REFINING GENETICALLY INFERRED RELATIONSHIPS USING TREELET COVARIANCE SMOOTHING()

Por Crossett, Andrew, Lee, Ann B., Klei, Lambertus, Devlin, Bernie, Roeder, Kathryn
Publicado em 2012

Discovering Genetic Ancestry Using Spectral Graph Theory

Por Lee, Ann B., Luca, Diana, Klei, Lambertus, Devlin, Bernie, Roeder, Kathryn
Publicado no Genet Epidemiol (2010)

Using ancestry matching to combine family-based and unrelated samples for genome-wide association studies()

Por Crossett, Andrew, Kent, Brian P., Klei, Lambertus, Ringquist, Steven, Trucco, Massimo, Roeder, Kathryn, Devlin, Bernie
Publicado no Stat Med (2010)

No association of psychosis in Alzheimer disease with neurodegenerative pathway genes

Por DeMichele-Sweet, Mary Ann A., Klei, Lambertus, Devlin, Bernie, Ferrell, Robert E., Weamer, Elise A., Emanuel, James E., Lopez, Oscar L., Sweet, Robert A.
Publicado em 2010

On the Use of General Control Samples for Genome-wide Association Studies: Genetic Matching Highlights Causal Variants

Por Luca, Diana, Ringquist, Steven, Klei, Lambertus, Lee, Ann B., Gieger, Christian, Wichmann, H.-Erich, Schreiber, Stefan, Krawczak, Michael, Lu, Ying, Styche, Alexis, Devlin, Bernie, Roeder, Kathryn, Trucco, Massimo
Publicado em 2008

Copy Number Variants for Schizophrenia and Related Psychotic Disorders in Oceanic Palau: Risk and Transmission in Extended Pedigrees

Por Melhem, Nadine, Middleton, Frank, McFadden, Kathryn, Klei, Lambertus, Faraone, Stephen V, Vinogradov, Sophia, Tiobech, Josepha, Yano, Victor, Kuartei, Stevenson, Roeder, Kathryn, Byerley, William, Devlin, Bernie, Myles-Worsley, Marina
Publicado em 2011

Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden

Por Yip, Benjamin Hon Kei, Bai, Dan, Mahjani, Behrang, Klei, Lambertus, Pawitan, Yudi, Hultman, Christina M., Grice, Dorothy E., Roeder, Kathryn, Buxbaum, Joseph D., Devlin, Bernie, Reichenberg, Abraham, Sandin, Sven
Publicado no Biol Psychiatry (2017)

Analysis of Shared Haplotypes amongst Palauans Maps Loci for Psychotic Disorders to 4q28 and 5q23-q31

Por Bodea, Corneliu A., Middleton, Frank A., Melhem, Nadine M., Klei, Lambertus, Song, Youeun, Tiobech, Josepha, Marumoto, Pearl, Yano, Victor, Faraone, Stephen V., Roeder, Kathryn, Myles-Worsley, Marina, Devlin, Bernie, Byerley, William
Publicado no Mol Neuropsychiatry (2017)

Characterizing runs of homozygosity and their impact on risk for psychosis in a population isolate

Por Melhem, Nadine M., Lu, Cong, Dresbold, Cara, Middleton, Frank A., Klei, Lambertus, Wood, Shawn, Faraone, Stephen V, Vinogradov, Sophia, Tiobech, Josepha, Yano, Victor, Roeder, Kathryn, Byerley, William, Myles-Worsley, Marina, Devlin, Bernie
Publicado no Am J Med Genet B Neuropsychiatr Genet (2014)

Genome-wide Transcriptome Profiling Reveals the Functional Impact of Rare De Novo and Recurrent CNVs in Autism Spectrum Disorders

Por Luo, Rui, Sanders, Stephan J., Tian, Yuan, Voineagu, Irina, Huang, Ni, Chu, Su H., Klei, Lambertus, Cai, Chaochao, Ou, Jing, Lowe, Jennifer K., Hurles, Matthew E., Devlin, Bernie, State, Matthew W., Geschwind, Daniel H.
Publicado em 2012

Runs of Homozygosity, Copy Number Variation, and Risk for Depression and Suicidal Behavior in an Arab Bedouin Kindred

Por Melhem, Nadine M., Hamdan, Sami, Klei, Lambertus, Wood, Shawn, Zelazny, Jamie, Frisch, Amos, Weizman, Abraham, Carmel, Miri, Michaelovsky, Elena, Farbstein, Ilana, Wasserman, Danuta, el Heib, Muhammad, Ferrell, Robert, Apter, Alan, Devlin, Bernie, Brent, David
Publicado no Psychiatr Genet (2017)

Transcriptional Consequences of 16p11.2 Deletion and Duplication in Mouse Cortex and Multiplex Autism Families

Por Blumenthal, Ian, Ragavendran, Ashok, Erdin, Serkan, Klei, Lambertus, Sugathan, Aarathi, Guide, Jolene R., Manavalan, Poornima, Zhou, Julian Q., Wheeler, Vanessa C., Levin, Joshua Z., Ernst, Carl, Roeder, Kathryn, Devlin, Bernie, Gusella, James F., Talkowski, Michael E.
Publicado em 2014

Vitamin D Insufficiency and Severe Asthma Exacerbations in Puerto Rican Children

Por Brehm, John M., Acosta-Pérez, Edna, Klei, Lambertus, Roeder, Kathryn, Barmada, Michael, Boutaoui, Nadia, Forno, Erick, Kelly, Roxanne, Paul, Kathryn, Sylvia, Jody, Litonjua, Augusto A., Cabana, Michael, Alvarez, María, Colón-Semidey, Angel, Canino, Glorisa, Celedón, Juan C.
Publicado em 2012

Principal Components of Heritability From Neurocognitive Domains Differ Between Families With Schizophrenia and Control Subjects

Por Wiener, Howard, Klei, Lambertus, Calkins, Monica, Wood, Joel, Nimgaonkar, Vishwajit, Gur, Ruben, Bradford, L. DiAnne, Richard, Jan, Edwards, Neil, Savage, Robert, Kwentus, Joseph, Allen, Trina, McEvoy, Joseph, Santos, Alberto, Gur, Raquel, Devlin, Bernie, Go, Rodney
Publicado em 2013

Amino Acid Position 11 of HLA-DRβ1 is a Major Determinant of Chromosome 6p Association with Ulcerative Colitis

Por Achkar, Jean-Paul, Klei, Lambertus, de Bakker, Paul I.W., Bellone, Gaia, Rebert, Nancy, Scott, Regan, Lu, Ying, Regueiro, Miguel, Brzezinski, Aaron, Kamboh, M. Ilyas, Fiocchi, Claudio, Devlin, Bernie, Trucco, Massimo, Ringquist, Steven, Roeder, Kathryn, Duerr, Richard H
Publicado em 2011

Candidate Gene Analysis of Femoral Neck Trabecular and Cortical Volumetric Bone Mineral Density in Older Men

Por Yerges, Laura M, Klei, Lambertus, Cauley, Jane A, Roeder, Kathryn, Kammerer, Candace M, Ensrud, Kristine E, Nestlerode, Cara S, Lewis, Cora, Lang, Thomas F, Barrett-Connor, Elizabeth, Moffett, Susan P, Hoffman, Andrew R, Ferrell, Robert E, Orwoll, Eric S, Zmuda, Joseph M
Publicado em 2010

High-Density Association Study of 383 Candidate Genes for Volumetric BMD at the Femoral Neck and Lumbar Spine Among Older Men

Por Yerges, Laura M., Klei, Lambertus, Cauley, Jane A., Roeder, Kathryn, Kammerer, Candace M., Moffett, Susan P., Ensrud, Kristine E., Nestlerode, Cara S., Marshall, Lynn M., Hoffman, Andrew R., Lewis, Cora, Lang, Thomas F., Barrett-Connor, Elizabeth, Ferrell, Robert E., Orwoll, Eric S., Zmuda, Joseph M.
Publicado em 2009

Genetic Analysis of Vertebral Trabecular Bone Density and Cross-Sectional Area in Older Men

Por Zmuda, Joseph M., Yerges-Armstrong, Laura M., Moffett, Susan P., Klei, Lambertus, Kammerer, Candace M., Roeder, Kathryn, Cauley, Jane A., Kuipers, Allison, Ensrud, Kristine E., Nestlerode, Cara S., Hoffman, Andrew R., Lewis, Cora E., Lang, Thomas F., Barrett-Connor, Elizabeth, Ferrell, Robert E., Orwoll, Eric S.
Publicado em 2010

Most genetic risk for autism resides with common variation

Por Gaugler, Trent, Klei, Lambertus, Sanders, Stephan J., Bodea, Corneliu A., Goldberg, Arthur P., Lee, Ann B., Mahajan, Milind, Manaa, Dina, Pawitan, Yudi, Reichert, Jennifer, Ripke, Stephan, Sandin, Sven, Sklar, Pamela, Svantesson, Oscar, Reichenberg, Abraham, Hultman, Christina M., Devlin, Bernie, Roeder, Kathryn, Buxbaum, Joseph D.
Publicado em 2014

The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment

Por Cotney, Justin, Muhle, Rebecca A., Sanders, Stephan J., Liu, Li, Willsey, A. Jeremy, Niu, Wei, Liu, Wenzhong, Klei, Lambertus, Lei, Jing, Yin, Jun, Reilly, Steven K., Tebbenkamp, Andrew T., Bichsel, Candace, Pletikos, Mihovil, Sestan, Nenad, Roeder, Kathryn, State, Matthew W., Devlin, Bernie, Noonan, James P.
Publicado no Nat Commun (2015)