Familial aggregation of tonsillectomy in early childhood and adolescence

por Bager, Peter, Corn, Giulia, Wohlfahrt, Jan, Boyd, Heather A, Feenstra, Bjarke, Melbye, Mads
Publicado 2018

Use of macrolides in mother and child and risk of infantile hypertrophic pyloric stenosis: nationwide cohort study

por Lund, Marie, Pasternak, Björn, Davidsen, Rie B, Feenstra, Bjarke, Krogh, Camilla, Diaz, Lars J, Wohlfahrt, Jan, Melbye, Mads
Publicado 2014

Integrating genetics with newborn metabolomics in infantile hypertrophic pyloric stenosis

por Fadista, João, Skotte, Line, Courraud, Julie, Geller, Frank, Gørtz, Sanne, Wohlfahrt, Jan, Melbye, Mads, Cohen, Arieh S., Feenstra, Bjarke
Publicado 2021

Genetic Variability in Beta-Defensins Is Not Associated with Susceptibility to Staphylococcus aureus Bacteremia

por Fode, Peder, Larsen, Anders Rhod, Feenstra, Bjarke, Jespersgaard, Cathrine, Skov, Robert Leo, Stegger, Marc, Fowler, Vance G., Andersen, Paal Skytt
Publicado 2012

Shared genetic etiology between idiopathic pulmonary fibrosis and COVID-19 severity

por Fadista, João, Kraven, Luke M., Karjalainen, Juha, Andrews, Shea J., Geller, Frank, Baillie, J Kenneth, Wain, Louise V., Jenkins, R.Gisli, Feenstra, Bjarke
Publicado 2021

Association of maternal CNVs in GSTT1/GSTT2 with smoking, preterm delivery, and low birth weight

por Zheng, Xiaojing, Feingold, Eleanor, Ryckman, Kelli K., Shaffer, John R., Boyd, Heather A., Feenstra, Bjarke, Melbye, Mads, Marazita, Mary L., Murray, Jeffrey C., Cuenco, Karen T.
Publicado 2013

Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci

por Fadista, João, Skotte, Line, Karjalainen, Juha, Abner, Erik, Sørensen, Erik, Ullum, Henrik, Werge, Thomas, Esko, Tõnu, Milani, Lili, Palotie, Aarno, Daly, Mark, Melbye, Mads, Feenstra, Bjarke, Geller, Frank
Publicado 2022

Meta-analysis of genome-wide association studies of gestational duration and spontaneous preterm birth identifies new maternal risk loci

por Pasanen, Anu, Karjalainen, Minna K., Zhang, Ge, Tiensuu, Heli, Haapalainen, Antti M., Ojaniemi, Marja, Feenstra, Bjarke, Jacobsson, Bo, Palotie, Aarno, Laivuori, Hannele, Muglia, Louis J., Rämet, Mika, Hallman, Mikko
Publicado 2023

Genetic regulation of gene expression in the epileptic human hippocampus

por Mirza, Nasir, Appleton, Richard, Burn, Sasha, du Plessis, Daniel, Duncan, Roderick, Farah, Jibril Osman, Feenstra, Bjarke, Hviid, Anders, Josan, Vivek, Mohanraj, Rajiv, Shukralla, Arif, Sills, Graeme J., Marson, Anthony G., Pirmohamed, Munir
Publicado 2017

Metabolic Dynamics and Prediction of Gestational Age and Time to Delivery in Pregnant Women

por Liang, Liang, Rasmussen, Marie-Louise Hee, Piening, Brian, Shen, Xiaotao, Chen, Songjie, Röst, Hannes, Snyder, John K., Tibshirani, Robert, Skotte, Line, Lee, Norman CY., Contrepois, Kévin, Feenstra, Bjarke, Zackriah, Hanyah, Snyder, Michael, Melbye, Mads
Publicado 2020

Common variants associated with general and MMR vaccine-related febrile seizures

por Feenstra, Bjarke, Pasternak, Björn, Geller, Frank, Carstensen, Lisbeth, Wang, Tongfei, Huang, Fen, Eitson, Jennifer L., Hollegaard, Mads V., Svanström, Henrik, Vestergaard, Mogens, Hougaard, David M., Schoggins, John W., Jan, Lily Yeh, Melbye, Mads, Hviid, Anders
Publicado 2014

Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis

por Steinthorsdottir, Valgerdur, Thorleifsson, Gudmar, Aradottir, Kristrun, Feenstra, Bjarke, Sigurdsson, Asgeir, Stefansdottir, Lilja, Kristinsdottir, Anna M., Zink, Florian, Halldorsson, Gisli H., Munk Nielsen, Nete, Geller, Frank, Melbye, Mads, Gudbjartsson, Daniel F., Geirsson, Reynir T., Thorsteinsdottir, Unnur, Stefansson, Kari
Publicado 2016

Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis

por Fadista, João, Skotte, Line, Geller, Frank, Bybjerg-Grauholm, Jonas, Gørtz, Sanne, Romitti, Paul A, Caggana, Michele, Kay, Denise M, Matsson, Hans, Boyd, Heather A, Hougaard, David M, Nordenskjöld, Agneta, Mills, James L, Melbye, Mads, Feenstra, Bjarke
Publicado 2019

Study of correlation between the NAT2 phenotype and genotype status among Greenlandic Inuit

por Birch Kristensen, Emilie, Yakimov, Victor, Bjorn-Mortensen, Karen, Soborg, Bolette, Koch, Anders, Andersson, Mikael, Birch Kristensen, Kasper, Michelsen, Sascha Wilk, Skotte, Line, Ahrendt Bjerregaard, Anne, Blaszkewicz, Meinolf, Golka, Klaus, Hengstler, Jan G., Feenstra, Bjarke, Melbye, Mads, Geller, Frank
Publicado 2018

Genetic regulation of spermine oxidase activity and cancer risk: a Mendelian randomization study

por Fadista, João, Yakimov, Victor, Võsa, Urmo, Hansen, Christine S., Kasela, Silva, Skotte, Line, Geller, Frank, Courraud, Julie, Esko, Tõnu, Kukuškina, Viktorija, Buil, Alfonso, Melbye, Mads, Werge, Thomas M., Hougaard, David M., Milani, Lili, Bybjerg-Grauholm, Jonas, Cohen, Arieh S., Feenstra, Bjarke
Publicado 2021

X-Chromosomal Maternal and Fetal SNPs and the Risk of Spontaneous Preterm Delivery in a Danish/Norwegian Genome-Wide Association Study

por Myking, Solveig, Boyd, Heather A., Myhre, Ronny, Feenstra, Bjarke, Jugessur, Astanand, Devold Pay, Aase S., Østensen, Ingrid H. G., Morken, Nils-Halvdan, Busch, Tamara, Ryckman, Kelli K., Geller, Frank, Magnus, Per, Gjessing, Håkon K., Melbye, Mads, Jacobsson, Bo, Murray, Jeffrey C.
Publicado 2013

Acute and persistent symptoms in non-hospitalized PCR-confirmed COVID-19 patients

por Bliddal, Sofie, Banasik, Karina, Pedersen, Ole Birger, Nissen, Janna, Cantwell, Lisa, Schwinn, Michael, Tulstrup, Morten, Westergaard, David, Ullum, Henrik, Brunak, Søren, Tommerup, Niels, Feenstra, Bjarke, Geller, Frank, Ostrowski, Sisse Rye, Grønbæk, Kirsten, Nielsen, Claus Henrik, Nielsen, Susanne Dam, Feldt-Rasmussen, Ulla
Publicado 2021

Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes

por Ruth, Katherine S, Campbell, Purdey J, Chew, Shelby, Lim, Ee Mun, Hadlow, Narelle, Stuckey, Bronwyn GA, Brown, Suzanne J, Feenstra, Bjarke, Joseph, John, Surdulescu, Gabriela L, Zheng, Hou Feng, Richards, J Brent, Murray, Anna, Spector, Tim D, Wilson, Scott G, Perry, John RB
Publicado 2016

Dissecting maternal and fetal genetic effects underlying the associations between maternal phenotypes, birth outcomes, and adult phenotypes: A mendelian-randomization and haplotype...

por Chen, Jing, Bacelis, Jonas, Sole-Navais, Pol, Srivastava, Amit, Juodakis, Julius, Rouse, Amy, Hallman, Mikko, Teramo, Kari, Melbye, Mads, Feenstra, Bjarke, Freathy, Rachel M., Smith, George Davey, Lawlor, Deborah A., Murray, Jeffrey C., Williams, Scott M., Jacobsson, Bo, Muglia, Louis J., Zhang, Ge
Publicado 2020

No Observed Association for Mitochondrial SNPs with Preterm Delivery and Related Outcomes

por Alleman, Brandon W., Myking, Solveig, Ryckman, Kelli K., Myhre, Ronny, Feingold, Eleanor, Feenstra, Bjarke, Geller, Frank, Boyd, Heather A., Shaffer, John R., Zhang, Qi, Begum, Ferdouse, Crosslin, David, Doheny, Kim, Pugh, Elizabeth, Pay, Aase Serine Devold, Østensen, Ingrid H.G., Morken, Nils-Halvdan, Magnus, Per, Marazita, Mary L., Jacobsson, Bo, Melbye, Mads, Murray, Jeffrey C.
Publicado 2012