Torthaí cuardaigh - Lambertus Klei

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  1. 1
    A Simple Method for Weighted Bending of Genetic (Co)variance Matrices

    A Simple Method for Weighted Bending of Genetic (Co)variance Matrices de réir H. Jorjani, Lambertus Klei, Ulf Emanuelson

    Foilsithe / Cruthaithe 2003
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  2. 2
    Semisoft clustering of single-cell data

    Semisoft clustering of single-cell data de réir Lingxue Zhu, Jing Lei, Lambertus Klei, Bernie Devlin, Kathryn Roeder

    Foilsithe / Cruthaithe 2018
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  3. 3
    Discovering genetic ancestry using spectral graph theory

    Discovering genetic ancestry using spectral graph theory de réir Ann B. Lee, Diana Luca, Lambertus Klei, Bernie Devlin, Kathryn Roeder

    Foilsithe / Cruthaithe 2009
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  4. 4
    An interactome perturbation framework prioritizes damaging missense mutations for developmental disorders

    An interactome perturbation framework prioritizes damaging missense mutations for developmental disorders de réir Siwei Chen, Robert Fragoza, Lambertus Klei, Yuan Liu, Jiebiao Wang, Kathryn Roeder, Bernie Devlin, Haiyuan Yu

    Foilsithe / Cruthaithe 2018
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  5. 5
    Functional connectome fingerprinting accuracy in youths and adults is similar when examined on the same day and 1.5‐years apart

    Functional connectome fingerprinting accuracy in youths and adults is similar when examined on the same day and 1.5‐years apart de réir Maria Jalbrzikowski, Fuchen Liu, William Foran, Lambertus Klei, Finnegan J. Calabro, Kathryn Roeder, Bernie Devlin, Beatríz Luna

    Foilsithe / Cruthaithe 2020
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  6. 6
    On the Use of General Control Samples for Genome-wide Association Studies: Genetic Matching Highlights Causal Variants

    On the Use of General Control Samples for Genome-wide Association Studies: Genetic Matching Highlights Causal Variants de réir Diana Luca, Steven Ringquist, Lambertus Klei, Ann B. Lee, Christian Gieger, H.‐Erich Wichmann, Stefan Schreiber, Michael Krawczak, Ying Lu, Alexis Styche, Bernie Devlin, Kathryn Roeder, Massimo Trucco

    Foilsithe / Cruthaithe 2008
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  7. 7
    Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden

    Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden de réir Benjamin Hon Kei Yip, Dan Bai, Behrang Mahjani, Lambertus Klei, Yudi Pawitan, Christina M. Hultman, Dorothy E. Grice, Kathryn Roeder, Joseph D. Buxbaum, Bernie Devlin, Abraham Reichenberg, Sven Sandin

    Foilsithe / Cruthaithe 2017
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  8. 8
    Genome-wide Transcriptome Profiling Reveals the Functional Impact of Rare De Novo and Recurrent CNVs in Autism Spectrum Disorders

    Genome-wide Transcriptome Profiling Reveals the Functional Impact of Rare De Novo and Recurrent CNVs in Autism Spectrum Disorders de réir Rui Luo, Stephan Sanders, Yuan Tian, Irina Voineagu, Ni Huang, Su H. Chu, Lambertus Klei, Chaochao Cai, Jing Ou, Jennifer K. Lowe, Matthew E. Hurles, Bernie Devlin, Matthew W. State, Daniel H. Geschwind

    Foilsithe / Cruthaithe 2012
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  9. 9
    Transcriptional Consequences of 16p11.2 Deletion and Duplication in Mouse Cortex and Multiplex Autism Families

    Transcriptional Consequences of 16p11.2 Deletion and Duplication in Mouse Cortex and Multiplex Autism Families de réir Ian Blumenthal, Ashok Ragavendran, Serkan Erdin, Lambertus Klei, Aarathi Sugathan, Jolene R. Guide, Poornima Manavalan, Julian Q. Zhou, Vanessa C. Wheeler, Joshua Z. Levin, Carl Ernst, Kathryn Roeder, Bernie Devlin, James F. Gusella, Michael E. Talkowski

    Foilsithe / Cruthaithe 2014
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  10. 10
    How rare and common risk variation jointly affect liability for autism spectrum disorder

    How rare and common risk variation jointly affect liability for autism spectrum disorder de réir Lambertus Klei, Lora McClain, Behrang Mahjani, Klea Panayidou, Silvia De Rubeis, Anna-Carin Säll Grahnat, Gun Karlsson, Yangyi Lu, Nadine Melhem, Xinyi Xu, Abraham Reichenberg, Sven Sandin, Christina M. Hultman, Joseph D. Buxbaum, Kathryn Roeder, Bernie Devlin

    Foilsithe / Cruthaithe 2021
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  11. 11
    Vitamin D Insufficiency and Severe Asthma Exacerbations in Puerto Rican Children

    Vitamin D Insufficiency and Severe Asthma Exacerbations in Puerto Rican Children de réir John M. Brehm, Edna Acosta‐Pérez, Lambertus Klei, Kathryn Roeder, M. Michael Barmada, Nadia Boutaoui, Erick Forno, Roxanne Kelly, Kathryn Paul, Jody Sylvia, Augusto A. Litonjua, Michael D. Cabana, María Alvarez, Angel Colón‐Semidey, Glorisa Canino, Juan C. Celedón

    Foilsithe / Cruthaithe 2012
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  12. 12
    Most genetic risk for autism resides with common variation

    Most genetic risk for autism resides with common variation de réir Trent Gaugler, Lambertus Klei, Stephan Sanders, Corneliu Bodea, Arthur P. Goldberg, Ann B. Lee, Milind Mahajan, Dina Manaa, Yudi Pawitan, Jennifer Reichert, Stephan Ripke, Sven Sandin, Pamela Sklar, Oscar Svantesson, Abraham Reichenberg, Christina M. Hultman, Bernie Devlin, Kathryn Roeder, Joseph D. Buxbaum

    Foilsithe / Cruthaithe 2014
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  13. 13
    High-Density Association Study of 383 Candidate Genes for Volumetric BMD at the Femoral Neck and Lumbar Spine Among Older Men

    High-Density Association Study of 383 Candidate Genes for Volumetric BMD at the Femoral Neck and Lumbar Spine Among Older Men de réir Laura M Yerges, Lambertus Klei, Jane A. Cauley, Kathryn Roeder, Candace M. Kammerer, Susan P Moffett, Kristine E. Ensrud, Cara S. Nestlerode, Lynn M. Marshall, Andrew R. Hoffman, Cora E. Lewis, Thomas Lang, Elizabeth Barrett‐Connor, Robert E. Ferrell, Eric Orwoll, Joseph M. Zmuda

    Foilsithe / Cruthaithe 2009
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  14. 14
    The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment

    The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment de réir Justin Cotney, Rebecca Muhle, Stephan Sanders, Li Liu, A. Jeremy Willsey, Wei Niu, Wenzhong Liu, Lambertus Klei, Jing Lei, Jun Yin, Steven K. Reilly, Andrew T.N. Tebbenkamp, Candace Bichsel, Mihovil Pletikos, Nenad Šestan, Kathryn Roeder, Matthew W. State, Bernie Devlin, James P. Noonan

    Foilsithe / Cruthaithe 2015
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  15. 15
    DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics

    DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics de réir Li Liu, Jing Lei, Stephan Sanders, A. Jeremy Willsey, Yan Kou, A. Ercüment Çiçek, Lambertus Klei, Cong Lu, Xin He, Mingfeng Li, Rebecca Muhle, Avi Ma’ayan, James P. Noonan, Nenad Šestan, Kathryn McFadden, Matthew W. State, Joseph D. Buxbaum, Bernie Devlin, Kathryn Roeder

    Foilsithe / Cruthaithe 2014
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  16. 16
    African ancestry and lung function in Puerto Rican children

    African ancestry and lung function in Puerto Rican children de réir John M. Brehm, Edna Acosta‐Pérez, Lambertus Klei, Kathryn Roeder, M. Michael Barmada, Nadia Boutaoui, Erick Forno, Michelle M. Cloutier, Soma Datta, Roxanne Kelly, Kathryn Paul, Jody Sylvia, Deanna Calvert, Sherell Thornton‐Thompson, Dorothy Wakefield, Augusto A. Litonjua, María Alvarez, Angel Colón‐Semidey, Glorisa Canino, Juan C. Celedón

    Foilsithe / Cruthaithe 2012
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  17. 17
    Genetic risk for schizophrenia and psychosis in Alzheimer disease

    Genetic risk for schizophrenia and psychosis in Alzheimer disease de réir Mary Ann A. DeMichele‐Sweet, Elise A. Weamer, Lambertus Klei, Dylan T. Vrana, Deborah Hollingshead, Howard Seltman, Rebecca Sims, Tatiana Foroud, Isabel Hernández, Sonia Moreno‐Grau, Lluís Tárraga, Merçé Boada, Agustı́n Ruiz, Julie Williams, Richard Mayeux, Oscar L. López, Etienne Sibille, M. Ilyas Kamboh, Bernie Devlin, Robert A. Sweet

    Foilsithe / Cruthaithe 2017
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  18. 18
    Consanguinity and increased risk for schizophrenia in Egypt

    Consanguinity and increased risk for schizophrenia in Egypt de réir Hader Mansour, Warda Fathi, Lambertus Klei, Joel Wood, Kodavali V. Chowdari, Annie Watson, Ahmed Eissa, Mai Elassy, ibtihal ali, Hala Salah, Amal Yassin, Salwa Tobar, Hala El‐Boraie, Hanan Gaafar, Nahed E. Ibrahim, Kareem Kandil, Wafaa El‐Bahaei, Osama El‐Boraie, Mohamed Alatrouny, Farha El‐Chennawi, Bernie Devlin, Vishwajit L. Nimgaonkar

    Foilsithe / Cruthaithe 2010
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  19. 19
    Project Among African-Americans to Explore Risks for Schizophrenia (PAARTNERS): Evidence for Impairment and Heritability of Neurocognitive Functioning in Families of Schizophrenia Patients

    Project Among African-Americans to Explore Risks for Schizophrenia (PAARTNERS): Evidence for Impairment and Heritability of Neurocognitive Functioning in Families of Schizophrenia... de réir Monica E. Calkins, Ping G. Tepper, Ruben C. Gur, J. Daniel Ragland, Lambertus Klei, Howard W. Wiener, Jan Richard, Robert Savage, Trina B. Allen, Judith O’Jile, Bernie Devlin, Joseph A. Kwentus, Muktar H. Aliyu, L. DiAnne Bradford, Neil B. Edwards, Paul D. Lyons, Vishwajit L. Nimgaonkar, Alberto B. Santos, Rodney C.P. Go, Raquel E. Gur

    Foilsithe / Cruthaithe 2010
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  20. 20
    A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity?

    A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity? de réir Pauline Chaste, Lambertus Klei, Stephan Sanders, Vanessa Hus, Michael T. Murtha, Jennifer K. Lowe, A. Jeremy Willsey, Daniel Moreno‐De‐Luca, Timothy W. Yu, Éric Fombonne, Daniel H. Geschwind, Dorothy E. Grice, David H. Ledbetter, Shrikant Mane, Donna M. Martin, Eric M. Morrow, Christopher A. Walsh, James S. Sutcliffe, Christa Lese Martin, Arthur L. Beaudet, Catherine Lord, Matthew W. State, Edwin H. Cook, Bernie Devlin

    Foilsithe / Cruthaithe 2014
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