Marshall Graves, Jennifer A., Birney, Ewan, Ponting, Chris P., Grützner, Frank, Belov, Katherine, Miller, Webb, Clarke, Laura, Chinwalla, Asif T., Yang, Shiaw-Pyng, Heger, Andreas, Locke, Devin P., Miethke, Pat, Waters, Paul D., Veyrunes, Frédéric, Fulton, Lucinda, Fulton, Bob, Graves, Tina, Wallis, John, Puente, Xose S., López-Otín, Carlos, Ordóñez, Gonzalo R., Eichler, Evan E., Chen, Lin, Cheng, Ze, Deakin, Jenine E., Aslop, Amber, Thompson, Katherine, Kirby, Patrick, Papenfuss, Anthony T., Wakefield, Matthew J., Olender, Tsviya, Lancet, Doron, Huttley, Gavin A., Smit, Arian F. A., Pask, Andrew, Temple-Smith, Peter, Batzer, Mark A., Walker, Jerilyn A., Konkel, Miriam K., Harris, Robert S., Whittington, Camilla M., Wong, Emily S. W., Gemmell, Neil J., Buschiazzo, Emmanuel, Vargas Jentzsch, Iris M., Merkel, Angelika, Schmitz, Juergen, Zemann, Anja, Churakov, Gennady, Kriegs, Jan Ole, Brosius, Juergen, Murchison, Elizabeth P., Sachidanandam, Ravi, Smith, Carly, Hannon, Gregory J., Tsend-Ayush, Enkhjargal, McMillan, Daniel, Attenborough, Rosalind, Rens, Willem, Ferguson-Smith, Malcolm, Lefèvre, Christophe M., Sharp, Julie A., Nicholas, Kevin R., Ray, David A., Kube, Michael, Reinhardt, Richard, Pringle, Thomas H., Taylor, James, Jones, Russell C., Nixon, Brett, Dacheux, Jean-Louis, Niwa, Hitoshi, Sekita, Yoko, Huang, Xiaoqiu, Stark, Alexander, Kheradpour, Pouya, Kellis, Manolis, Flicek, Paul, Chen, Yuan, Webber, Caleb, Hardison, Ross, Nelson, Joanne, Hallsworth-Pepin, Kym, Delehaunty, Kim, Markovic, Chris, Minx, Pat, Feng, Yucheng, Kremitzki, Colin, Mitreva, Makedonka, Glasscock, Jarret, Wylie, Todd, Wohldmann, Patricia, Thiru, Prathapan, Nhan, Michael N., Pohl, Craig S., Smith, Scott M., Hour, Shungfeng, renfree, Marilyn B., Mardis, Elaine R. and Wilson, Richard K.
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Genome analysis of the platypus reveals unique signatures of evolution.
Nature
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Goodstadt, Leo, Heger, Andreas, Webber, Caleb and Ponting, Chris P.
2007.
An analysis of the gene complement of a marsupial, Monodelphis domestica: evolution of lineage-specific genes and giant chromosomes.
Genome Research
17
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10.1101/gr.6093907
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Mikkelsen, Tarjei S., Wakefield, Mattew J., Aken, Bronwen, Amemiya, Chris T., Chang, Jean L., Duke, Sahannon, Garber, Manuel, Gentles, Andrew J., Goodstadt, Leo, Heger, Andreas, Jurka, Jerzy, Kamal, Michael, Mauceli, Evan, Searle, Stephen M. J., Sharpe, Ted, Baker, Michelle L., Batzer, Mark A., Benos, Panayiotis, Belov, Katherine, Clamp, Michele, Cook, April, Cuff, James, Das, Radhika, Davidow, Lance, Deakin, Janine E., Fazzari, Melissa J., Glass, Jacob L., Grabherr, Manfred, Greally, John M., Gu, Wanjun, Hore, Timothy A., Huttley, Gavin A., Kleber, Michael, Jirtle, Randy L., Koina, Edda, Lee, Jeannie T., Mahony, Shaun, Marra, Marco A., Miller, Robert D., Nicholls, Robert D., Oda, Mayumi, Papenfuss, Anthony T., Parra, Zuly E., Pollock, David D., Ray, David A., Schein, Jacqueline E., Speed, Terence P., Thompson, Katherine, VandeBerg, John L., Wade, Claire M., Walker, Jerilyn A., Waters, Paul D., Webber, Caleb, Weidman, Jennifer R., Xie, Xiaohui, Zody, Michael C., Broad Institute Genome Sequencing Platform, , Broad Institute Whole Genome Assembly Team, , Marshall Graves, Jennier A., Ponting, Chris P., Breen, Matthew, Samollow, Paul B., Lander, Eric S. and Lindbald-Toh, Kerstin
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Genome of the marsupial Monodelphis domestica reveals innovation in non-coding sequences.
Nature
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Nguyen, Duc-Quang, Webber, Caleb and Ponting, Chris P.
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Bias of selection on human copy-number variants.
PLoS Genetics
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Webber, Caleb and Ponting, Chris P. 2005. Hotspots of mutation and breakage in dog and human chromosomes. Genome Research 15 (12) , pp. 1787-1797. 10.1101/gr.3896805 |
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