Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Liam Cotter"'
Autor:
Noam D. Beckmann, Phillip H. Comella, Esther Cheng, Lauren Lepow, Aviva G. Beckmann, Scott R. Tyler, Konstantinos Mouskas, Nicole W. Simons, Gabriel E. Hoffman, Nancy J. Francoeur, Diane Marie Del Valle, Gurpawan Kang, Anh Do, Emily Moya, Lillian Wilkins, Jessica Le Berichel, Christie Chang, Robert Marvin, Sharlene Calorossi, Alona Lansky, Laura Walker, Nancy Yi, Alex Yu, Jonathan Chung, Matthew Hartnett, Melody Eaton, Sandra Hatem, Hajra Jamal, Alara Akyatan, Alexandra Tabachnikova, Lora E. Liharska, Liam Cotter, Brian Fennessy, Akhil Vaid, Guillermo Barturen, Hardik Shah, Ying-chih Wang, Shwetha Hara Sridhar, Juan Soto, Swaroop Bose, Kent Madrid, Ethan Ellis, Elyze Merzier, Konstantinos Vlachos, Nataly Fishman, Manying Tin, Melissa Smith, Hui Xie, Manishkumar Patel, Kai Nie, Kimberly Argueta, Jocelyn Harris, Neha Karekar, Craig Batchelor, Jose Lacunza, Mahlet Yishak, Kevin Tuballes, Ieisha Scott, Arvind Kumar, Suraj Jaladanki, Charuta Agashe, Ryan Thompson, Evan Clark, Bojan Losic, Lauren Peters, The Mount Sinai COVID-19 Biobank Team, Panagiotis Roussos, Jun Zhu, Wenhui Wang, Andrew Kasarskis, Benjamin S. Glicksberg, Girish Nadkarni, Dusan Bogunovic, Cordelia Elaiho, Sandeep Gangadharan, George Ofori-Amanfo, Kasey Alesso-Carra, Kenan Onel, Karen M. Wilson, Carmen Argmann, Supinda Bunyavanich, Marta E. Alarcón-Riquelme, Thomas U. Marron, Adeeb Rahman, Seunghee Kim-Schulze, Sacha Gnjatic, Bruce D. Gelb, Miriam Merad, Robert Sebra, Eric E. Schadt, Alexander W. Charney
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-15 (2021)
Multisystem inflammatory syndrome in children (MIS-C) onsets in COVID-19 patients with manifestations similar to Kawasaki disease (KD). Here the author probe the peripheral blood transcriptome of MIS-C patients to find signatures related to natural k
Externí odkaz:
https://doaj.org/article/7233a40d610f443eac2e6011b12c9368
Autor:
Jessica S, Johnson, Alanna C, Cote, Amanda, Dobbyn, Laura G, Sloofman, Jiayi, Xu, Liam, Cotter, Alexander W, Charney, Andreas, Birgegård, Jennifer, Jordan, Martin, Kennedy, Mikaél, Landén, Sarah L, Maguire, Nicholas G, Martin, Preben Bo, Mortensen, Laura M, Thornton, Cynthia M, Bulik, Laura M, Huckins
Publikováno v:
Johnson, J S, Cote, A C, Dobbyn, A, Sloofman, L G, Xu, J, Cotter, L, Charney, A W, Birgegård, A, Jordan, J, Kennedy, M, Landén, M, Maguire, S L, Martin, N G, Mortensen, P B, Thornton, L M, Bulik, C M, Huckins, L M & Eating Disorders Working Group of the Psychiatric Genomics Consortium 2023, ' Mapping anorexia nervosa genes to clinical phenotypes ', Psychological Medicine, vol. 53, no. 6, pp. 2629-2633 . https://doi.org/10.1017/S0033291721004554
BackgroundAnorexia nervosa (AN) is a psychiatric disorder with complex etiology, with a significant portion of disease risk imparted by genetics. Traditional genome-wide association studies (GWAS) produce principal evidence for the association of gen
Autor:
Paul F. O'Reilly, Steven A. McCarroll, Mark Hyman Rapaport, Noam D. Beckmann, Eric D. Achtyes, Dolores Malaspina, Ruth J. F. Loos, Michele T. Pato, Gillian M. Belbin, Liam Cotter, Alexander W. Charney, Michael Preuss, Carlos N. Pato, Benjamin S. Glicksberg, Ayman H. Fanous, Deepak Kaji, Eimear E. Kenny, Peter F. Buckley, Douglas S. Lehrer, Tim B. Bigdeli, Tielman Van Vleck, Isotta Landi, Girish N. Nadkarni, Eric E. Schadt
Publikováno v:
Nat Med
Polygenic risk scores (PRS) summarize genetic liability to a disease at the individual level, and the aim is to use them as biomarkers of disease and poor outcomes in real-world clinical practice. To date, few studies have assessed the prognostic val
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2eae8938ce13facf89a80f1fb035685
https://europepmc.org/articles/PMC8446329/
https://europepmc.org/articles/PMC8446329/
Autor:
Liam Cotter, Girish N. Nadkarni, Eric D. Achtyes, Noam D. Beckmann, Douglas S. Lehrer, Deepak Kaji, Ayman H. Fanous, Carlos N. Pato, Michael Preuss, Eric E. Schadt, Gillian M. Belbin, Alexander W. Charney, Isotta Landi, Steve McCarroll, Mark Hyman Rapaport, Tim B. Bigdeli, M. T. Pato, Loos R, Van Vleck T, Peter F. Buckley, Dolores Malaspina, Eimear E. Kenny, Benjamin S. Glicksberg
Schizophrenia (SCZ) is the archetypal severe mental illness and one of the most deeply characterized human genetic traits. Like most common diseases SCZ is highly polygenic, and as such its genetic liability can be summarized at the individual level
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3615d5cf462452142e17dd38f5b5717f
https://doi.org/10.1101/2021.03.19.21253906
https://doi.org/10.1101/2021.03.19.21253906
Autor:
Cynthia M. Bulik, Preben Bo Mortensen, Laura G. Sloofman, Laura M. Huckins, Alexander W. Charney, Sarah Maguire, Martin A. Kennedy, Mikael Landén, Jennifer Jordan, Liam Cotter, Nicholas G. Martin, Jiayi Xu, Amanda Dobbyn, Alanna C. Cote, Jessica S. Johnson
Anorexia nervosa (AN) is a psychiatric disorder with complex etiology, with a significant portion of disease risk imparted by genetics. Traditional GWAS studies produce principal evidence for the association of genetic variants with disease, and prov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d151507674af6190e01fff7da61aa180
https://doi.org/10.1101/2021.02.12.21250941
https://doi.org/10.1101/2021.02.12.21250941
Autor:
Sandeep Gangadharan, Matthew Harnett, Ryan Thompson, Seunghee Kim-Schulze, Liam Cotter, Melody Eaton, Robert Sebra, Konstantinos Vlachos, Karen M. Wilson, Nicole W. Simons, Jocelyn Harris, Manying Tin, Hardik Shah, Nancy Yi, Scott R. Tyler, Emily Moya, Leisha Scott, Brian Fennessey, Arvind Kumar, Guillermo Barturen, Konstantinos Mouskas, Benjamin S. Glicksberg, Elyze Merzier, Kasey Alesso-Carra, Diane Marie Del Valle, Kevin Tuballes, Alona Lansky, Bojan Losic, Cordelia Elaiho, Yinh-chih Wang, Jessica Le Berichel, Aviva G. Beckmann, Akhil Vaid, Suraj K. Jaladanki, Lora Liharska, Noam D. Beckmann, Hui Xie, Christie Chang, Laura Walker, Mahlet Yishak, Marta E. Alarcón-Riquelme, Evan Clark, Esther Cheng, Bruce D. Gelb, Hajra Jamal, Kent Madrid, Alara Akyatan, Sharlene Calorossi, Carmen Argmann, Craig Batchelor, Kimberly Argueta, Jose Lacunza, Lauren Lepow, Andrew Kasarskis, Gabriel E. Hoffman, Eric E. Schadt, Miriam Merad, Nancy Francoeur, Wenhui Wang, Alexander W. Charney, Sacha Gnjatic, Neha Karekar, Melissa Smith, Sandra Hatem, Thomas U. Marron, Shwetha Hara Sridhar, Ethan Ellis, Kenan Onel, Girish N. Nadkarni, Jun Zhu, Manishkumar Patel, Lillian Wilkins, George Ofori-Amanfo, Swaroop Bose, Robert Marvin, Alex J. Yu, Nataly Fishman, Gurpawan Kang, Phillip H. Comella, Alexandra Tabachnikova, Juan C. Diaz Soto, Adeeb Rahman, Dusan Bogunovic
Publikováno v:
medRxiv
article-version (status) pre
article-version (number) 1
Nature Communications
article-version (status) pre
article-version (number) 1
Nature Communications
Multisystem inflammatory syndrome in children (MIS-C) presents with fever, inflammation and pathology of multiple organs in individuals under 21 years of age in the weeks following severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infectio