Kimberly Chambert

Active 2008–2023

34
Papers
32,234
Citations
32
h-index
33
i10-index

Citations

Citations per year for Kimberly Chambert1974: 1 citations1992: 4 citations1995: 1 citations1999: 3 citations2000: 1 citations2002: 2 citations2003: 1 citations2004: 1 citations2007: 2 citations2008: 28 citations2009: 144 citations2010: 234 citations2011: 202 citations2012: 228 citations2013: 259 citations2014: 478 citations2015: 497 citations2016: 516 citations2017: 585 citations2018: 527 citations2019: 1,515 citations2020: 1,647 citations2021: 1,642 citations2022: 1,266 citations2023: 789 citations2024: 1,010 citations2025: 424 citations2026: 15 citations1975–1991: no citations, so these years are not shown1993–1994: no citations, so these years are not shown1996–1998: no citations, so these years are not shown2001: no citations, so this year is not shown2005–2006: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 4,942 citing papers, 24.3% of this breakdownUnited Kingdom: 2,072 citing papers, 10.2% of this breakdownGermany: 1,177 citing papers, 5.8% of this breakdownChina: 973 citing papers, 4.8% of this breakdownNetherlands: 941 citing papers, 4.6% of this breakdownAustralia: 911 citing papers, 4.5% of this breakdownCanada: 854 citing papers, 4.2% of this breakdownSweden: 718 citing papers, 3.5% of this breakdownItaly: 681 citing papers, 3.4% of this breakdownFrance: 586 citing papers, 2.9% of this breakdownSpain: 523 citing papers, 2.6% of this breakdownDenmark: 505 citing papers, 2.5% of this breakdown
0%24.3%Other 26.7%

Fields

  • Biochemistry, Genetics and Molecular Biology47.1%
  • Medicine29.4%
  • Neuroscience15.5%
  • Psychology4%
  • Immunology and Microbiology1.3%
  • Computer Science0.6%
  • Other2.1%

Topics

  • Genetic Associations and Epidemiology9%
  • Genetics and Neurodevelopmental Disorders4.8%
  • Genomic variations and chromosomal abnormalities3.5%
  • Acute Myeloid Leukemia Research3.4%
  • Autism Spectrum Disorder Research3.3%
  • Genomics and Rare Diseases3.3%
  • Other72.7%

Coauthors

All papers

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  1. Identification of common genetic risk variants for autism spectrum disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mads V. Hollegaard, Sigrun Hope, Daniel P. Howrigan, Hailiang Huang, Christina M. Hultman, Lambertus Klei, Julian Maller, Joanna Martin, Alicia R. Martin, Jennifer L. Moran, Mette Nyegaard, Terje Nærland, Duncan S. Palmer, Aarno Palotie, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy dPoterba, Jesper Buchhave Poulsen, Beaté St Pourcain, Per Qvist, Karola Rehnström, Abraham Reichenberg, Jennifer Reichert, Elise Robinson, Kathryn Roeder, Panos Roussos, Evald Sæmundsen, Sven Sandin, F. Kyle Satterstrom, George Davey Smith, Hreinn Stefánsson, Stacy Steinberg, Christine Stevens, Patrick F. Sullivan, Patrick Turley, G. Bragi Walters, Xinyi Xu, Kāri Stefánsson, Daniel H. Geschwind, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, Mark J. Daly, Anders D. Børglum - Nature Genetics 2019 cited by 2,632

  2. Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence

    Authors: , , , , , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2014 cited by 3,490

  3. Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Duncan S. Palmer, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy Poterba, Jesper Buchhave Poulsen, Stephan Ripke, Elise Robinson, F. Kyle Satterstrom, Hreinn Stefánsson, Christine Stevens, Patrick Turley, G. Bragi Walters, Hyejung Won, Margaret J. Wright, Ole A. Andreassen, Philip Asherson, Christie L. Burton, Dorret I. Boomsma, Bru Cormand, Søren Dalsgaard, Barbara Franke, Joel Gelernter, Daniel H. Geschwind, Håkon Håkonarson, Jan Haavik, Henry R. Kranzler, Jonna Kuntsi, K. Langley, Klaus‐Peter Lesch, Christel M. Middeldorp, Andreas Reif, Luís Augusto Rohde, Panos Roussos, Russell Schachar, Pamela Sklar, Edmund Sonuga‐Barke, Patrick F. Sullivan, Anita Thapar, Joyce Y. Tung, Irwin D. Waldman, Sarah E. Medland, Kāri Stefánsson, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Mark J. Daly, Stephen V. Faraone, Anders D. Børglum, Benjamin M. Neale - Nature Genetics 2018 cited by 2,320

  4. Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Clement C. Zai, Esben Agerbo, María J. Arranz, Philip Asherson, Marie Bækvad‐Hansen, Gísli Baldursson, Mark A. Bellgrove, Richard A. Belliveau, Jan K. Buitelaar, Christie L. Burton, Jonas Bybjerg‐Grauholm, Miguel Casas, Felecia Cerrato, Kimberly Chambert, Claire Churchhouse, Bru Cormand, Jennifer Crosbie, Søren Dalsgaard, Ditte Demontis, Alysa E. Doyle, Ashley Dumont, Josephine Elia, Jakob Grove, Ólafur Ó. Guðmundsson, Jan Haavik, Håkon Håkonarson, Christine Søholm Hansen, Catharina A. Hartman, Ziarih Hawi, Amaia Hervás, David M. Hougaard, Daniel P. Howrigan, Hailiang Huang, Jonna Kuntsi, K. Langley, Klaus‐Peter Lesch, Patrick W. L. Leung, Sandra K. Loo, Joanna Martin, Alicia R. Martin, James J. McGough, Sarah E. Medland, Jennifer L. Moran, Ole Mors, Preben Bo Mortensen, Robert D. Oades, Duncan S. Palmer, Carsten Bøcker Pedersen, Marianne G. Pedersen, Triinu Peters, Timothy Poterba, Jesper Buchhave Poulsen, Josep Antoni Ramos‐Quiroga, Andreas Reif, Marta Ribasés, Aribert Rothenberger, Paula Rovira, Cristina Sánchez‐Mora, F. Kyle Satterstrom, Russell Schachar, María Soler Artigas, Stacy Steinberg, Hreinn Stefánsson, Patrick Turley, G. Bragi Walters, Thomas Werge, Tetyana Zayats, Dan E. Arking, Francesco Bettella, Joseph D. Buxbaum and 506 more - Cell 2019 cited by 1,516

  5. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Hugh Gurling, Jennifer Stone, Kristin Ardlie, Jonathan Pimm, Stacey B. Gabriel, Robert Krasucki, Jacob Lawrence, Nicholas Bass, Derek W. Morris, Colm T. O’Dushlaine, Aiden Corvin, Finny G. Kuruvilla, Naomi R. Wray, Naomi R. Wray, Stuart MacGregor, Stuart MacGregor, Peter M. Visscher, Michael O‘Donovan, Michael O‘Donovan, Peter Holmans, Nadine Norton, Ivan Nikolov, Hywel Williams, George Kirov, Michael J. Owen, Lyudmila Georgieva, Michele T. Pato, Nick Craddock, Nigel Williams, Ayman Fanous, Patrick Sullivan, James A. Knowles, Patrick F. Sullivan, Jonathan Pimm, Jacob Lawrence, Hugh Gurling, Vinay Puri, Nicholas Bass, Andrew McQuillin, Khalid Choudhury, Robert Krasucki, Susmita Datta, Andrew McQuillin, Michael Gill, Elaine Kenny, Michael Gill - Nature 2009 cited by 5,069

  6. Genome-wide association study identifies 30 loci associated with bipolar disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nicholas Bass, Michael Bauer, Richard A. Belliveau, Sarah E. Bergen, Carsten Bøcker Pedersen, Erlend Bøen, Marco P. Boks, James Boocock, Monika Budde, William E. Bunney, Margit Burmeister, Jonas Bybjerg‐Grauholm, William Byerley, Miguel Casas, Felecia Cerrato, Pablo Cervantes, Kimberly Chambert, Alexander W. Charney, Danfeng Chen, Claire Churchhouse, Toni‐Kim Clarke, William Coryell, David W. Craig, Cristiana Cruceanu, David Curtis, Piotr M. Czerski, Anders M. Dale, Simone de Jong, Franziska Degenhardt, Jurgen Del‐Favero, J. Raymond DePaulo, Srdjan Djurovic, Amanda Dobbyn, Ashley Dumont, Torbjørn Elvsåshagen, Valentina Escott‐Price, Chun Chieh Fan, Sascha B. Fischer, Matthew Flickinger, Tatiana Foroud, Liz Forty, Josef Frank, Christine Fraser, Nelson B. Freimer, Louise Frisén, Katrin Gade, Diane Gage, Julie Garnham, Claudia Giambartolomei, Marianne Giørtz Pedersen, Jaqueline Goldstein, Scott D. Gordon, Katherine Gordon‐Smith, Elaine Green, Melissa J. Green, Tiffany A. Greenwood, Jakob Grove, Weihua Guan, José Guzmán‐Parra, Marian L. Hamshere, Martin Hautzinger, Urs Heilbronner, Stefan Herms, Maria Hipolito, Per Hoffmann, Dominic Holland, Laura M. Huckins, Stéphane Jamain, Jessica Johnson, Anders Juréus and 177 more - Nature Genetics 2019 cited by 1,627

  7. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Peter A Holmans, Ian Jones, George K Kirov, Sarah E. Bergen, Ivan Nikolov, Michael J Owen, Peter Holmans, Stanley Zammit, Katherine Gordon‐Smith, Nicholas Craddock, Lyudmila Georgieva, John S Witte, Detelina Grozeva, Ian D. Jones, Marian L. Hamshere, Ole A Andreassen, Srdjan Djurovic, Morten Mattingsdal, Michael O‘Donovan, Michael J. Owen, Anita Thapar, Robert C Thompson, Stanley J Watson, Nicholas Craddock, Lyudmila Georgieva, Nicholas Bass, Ian D. Jones, Hugh Gurling, Radhika Kandaswamy, Michael O‘Donovan, Michael J. Owen, Anita Thapar, Michael E. Goddard, Michael E. Goddard, Richard Anney, Devin Absher, Richard M. Myers, Ingrid Agartz, Srdjan Djurovic, Morten Mattingsdal, Ole A. Andreassen, Ingrid Melle, Ingrid Agartz, Robert C. Thompson, Stanley J. Watson, Huda Akil, Fan Meng, Farooq Amin, Ole A. Andreassen, Ingrid Melle, Robert Krasucki, Adebayo Anjorin, Khalid Choudhury, Jacob Lawrence, Hugh Gurling, Jonathan Pimm, Nicholas Bass, Radhika Kandaswamy, Andrew McQuillin, Vinay Puri, Elaine Kenny, Aiden Corvin, Paul Cormican, Derek W. Morris, Richard Anney, Emma M. Quinn, Gary Donohoe, Michael Gill, Louise Gallagher, Dan E. Arking and 270 more - Nature Genetics 2013 cited by 2,353

  8. De novo mutations in schizophrenia implicate synaptic networks

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Shaun Purcell, Michael O‘Donovan - Nature 2014 cited by 1,722

  9. Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , David Collier, Bryan J Mowry, Peter McGuffin, Anne Farmer, Jonna Kuntsi, Ian W. Craig, Stephen Newhouse, Stephen Newhouse, Katherine Gordon-Smith, Detelina Grozeva, Douglas M. Ruderfer, George K Kirov, Valentina Moskvina, Daniëlle Posthuma, Michael J Owen, Nigel Williams, Enda M. Byrne, Sang Lee, Nicholas Craddock, Naomi R. Wray, Pamela Sklar, Michael E Goddard, John S Witte, Tatiana Foroud, Daniel L Koller, Devin Absher, Richard M Myers, Anita Thapar, Ole A Andreassen, Ian Jones, Nigel Williams, Detelina Grozeva, Huda Akil, Peter Holmans, Michael J. Owen, Stanley J Watson, Farooq Amin, Adebayo Anjorin, Nicholas Bass, Khalid Choudhury, Hugh Gurling, Anita Thapar, Ian Jones, Nigel Williams, Pamela Sklar, Michael J. Owen, Vinay Puri, Richard Anney, Paul Cormican, Aiden Corvin, Gary J Donohoe, Louise Gallagher, John S. Witte, Daniel L. Koller, Tatiana Foroud, Richard M. Myers, Devin Absher, Srdjan Djurovic, Morten Mattingsdal, Maria H Azevedo, Ingrid Agartz, Lena Backlund, Ingrid Agartz, Huda Akil, Stanley J. Watson, Fan Meng, Robert C. Thompson, Farooq Amin, Tobias Banaschewski, Jack D Barchas and 275 more - Nature Neuroscience 2015 cited by 798

  10. Genome-wide association analysis identifies 13 new risk loci for schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kenneth S. Kendler, Kuang Lin, Derek W. Morris, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, F. Anthony O’Neill, Michael J. Owen, Milica Pejovic Milovancevic, Daniëlle Posthuma, John Powell, Alexander Richards, Brien P. Riley, Douglas M. Ruderfer, Dan Rujescu, Engilbert Sigurðsson, Teimuraz Silagadze, August B. Smit, Hreinn Stefánsson, Stacy Steinberg, Jaana Suvisaari, Sarah Tosato, Matthijs Verhage, James Walters, Elvira Bramon, Aiden Corvin, Michael O‘Donovan, Kari Stefansson, Edward M. Scolnick, Shaun Purcell, Steven A. McCarroll, Pamela Sklar, Christina M. Hultman, Patrick F. Sullivan - Nature Genetics 2013 cited by 1,565

  11. Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia

    Authors: , , , , , , , , , , , - Nature Neuroscience 2016 cited by 496

  12. De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Molecular Psychiatry 2011 cited by 877

  13. A polygenic burden of rare disruptive mutations in schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Steven A. McCarroll, Pamela Sklar - Nature 2014 cited by 1,461

  14. Discovery and Statistical Genotyping of Copy-Number Variation from Whole-Exome Sequencing Depth

    Authors: , , , , , , , , , , , , , , - The American Journal of Human Genetics 2012 cited by 597

  15. The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Swapnil Awasthi, Silviu‐Alin Bacanu, Judith A. Badner, Marie Bækvad‐Hansen, Jack D. Barchas, Nicholas Bass, Michael Bauer, Aartjan T.F. Beekman, Richard A. Belliveau, Sarah E. Bergen, Tim B. Bigdeli, Elisabeth B. Binder, Erlend Bøen, Marco P. Boks, James Boocock, Monika Budde, William Bunney, Margit Burmeister, Henriette N. Buttenschøn, Jonas Bybjerg‐Grauholm, William Byerley, Na Cai, Miguel Casas, Enrique Castelao, Felecia Cerrato, Pablo Cervantes, Kimberly Chambert, Alexander W. Charney, Danfeng Chen, Jane Christensen, Claire Churchhouse, David St Clair, Toni‐Kim Clarke, Lucía Colodro‐Conde, William Coryell, Baptiste Couvy‐Duchesne, David W. Craig, Gregory E. Crawford, Cristiana Cruceanu, Piotr M. Czerski, Anders M. Dale, Gail Davies, Ian J. Deary, Franziska Degenhardt, Jurgen Del‐Favero, J. Raymond DePaulo, Eske M. Derks, Neşe Direk, Srdjan Djurovic, Amanda Dobbyn, Conor V. Dolan, Ashley Dumont, Erin C. Dunn, Thalia C. Eley, Torbjørn Elvsåshagen, Valentina Escott‐Price, Chun Chieh Fan, Hilary K. Finucane, Sascha B. Fischer, Matthew Flickinger, Jerome C. Foo, Tatiana Foroud, Liz Forty, Josef Frank, Christine Fraser, Nelson B. Freimer, Louise Frisén, Katrin Gade, Diane Gage, Julie Garnham and 684 more - Biological Psychiatry 2019 cited by 210

  16. Quantifying prion disease penetrance using large population control cohorts

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jesús de Pedro‐Cuesta, Stéphane Haı̈k, Jean Laplanche, Élodie Bouaziz-Amar, J.-P. Brandel, Sabina Capellari, Piero Parchi, Anna Poleggi, Anna Ladogana, Anne O’Donnell‐Luria, Konrad J. Karczewski, Jamie L. Marshall, Michael Boehnke, Markku Laakso, Karen L. Mohlke, Anna K. Kähler, Kimberly Chambert, Steven A. McCarroll, Patrick F. Sullivan, Christina M. Hultman, Shaun Purcell, Pamela Sklar, Sven J. van der Lee, Annemieke J.M. Rozemüller, Casper Jansen, Albert Hofman, Robert Kraaij, Jeroen van Rooij, M. Arfan Ikram, André G. Uitterlinden, Cornelia M. van Duijn, Mark J. Daly, Daniel G. MacArthur - Science Translational Medicine 2016 cited by 469

  17. Exome sequencing in schizophrenia-affected parent–offspring trios reveals risk conferred by protein-coding de novo mutations

    Authors: , , , , , , , , , , , , , , , , , , , , , , , - Nature Neuroscience 2020 cited by 184

  18. Rare chromosomal deletions and duplications increase risk of schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Robert Krasucki, Jacob Lawrence, N J Bass, Douglas H. R. Blackwood, Walter J. Muir, Kevin A. McGhee, Ben Pickard, P. Malloy, AB MacLean, M. Van Beck, Aiden Corvin, M Gill, Derek W. Morris, Colm Ó'Dúshláine, Elaine Kenny, C M Hultman, Paul Lichtenstein, Emma F. Thelander, Carlos N. Pato, Michele T. Pato, Helena Medeiros, Celia Carvalho, A H Fanous, David Conti, James A. Knowles, David St Clair, Soh Leh Kwan, P F Sullivan, P F Sullivan, Stuart MacGregor, Peter M. Visscher, Draga Toncheva, Vihra Milanova, Waddington Jl, Srinivasa Thirumalai, Digby Quested, David Curtis, Caroline Crombie, Gillian Fraser, Nicholas Walker, Frank Middleton, Christopher Morley, Carlos Paz Ferreira, Antonio Macedo, M. Helena Azevedo - Nature 2008 cited by 1,512

  19. Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Paul Lichtenstein, Panos Roussos, James A. Knowles, Ian Jones, Lisa Jones, Christina M. Hultman, Roy H. Perlis, Shaun Purcell, Steven A. McCarroll, Carlos N. Pato, Michele T. Pato, Nick Craddock, Mikael Landén, Jordan W. Smoller, Pamela Sklar - Translational Psychiatry 2017 cited by 201

  20. Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Derek W. Morris, Amanda Elkin, Walter Muir, Kevin A. McGhee, Richard Williamson, Donald J. MacIntyre, Alan Maclean, David St Clair, Michelle Robinson, M. Van Beck, Ana Carla Pereira, Radhika Kandaswamy, Andrew McQuillin, David Collier, Nicholas Bass, Allan H. Young, Jacob Lawrence, I. Nicol Ferrier, Adebayo Anjorin, Anne Farmer, David Curtis, Edward M. Scolnick, Peter McGuffin, Mark J. Daly, Aiden Corvin, Peter Holmans, Douglas Blackwood, Hugh Gurling, Michael J. Owen, Shaun Purcell, Pamela Sklar, Nick Craddock - Nature Genetics 2008 cited by 1,258

  21. Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Richard A. Belliveau, Sarah E. Bergen, Carsten Bøcker Pedersen, Erlend Bøen, Marco P. Boks, James Boocock, Monika Budde, William E. Bunney, Margit Burmeister, Jonas Bybjerg‐Grauholm, William Byerley, Miguel Casas, Felecia Cerrato, Pablo Cervantes, Kimberly Chambert, Alexander W. Charney, Danfeng Chen, Claire Churchhouse, Toni‐Kim Clarke, William Coryell, David W. Craig, Cristiana Cruceanu, David Curtis, Piotr M. Czerski, Anders M. Dale, Simone de Jong, Franziska Degenhardt, Jurgen Del‐Favero, J. Raymond DePaulo, Srdjan Djurovic, Amanda Dobbyn, Ashley Dumont, Torbjørn Elvsåshagen, Valentina Escott‐Price, Chun Chieh Fan, Sascha B. Fischer, Matthew Flickinger, Tatiana Foroud, Liz Forty, Josef Frank, Christine Fraser, Nelson B Freimer, Louise Frisén, Katrin Gade, Diane Gage, Julie Garnham, Claudia Giambartolomei, Marianne Giørtz Pedersen, Jaqueline Goldstein, Scott D. Gordon, Katherine Gordon‐Smith, Elaine Green, Melissa J. Green, Tiffany A. Greenwood, Jakob Grove, Weihua Guan, JoséGuzman Parra, Marian L. Hamshere, Martin Hautzinger, Urs Heilbronner, Stefan Herms, Maria Hipolito, Per Hoffmann, Dominic Holland, Laura M. Huckins, Stéphane Jamain, Jessica Johnson, Anders Juréus, Radhika Kandaswamy, Robert Karlsson and 176 more - 2017 cited by 255

  22. Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia

    Authors: , , , , , , , , , , , - Neuron 2015 cited by 208

  23. Validation of Electronic Health Record Phenotyping of Bipolar Disorder Cases and Controls

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Carlos N. Pato, Michele T. Pato, Helen Medeiros, Janet Sobel, Nick Craddock, Ian Jones, Liz Forty, Arianna DiFlorio, Elaine Green, Lisa Jones, Katherine Dunjewski, Mikael Landén, Christina M. Hultman, Anders Juréus, Sarah E. Bergen, Oscar Svantesson, Steven A. McCarroll, Jennifer L. Moran, Jordan W. Smoller, Kimberly Chambert, Richard A. Belliveau - American Journal of Psychiatry 2014 cited by 159

  24. zCall: a rare variant caller for array-based genotyping: Genetics and population analysis

    Authors: , , , , , , , , , , , , , , , , - Bioinformatics, Bioinform. 2012 cited by 208