Depression, Help-Seeking and Self-Recognition of Depression among Dominican, Ecuadorian and Colombian Immigrant Primary Care Patients in the Northeastern United States

por Caplan, Susan, Buyske, Steven
Publicado 2015

TDT-HET: A new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data

por Londono, Douglas, Buyske, Steven, Finch, Stephen J, Sharma, Swarkar, Wise, Carol A, Gordon, Derek
Publicado 2012

Forming Big Datasets through Latent Class Concatenation of Imperfectly Matched Databases Features

por Bartlett, Christopher W., Klamer, Brett G., Buyske, Steven, Petrill, Stephen A., Ray, William C.
Publicado 2019

Increased Expression in Dorsolateral Prefrontal Cortex of CAPON in Schizophrenia and Bipolar Disorder

por Xu, Bin, Wratten, Naomi, Charych, Erik I, Buyske, Steven, Firestein, Bonnie L, Brzustowicz, Linda M
Publicado 2005

Enhanced genetic maps from family-based disease studies: population-specific comparisons

por He, Chunsheng, Weeks, Daniel E, Buyske, Steven, Abecasis, Goncalo R, Stewart, William C, Matise, Tara C
Publicado 2011

Validation of a microRNA target site polymorphism in H3F3B that is potentially associated with a broad schizophrenia phenotype

por Manley, William, Moreau, Michael P., Azaro, Marco, Siecinski, Stephen K., Davis, Gillian, Buyske, Steven, Vieland, Veronica, Bassett, Anne S., Brzustowicz, Linda
Publicado 2018

The Rosetta Phenotype Harmonization Method Facilitates Finding a Relationship Quantitative Trait Locus for a Complex Cognitive Trait

por Petrill, Stephen A., Klamer, Brett G., Buyske, Steven, Willcutt, Erik G., Gruen, Jeffrey R., Francis, David J., Flax, Judy F., Brzustowicz, Linda M., Bartlett, Christopher W.
Publicado 2023

MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders

por Wong, Anthony, Zhou, Anbo, Cao, Xiaolong, Mahaganapathy, Vaidhyanathan, Azaro, Marco, Gwin, Christine, Wilson, Sherri, Buyske, Steven, Bartlett, Christopher W., Flax, Judy F., Brzustowicz, Linda M., Xing, Jinchuan
Publicado 2022

Analysis of case-parent trios at a locus with a deletion allele: association of GSTM1 with autism

por Buyske, Steven, Williams, Tanishia A, Mars, Audrey E, Stenroos, Edward S, Ming, Sue X, Wang, Rong, Sreenath, Madhura, Factura, Marivic F, Reddy, Chitra, Lambert, George H, Johnson, William G
Publicado 2006

Structural Variations Contribute to the Genetic Etiology of Autism Spectrum Disorder and Language Impairments

por Alibutud, Rohan, Hansali, Sammy, Cao, Xiaolong, Zhou, Anbo, Mahaganapathy, Vaidhyanathan, Azaro, Marco, Gwin, Christine, Wilson, Sherri, Buyske, Steven, Bartlett, Christopher W., Flax, Judy F., Brzustowicz, Linda M., Xing, Jinchuan
Publicado 2023

MUSSEL: Enhanced Bayesian Polygenic Risk Prediction Leveraging Information across Multiple Ancestry Groups

por Jin, Jin, Zhan, Jianan, Zhang, Jingning, Zhao, Ruzhang, O’Connell, Jared, Jiang, Yunxuan, Buyske, Steven, Gignoux, Christopher, Haiman, Christopher, Kenny, Eimear E., Kooperberg, Charles, North, Kari, Koelsch, Bertram L., Wojcik, Genevieve, Zhang, Haoyu, Chatterjee, Nilanjan
Publicado 2023

The Next PAGE in Understanding Complex Traits: Design for the Analysis of Population Architecture Using Genetics and Epidemiology (PAGE) Study

por Matise, Tara C., Ambite, Jose Luis, Buyske, Steven, Carlson, Christopher S., Cole, Shelley A., Crawford, Dana C., Haiman, Christopher A., Heiss, Gerardo, Kooperberg, Charles, Marchand, Loic Le, Manolio, Teri A., North, Kari E., Peters, Ulrike, Ritchie, Marylyn D., Hindorff, Lucia A., Haines, Jonathan L.
Publicado 2011

Identification of SARS-CoV-2 variants using viral sequencing for the Centers for Disease Control and Prevention genomic surveillance program

por Goswami, Chirayu, Sheldon, Michael, Bixby, Christian, Keddache, Mehdi, Bogdanowicz, Alexander, Wang, Yihe, Schultz, Jonathan, McDevitt, Jessica, LaPorta, James, Kwon, Elaine, Buyske, Steven, Garbolino, Dana, Biloholowski, Glenys, Pastuszak, Alex, Storella, Mary, Bhalla, Amit, Charlier-Rodriguez, Florence, Hager, Russ, Grimwood, Robin, Nahas, Shareef A.
Publicado 2022

Genetic Variation and Reproductive Timing: African American Women from the Population Architecture Using Genomics and Epidemiology (PAGE) Study

por Spencer, Kylee L., Malinowski, Jennifer, Carty, Cara L., Franceschini, Nora, Fernández-Rhodes, Lindsay, Young, Alicia, Cheng, Iona, Ritchie, Marylyn D., Haiman, Christopher A., Wilkens, Lynne, ChunyuanWu, Matise, Tara C., Carlson, Christopher S., Brennan, Kathleen, Park, Amy, Rajkovic, Aleksandar, Hindorff, Lucia A., Buyske, Steven, Crawford, Dana C.
Publicado 2013

Mapping and characterization of structural variation in 17,795 human genomes

por Abel, Haley J., Larson, David E., Regier, Allison A., Chiang, Colby, Das, Indraniel, Kanchi, Krishna L., Layer, Ryan M., Neale, Benjamin M., Salerno, William J., Reeves, Catherine, Buyske, Steven, Matise, Tara C., Muzny, Donna M., Zody, Michael C., Lander, Eric S., Dutcher, Susan K., Stitziel, Nathan O., Hall, Ira M.
Publicado 2020

FAVOR: functional annotation of variants online resource and annotator for variation across the human genome

por Zhou, Hufeng, Arapoglou, Theodore, Li, Xihao, Li, Zilin, Zheng, Xiuwen, Moore, Jill, Asok, Abhijith, Kumar, Sushant, Blue, Elizabeth E, Buyske, Steven, Cox, Nancy, Felsenfeld, Adam, Gerstein, Mark, Kenny, Eimear, Li, Bingshan, Matise, Tara, Philippakis, Anthony, Rehm, Heidi L, Sofia, Heidi J, Snyder, Grace, Weng, Zhiping, Neale, Benjamin, Sunyaev, Shamil R, Lin, Xihong
Publicado 2022

Fine-Mapping and Initial Characterization of QT Interval Loci in African Americans

por Avery, Christy L., Sethupathy, Praveen, Buyske, Steven, He, Qianchuan, Lin, Dan-Yu, Arking, Dan E., Carty, Cara L., Duggan, David, Fesinmeyer, Megan D., Hindorff, Lucia A., Jeff, Janina M., Klein, Liviu, Patton, Kristen K., Peters, Ulrike, Shohet, Ralph V., Sotoodehnia, Nona, Young, Alicia M., Kooperberg, Charles, Haiman, Christopher A., Mohlke, Karen L., Whitsel, Eric A., North, Kari E.
Publicado 2012

Generalization and Dilution of Association Results from European GWAS in Populations of Non-European Ancestry: The PAGE Study

por Carlson, Christopher S., Matise, Tara C., North, Kari E., Haiman, Christopher A., Fesinmeyer, Megan D., Buyske, Steven, Schumacher, Fredrick R., Peters, Ulrike, Franceschini, Nora, Ritchie, Marylyn D., Duggan, David J., Spencer, Kylee L., Dumitrescu, Logan, Eaton, Charles B., Thomas, Fridtjof, Young, Alicia, Carty, Cara, Heiss, Gerardo, Le Marchand, Loic, Crawford, Dana C., Hindorff, Lucia A., Kooperberg, Charles L.
Publicado 2013

Genetics of Chronic Kidney Disease Stages Across Ancestries: The PAGE Study

por Lin, Bridget M., Nadkarni, Girish N., Tao, Ran, Graff, Mariaelisa, Fornage, Myriam, Buyske, Steven, Matise, Tara C., Highland, Heather M., Wilkens, Lynne R., Carlson, Christopher S., Park, S. Lani, Setiawan, V. Wendy, Ambite, Jose Luis, Heiss, Gerardo, Boerwinkle, Eric, Lin, Dan-Yu, Morris, Andrew P., Loos, Ruth J. F., Kooperberg, Charles, North, Kari E., Wassel, Christina L., Franceschini, Nora
Publicado 2019

Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans

por Franceschini, Nora, Carty, Cara L., Lu, Yingchang, Tao, Ran, Sung, Yun Ju, Manichaikul, Ani, Haessler, Jeff, Fornage, Myriam, Schwander, Karen, Zubair, Niha, Bien, Stephanie, Hindorff, Lucia A., Guo, Xiuqing, Bielinski, Suzette J., Ehret, Georg, Kaufman, Joel D., Rich, Stephen S., Carlson, Christopher S., Bottinger, Erwin P., North, Kari E., Rao, D. C., Chakravarti, Aravinda, Barrett, Paula Q., Loos, Ruth J. F., Buyske, Steven, Kooperberg, Charles
Publicado 2016