Polygenic analyses show important differences between MDD symptoms collected using PHQ9 and CIDI-SF

por Huang, Lianyun, Tang, Sonja, Rietkerk, Jolien, Appadurai, Vivek, Krebs, Morten Dybdahl, Schork, Andrew J., Werge, Thomas, Zuber, Verena, Kendler, Kenneth, Cai, Na
Publicado 2023

A comprehensive map of genetic relationships among diagnostic categories based on 48.6 million relative pairs from the Danish genealogy

por Athanasiadis, Georgios, Meijsen, Joeri J., Helenius, Dorte, Schork, Andrew J., Ingason, Andrés, Thompson, Wesley K., Geschwind, Daniel H., Werge, Thomas, Buil, Alfonso
Publicado 2022

An Empirical Bayes Mixture Model for Effect Size Distributions in Genome-Wide Association Studies

por Thompson, Wesley K., Wang, Yunpeng, Schork, Andrew J., Witoelar, Aree, Zuber, Verena, Xu, Shujing, Werge, Thomas, Holland, Dominic, Andreassen, Ole A., Dale, Anders M.
Publicado 2015

Circulating S100B levels at birth and risk of six major neuropsychiatric or neurological disorders: a two-sample Mendelian Randomization Study

por Pan, Mengyu, Roe, James M., Nudel, Ron, Schork, Andrew J., Iakunchykova, Olena, Fjell, Anders M., Walhovd, Kristine B., Werge, Thomas, Chen, Chi-hua, Benros, Michael E., Wang, Yunpeng
Publicado 2023

MicroRNAs enrichment in GWAS of complex human phenotypes

por Goulart, Luiz F, Bettella, Francesco, Sønderby, Ida E, Schork, Andrew J, Thompson, Wesley K, Mattingsdal, Morten, Steen, Vidar M, Zuber, Verena, Wang, Yunpeng, Dale, Anders M, Andreassen, Ole A, Djurovic, Srdjan
Publicado 2015

Probing the Association between Early Evolutionary Markers and Schizophrenia

por Srinivasan, Saurabh, Bettella, Francesco, Hassani, Sahar, Wang, Yunpeng, Witoelar, Aree, Schork, Andrew J., Thompson, Wesley K., Collier, David A., Desikan, Rahul S., Melle, Ingrid, Dale, Anders M., Djurovic, Srdjan, Andreassen, Ole A.
Publicado 2017

All SNPs Are Not Created Equal: Genome-Wide Association Studies Reveal a Consistent Pattern of Enrichment among Functionally Annotated SNPs

por Schork, Andrew J., Thompson, Wesley K., Pham, Phillip, Torkamani, Ali, Roddey, J. Cooper, Sullivan, Patrick F., Kelsoe, John R., O'Donovan, Michael C., Furberg, Helena, Schork, Nicholas J., Andreassen, Ole A., Dale, Anders M.
Publicado 2013

Accuracy of haplotype estimation and whole genome imputation affects complex trait analyses in complex biobanks

por Appadurai, Vivek, Bybjerg-Grauholm, Jonas, Krebs, Morten Dybdahl, Rosengren, Anders, Buil, Alfonso, Ingason, Andrés, Mors, Ole, Børglum, Anders D., Hougaard, David M., Nordentoft, Merete, Mortensen, Preben B., Delaneau, Olivier, Werge, Thomas, Schork, Andrew J.
Publicado 2023

Spatial fine-mapping for gene-by-environment effects identifies risk hot spots for schizophrenia

por Fan, Chun Chieh, McGrath, John J., Appadurai, Vivek, Buil, Alfonso, Gandal, Michael J., Schork, Andrew J., Mortensen, Preben Bo, Agerbo, Esben, Geschwind, Sandy A., Geschwind, Daniel, Werge, Thomas, Thompson, Wesley K., Pedersen, Carsten Bøcker
Publicado 2018

A large population-based investigation into the genetics of susceptibility to gastrointestinal infections and the link between gastrointestinal infections and mental illness

por Nudel, Ron, Appadurai, Vivek, Schork, Andrew J., Buil, Alfonso, Bybjerg-Grauholm, Jonas, Børglum, Anders D., Daly, Mark J., Mors, Ole, Hougaard, David M., Mortensen, Preben Bo, Werge, Thomas, Nordentoft, Merete, Thompson, Wesley K., Benros, Michael E.
Publicado 2020

Genetic Sharing with Cardiovascular Disease Risk Factors and Diabetes Reveals Novel Bone Mineral Density Loci

por Reppe, Sjur, Wang, Yunpeng, Thompson, Wesley K., McEvoy, Linda K., Schork, Andrew J., Zuber, Verena, LeBlanc, Marissa, Bettella, Francesco, Mills, Ian G., Desikan, Rahul S., Djurovic, Srdjan, Gautvik, Kaare M., Dale, Anders M., Andreassen, Ole A.
Publicado 2015

Associations between patterns in comorbid diagnostic trajectories of individuals with schizophrenia and etiological factors

por Krebs, Morten Dybdahl, Themudo, Gonçalo Espregueira, Benros, Michael Eriksen, Mors, Ole, Børglum, Anders D., Hougaard, David, Mortensen, Preben Bo, Nordentoft, Merete, Gandal, Michael J., Fan, Chun Chieh, Geschwind, Daniel H., Schork, Andrew J., Werge, Thomas, Thompson, Wesley K.
Publicado 2021

Enrichment of genetic markers of recent human evolution in educational and cognitive traits

por Srinivasan, Saurabh, Bettella, Francesco, Frei, Oleksandr, Hill, W. David, Wang, Yunpeng, Witoelar, Aree, Schork, Andrew J., Thompson, Wesley K., Davies, Gail, Desikan, Rahul S., Deary, Ian J., Melle, Ingrid, Ueland, Torill, Dale, Anders M., Djurovic, Srdjan, Smeland, Olav B., Andreassen, Ole A.
Publicado 2018

A new common functional coding variant at the DDC gene change renal enzyme activity and modify renal dopamine function

por Miramontes-Gonzalez, Jose Pablo, Hightower, Makena, Zhang, Kuixing, Kurosaki, Hiroki, Schork, Andrew J., Biswas, Nilima, Vaingankar, Sucheta, Mahata, Manjula, Lipkowitz, Michael S., Nievergelt, Caroline M., Baker, Dewleen G., Ziegler, Michael G., León-Jiménez, David, González-Sarmiento, Rogelio, Ichinose, Hiroshi, O’Connor, Daniel T.
Publicado 2019

A large-scale genomic investigation of susceptibility to infection and its association with mental disorders in the Danish population

por Nudel, Ron, Wang, Yunpeng, Appadurai, Vivek, Schork, Andrew J., Buil, Alfonso, Agerbo, Esben, Bybjerg-Grauholm, Jonas, Børglum, Anders D., Daly, Mark J., Mors, Ole, Hougaard, David M., Mortensen, Preben B., Werge, Thomas, Nordentoft, Merete, Thompson, Wesley K., Benros, Michael E.
Publicado 2019

ADuLT: An efficient and robust time-to-event GWAS

por Pedersen, Emil M., Agerbo, Esben, Plana-Ripoll, Oleguer, Steinbach, Jette, Krebs, Morten D., Hougaard, David M., Werge, Thomas, Nordentoft, Merete, Børglum, Anders D., Musliner, Katherine L., Ganna, Andrea, Schork, Andrew J., Mortensen, Preben B., McGrath, John J., Privé, Florian, Vilhjálmsson, Bjarni J.
Publicado 2023

Author Correction: A new common functional coding variant at the DDC gene change renal enzyme activity and modify renal dopamine function

por Miramontes-Gonzalez, Jose Pablo, Hightower, C. Makena, Zhang, Kuixing, Kurosaki, Hiroki, Schork, Andrew J., Biswas, Nilima, Vaingankar, Sucheta, Mahata, Manjula, Lipkowitz, Michael S., Nievergelt, Caroline M., Baker, Dewleen G., Ziegler, Michael G., León-Jiménez, David, González-Sarmiento, Rogelio, Ichinose, Hiroshi, O’Connor, Daniel T.
Publicado 2020

Improved Detection of Common Variants Associated with Schizophrenia and Bipolar Disorder Using Pleiotropy-Informed Conditional False Discovery Rate

por Andreassen, Ole A., Thompson, Wesley K., Schork, Andrew J., Ripke, Stephan, Mattingsdal, Morten, Kelsoe, John R., Kendler, Kenneth S., O'Donovan, Michael C., Rujescu, Dan, Werge, Thomas, Sklar, Pamela, Roddey, J. Cooper, Chen, Chi-Hua, McEvoy, Linda, Desikan, Rahul S., Djurovic, Srdjan, Dale, Anders M.
Publicado 2013

Abundant Genetic Overlap between Blood Lipids and Immune-Mediated Diseases Indicates Shared Molecular Genetic Mechanisms

por Andreassen, Ole A., Desikan, Rahul S., Wang, Yunpeng, Thompson, Wesley K., Schork, Andrew J., Zuber, Verena, Doncheva, Nadezhda T., Ellinghaus, Eva, Albrecht, Mario, Mattingsdal, Morten, Franke, Andre, Lie, Benedicte A., Mills, Ian, Aukrust, Pål, McEvoy, Linda K., Djurovic, Srdjan, Karlsen, Tom H., Dale, Anders M.
Publicado 2015

Correction: Abundant Genetic Overlap between Blood Lipids and Immune-Mediated Diseases Indicates Shared Molecular Genetic Mechanisms

por Andreassen, Ole A., Desikan, Rahul S., Wang, Yunpeng, Thompson, Wesley K., Schork, Andrew J., Zuber, Verena, Doncheva, Nadezhda T., Ellinghaus, Eva, Albrecht, Mario, Mattingsdal, Morten, Franke, Andre, Lie, Benedicte A., Mills, Ian G., Aukrust, Pål, McEvoy, Linda K., Djurovic, Srdjan, Karlsen, Tom H., Dale, Anders M.
Publicado 2015