खोज परिणाम - Kimberly Chambert

परिणाम को परिष्कृत करें
  1. 1
    Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia

    Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia द्वारा Andrew Pocklington, Elliott Rees, James Walters, Jun Han, David H. Kavanagh, Kimberly Chambert, Peter Holmans, Jennifer L. Moran, Steven A. McCarroll, George Kirov, Michael O’Donovan, Michael J. Owen

    प्रकाशित 2015
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  2. 2
    Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia

    Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia द्वारा Giulio Genovese, Menachem Fromer, Eli A. Stahl, Douglas M. Ruderfer, Kimberly Chambert, Mikael Landén, Jennifer L. Moran, Shaun Purcell, Pamela Sklar, Patrick F. Sullivan, Christina M. Hultman, Steven A. McCarroll

    प्रकाशित 2016
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  3. 3
    Using population admixture to help complete maps of the human genome

    Using population admixture to help complete maps of the human genome द्वारा Giulio Genovese, Robert E. Handsaker, Heng Li, Nicolas Altemose, Amelia M. Lindgren, Kimberly Chambert, Bogdan Paşaniuc, Alkes L. Price, David Reich, Cynthia C. Morton, Martin R. Pollak, James G. Wilson, Steven A. McCarroll

    प्रकाशित 2013
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  4. 4
    Cis-acting regulation of brain-specific ANK3 gene expression by a genetic variant associated with bipolar disorder

    Cis-acting regulation of brain-specific ANK3 gene expression by a genetic variant associated with bipolar disorder द्वारा Erroll H. Rueckert, Douglas Barker, Douglas M. Ruderfer, Sarah E. Bergen, Colm O’Dushlaine, Catherine J. Luce, Steven D. Sheridan, Kraig M. Theriault, Kimberly Chambert, Jennifer L. Moran, Shaun Purcell, Jon M. Madison, Stephen J. Haggarty, Pamela Sklar

    प्रकाशित 2012
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  5. 5
    Discovery and Statistical Genotyping of Copy-Number Variation from Whole-Exome Sequencing Depth

    Discovery and Statistical Genotyping of Copy-Number Variation from Whole-Exome Sequencing Depth द्वारा Menachem Fromer, Jennifer L. Moran, Kimberly Chambert, Eric Banks, Sarah E. Bergen, Douglas M. Ruderfer, Robert E. Handsaker, Steven A. McCarroll, Michael O’Donovan, Michael J. Owen, George Kirov, Patrick F. Sullivan, Christina M. Hultman, Pamela Sklar, Shaun Purcell

    प्रकाशित 2012
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  6. 6
    zCall: a rare variant caller for array-based genotyping

    zCall: a rare variant caller for array-based genotyping द्वारा Jacqueline I. Goldstein, Andrew Crenshaw, Jason Carey, George Grant, Jared Maguire, Menachem Fromer, Colm O’Dushlaine, Jennifer L. Moran, Kimberly Chambert, Christine Stevens, Pamela Sklar, Christina M. Hultman, Shaun Purcell, Steven A. McCarroll, Patrick F. Sullivan, Mark J. Daly, Benjamin M. Neale

    प्रकाशित 2012
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  7. 7
    Cryptic and Complex Chromosomal Aberrations in Early-Onset Neuropsychiatric Disorders

    Cryptic and Complex Chromosomal Aberrations in Early-Onset Neuropsychiatric Disorders द्वारा Harrison Brand, Vamsee Pillalamarri, Ryan L. Collins, Stacey Eggert, Colm Ó'Dúshláine, Ellen B. Braaten, Matthew R. Stone, Kimberly Chambert, Nathan D. Doty, Carrie Hanscom, Jill A. Rosenfeld, Hillary L. Ditmars, Jessica E. Blais, Ryan E. Mills, Charles Lee, James F. Gusella, Steven A. McCarroll, Jordan W. Smoller, Michael E. Talkowski, Alysa E. Doyle

    प्रकाशित 2014
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  8. 8
    Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence

    Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence द्वारा Giulio Genovese, Anna K. Kähler, Robert E. Handsaker, Johan Lindberg, Samuel A. Rose, Samuel F. Bakhoum, Kimberly Chambert, Eran Mick, Benjamin M. Neale, Menachem Fromer, Shaun Purcell, Oscar Svantesson, Mikael Landén, Martin Höglund, Sören Lehmann, Stacey B. Gabriel, Jennifer L. Moran, Eric S. Lander, Patrick F. Sullivan, Pamela Sklar, Henrik Grönberg, Christina M. Hultman, Steven A. McCarroll

    प्रकाशित 2014
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  9. 9
    Characterization of bipolar disorder patient-specific induced pluripotent stem cells from a family reveals neurodevelopmental and mRNA expression abnormalities

    Characterization of bipolar disorder patient-specific induced pluripotent stem cells from a family reveals neurodevelopmental and mRNA expression abnormalities द्वारा Jon M. Madison, Fangjian Zhou, Aparna Nigam, Ali Hussain, Douglas Barker, Ralda Nehme, Karlijn van der Ven, Jonathan Y. Hsu, Pavlina Wolf, Morgan Fleishman, C O'Dushlaine, Samuel A. Rose, Kimberly Chambert, Frank H. Lau, Tim Ahfeldt, Erroll H. Rueckert, Steven D. Sheridan, Daniel M. Fass, James Nemesh, Thomas E. Mullen, Laurence Dahéron, Steven A. McCarroll, Pamela Sklar, Roy H. Perlis, Stephen J. Haggarty

    प्रकाशित 2015
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  10. 10
    Exome sequencing in schizophrenia-affected parent–offspring trios reveals risk conferred by protein-coding de novo mutations

    Exome sequencing in schizophrenia-affected parent–offspring trios reveals risk conferred by protein-coding de novo mutations द्वारा Daniel P. Howrigan, Samuel A. Rose, Kaitlin E. Samocha, Menachem Fromer, Felecia Cerrato, Wei J. Chen, Claire Churchhouse, Kimberly Chambert, Sharon D. Chandler, Mark J. Daly, Ashley Dumont, Giulio Genovese, Hai‐Gwo Hwu, Nan M. Laird, Jack A. Kosmicki, Jennifer L. Moran, Cheryl Roe, Tarjinder Singh, Shi‐Heng Wang, Stephen V. Faraone, Stephen J. Glatt, Steven A. McCarroll, Ming T. Tsuang, Benjamin M. Neale

    प्रकाशित 2020
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  11. 11
    De novo mutations in schizophrenia implicate synaptic networks

    De novo mutations in schizophrenia implicate synaptic networks द्वारा Menachem Fromer, Andrew Pocklington, David H. Kavanagh, Hywel Williams, Sarah Dwyer, Padhraig Gormley, Lyudmila Georgieva, Elliott Rees, Priit Palta, Douglas M. Ruderfer, Noa Carrera, Isla Humphreys, Jessica Johnson, Panos Roussos, Douglas Barker, Eric Banks, Vihra Milanova, Seth G. N. Grant, Eilís Hannon, Samuel A. Rose, Kimberly Chambert, Milind Mahajan, Edward M. Scolnick, Jennifer L. Moran, George Kirov, Aarno Palotie, Steven A. McCarroll, Peter Holmans, Pamela Sklar, Michael J. Owen, Shaun Purcell, Michael O’Donovan

    प्रकाशित 2014
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  12. 12
    De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia

    De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia द्वारा George Kirov, Andrew Pocklington, Peter Holmans, Dobril Ivanov, Masashi Ikeda, Douglas M. Ruderfer, Jennifer L. Moran, Kimberly Chambert, Драга Тончева, L. Georgieva, Detelina Grozeva, Marija Fjodorova, R Wollerton, Elliott Rees, Ivan Nikolov, Louie N. van de Lagemaat, Àlex Bayés, E Fernández, Pall I. Olason, Yvonne Böttcher, Noboru H. Komiyama, Mark O. Collins, Jyoti S. Choudhary, Kāri Stefánsson, Hreinn Stefánsson, Seth G. N. Grant, Shaun Purcell, Pamela Sklar, Michael O’Donovan, Michael J. Owen

    प्रकाशित 2011
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  13. 13
    A polygenic burden of rare disruptive mutations in schizophrenia

    A polygenic burden of rare disruptive mutations in schizophrenia द्वारा Shaun Purcell, Jennifer L. Moran, Menachem Fromer, Douglas M. Ruderfer, Nadia Solovieff, Panos Roussos, Colm Ó'Dúshláine, Kimberly Chambert, Sarah E. Bergen, Anna K. Kähler, Laramie E. Duncan, Eli Stahl, Giulio Genovese, Esperanza Fernández, Mark O. Collins, Noboru H. Komiyama, Jyoti S. Choudhary, Patrik K. E. Magnusson, Eric Banks, Khalid Shakir, Kiran Garimella, Tim Fennell, Mark A. DePristo, Seth G. N. Grant, Stephen J. Haggarty, Stacey Gabriel, Edward M. Scolnick, Eric S. Lander, Christina M. Hultman, Patrick F. Sullivan, Steven A. McCarroll, Pamela Sklar

    प्रकाशित 2014
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  14. 14
    Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder

    Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder द्वारा Alexander W. Charney, Douglas M. Ruderfer, Eli A. Stahl, Jennifer L. Moran, Kimberly Chambert, Rich Belliveau, Liz Forty, Katherine Gordon‐Smith, Arianna Di Florio, P H Lee, Evelyn J. Bromet, P.F. Buckley, Michael Escamilla, Ayman H. Fanous, Laura J. Fochtmann, Douglas S. Lehrer, Dolores Malaspina, Stephen R. Marder, Christopher P. Morley, Humberto Nicolini, Diana O. Perkins, Jeffrey J. Rakofsky, Mark Hyman Rapaport, Helena Medeiros, Janet L. Sobell, E K Green, Lena Backlund, Sarah E. Bergen, Anders Juréus, Martin Schalling, 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

    प्रकाशित 2017
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  15. 15
    Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases

    Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases द्वारा Alexander W. Charney, Eli A. Stahl, Elaine Green, Chia‐Yen Chen, Jennifer L. Moran, Kimberly Chambert, Richard A. Belliveau, Liz Forty, Katherine Gordon‐Smith, Sang Hyuck Lee, Evelyn J. Bromet, P.F. Buckley, Michael Escamilla, Ayman H. Fanous, Laura J. Fochtmann, Douglas S. Lehrer, Dolores Malaspina, Stephen R. Marder, Christopher P. Morley, Humberto Nicolini, Diana O. Perkins, Jeffrey J. Rakofsky, Mark Hyman Rapaport, Helena Medeiros, Janet L. Sobell, Lena Backlund, Sarah E. Bergen, Anders Juréus, Martin Schalling, Paul Lichtenstein, James A. Knowles, Katherine E. Burdick, Ian Jones, Lisa Jones, Christina M. Hultman, Roy H. Perlis, Shaun Purcell, Steven A. McCarroll, Carlos N. Pato, Michele T. Pato, Ariana Di Florio, Nick Craddock, Mikael Landén, Jordan W. Smoller, Douglas M. Ruderfer, Pamela Sklar

    प्रकाशित 2018
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  16. 16
    Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder

    Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder द्वारा Jie Song, Sarah E. Bergen, Arianna Di Florio, Robert Karlsson, Alexander W. Charney, Douglas M. Ruderfer, Eli A. Stahl, Kimberly D. Chambert, Jennifer L. Moran, Katherine Gordon‐Smith, Liz Forty, E K Green, Ian Jones, Lisa Jones, Edward M. Scolnick, Pamela Sklar, Jordan W. Smoller, Paul Lichtenstein, Christina M. Hultman, Nicholas Craddock, M Landén, Jordan W. Smoller, Roy H. Perlis, Phil Hyoun Lee, Víctor M. Castro, Alison G. Hoffnagle, Pamela Sklar, Eli A. Stahl, Shaun Purcell, Douglas M. Ruderfer, Alexander W. Charney, Panos Roussos, Carlos Pato Michele Pato, Helen Medeiros, Janet Sobel, Nick Craddock, Ian Jones, Liz Forty, Arianna Di Florio, Elaine Green, Lisa Jones, Katherine Gordon‐Smith, Mikael Landén, Christina M. Hultman, Anders Juréus, Sarah E. Bergen, Steven A. McCarroll, Jennifer L. Moran, Jordan W. Smoller, Kimberly Chambert, Richard A. Belliveau

    प्रकाशित 2015
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  17. 17
    Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity

    Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity द्वारा Veera M. Rajagopal, Andrea Ganna, Jonathan R. I. Coleman, Andrea G. Allegrini, Georgios Voloudakis, Jakob Grove, Thomas D. Als, Henriette Thisted Horsdal, Liselotte Petersen, Vivek Appadurai, Andrew J. Schork, Alfonso Buil, Cynthia M. Bulik, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, David M. Hougaard, Ole Mors, Merete Nordentoft, Thomas Werge, Rich Belliveau, Caitlin E. Carey, Felecia Cerrato, Kimberly Chambert, Tracy Air, Mark J. Daly, Ashley Dumont, Jacqueline I. Goldstein, Christine Søholm Hansen, Daniel P. Howrigan, Hailiang Huang, Julian Maller, Alicia R. Martin, Joanna Martin, Manuel Mattheisen, Jennifer L. Moran, Benjamin M. Neale, Jonatan Pallesen, Duncan S. Palmer, Carsten Bcker Pedersen, Marianne Giørtz Pedersen, Timothy Poterba, Stephan Ripke, F. Kyle Satterstrom, Wesley K. Thompson, Patrick Turley, Raymond K. Walters, Preben Bo Mortensen, Gerome Breen, Panos Roussos, Robert Plomin, Esben Agerbo, Anders D. Børglum, Ditte Demontis

    प्रकाशित 2023
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  18. 18
    Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

    Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder द्वारा Manuel A. R. Ferreira, Michael O’Donovan, Yan Meng, Ian Jones, Douglas M. Ruderfer, Lisa Jones, Jinbo Fan, George Kirov, Roy H. Perlis, Elaine Green, Jordan W. Smoller, Detelina Grozeva, Jennifer Stone, Ivan Nikolov, Kimberly Chambert, Marian L. Hamshere, Vishwajit L. Nimgaonkar, Valentina Moskvina, Michael E. Thase, Sian Caesar, Gary S. Sachs, Jennifer Franklin, Katherine Gordon‐Smith, Kristin G. Ardlie, Stacey Gabriel, Christine Fraser, Brendan Blumenstiel, Matthew DeFelice, Gerome Breen, Michael Gill, 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

    प्रकाशित 2008
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  19. 19
    Genome-wide association analysis identifies 13 new risk loci for schizophrenia

    Genome-wide association analysis identifies 13 new risk loci for schizophrenia द्वारा Stephan Ripke, Colm Ó'Dúshláine, Kimberly Chambert, Jennifer L. Moran, Anna K. Kähler, Susanne Akterin, Sarah E. Bergen, Ann L. Collins, James J. Crowley, Menachem Fromer, Yunjung Kim, Sang Lee, Patrik K. E. Magnusson, Nick Sanchez, Eli A. Stahl, Stephanie Williams, Naomi R. Wray, Kai Xia, Francesco Bettella, Anders D. Børglum, Brendan Bulik‐Sullivan, Paul Cormican, Nick Craddock, Christiaan de Leeuw, Naser Durmishi, Michael Gill, В. Е. Голимбет, Marian L. Hamshere, Peter Holmans, David M Hougaard, Kenneth S. Kendler, Kuang Lin, Derek W. Morris, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, F. Anthony O’Neill, Michael J. Owen, Miloš Milovančević, 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, Hreinn Stefánsson, Edward M. Scolnick, Shaun Purcell, Steven A. McCarroll, Pamela Sklar, Christina M. Hultman, Patrick F. Sullivan

    प्रकाशित 2013
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  20. 20
    Quantifying prion disease penetrance using large population control cohorts

    Quantifying prion disease penetrance using large population control cohorts द्वारा Eric Vallabh Minikel, Sonia M. Vallabh, Monkol Lek, Karol Estrada, Kaitlin E. Samocha, J. Fah Sathirapongsasuti, Cory Y. McLean, Joyce Y. Tung, Linda P. C. Yu, Pierluigi Gambetti, Janis Blevins, Shulin Zhang, Yvonne Cohen, Wei Chen, Masahito Yamada, Tsuyoshi Hamaguchi, Nobuo Sanjo, Hidehiro Mizusawa, Yosikazu Nakamura, Tetsuyuki Kitamoto, Steven Collins, Alison Boyd, Robert Will, Richard Knight, Claudia Ponto, Inga Zerr, Theo F. J. Kraus, Sabina Eigenbrod, Armin Giese, Miguel Calero, Jesús de Pedro‐Cuesta, Stéphane Haı̈k, Jean Laplanche, Elodie 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

    प्रकाशित 2016
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