Reinhold E Schmidt
Genetic variants for head size share genes and pathways with cancer.
Knol M, Poot R, Evans T, Satizabal C, Mishra A, Sargurupremraj M, van der Auwera S, Duperron M, Jian X, Hostettler I, van Dam-Nolen D, Lamballais S, Pawlak M, Lewis C, Carrion-Castillo A, van Erp T, Reinbold C, Shin J, Scholz M, Håberg A, Kämpe A, Li G, Avinun R, Atkins J, Hsu F, Amod A, Lam M, Tsuchida A, Teunissen M, Aygün N, Patel Y, Liang D, Beiser A, Beyer F, Bis J, Bos D, Bryan R, Bülow R, Caspers S, Catheline G, Cecil C, Dalvie S, Dartigues J, DeCarli C, Enlund-Cerullo M, Ford J, Franke B, Freedman B, Friedrich N, Green M, Haworth S, Helmer C, Hoffmann P, Homuth G, Ikram M, Jack C, Jahanshad N, Jockwitz C, Kamatani Y, Knodt A, Li S, Lim K, Longstreth W, Macciardi F, Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium, Enhancing NeuroImaging Genetics through Meta-Analysis (ENIGMA) Consortium, Mäkitie O, Mazoyer B, Medland S, Miyamoto S, Moebus S, Mosley T, Muetzel R, Mühleisen T, Nagata M, Nakahara S, Palmer N, Pausova Z, Preda A, Quidé Y, Reay W, Roshchupkin G, Schmidt R, Schreiner P, Setoh K, Shapland C, Sidney S, St Pourcain B, Stein J, Tabara Y, Teumer A, Uhlmann A, van der Lugt A, Vernooij M, Werring D, Windham B, Witte A, Wittfeld K, Yang Q, Yoshida K, Brunner H, Le Grand Q, Sim K, Stein D, Bowden D, Cairns M, Hariri A, Cheung C, Andersson S, Villringer A, Paus T, Cichon S, Calhoun V, Crivello F, Launer L, White T, Koudstaal P, Houlden H, Fornage M, Matsuda F, Grabe H, Debette S, Thompson P, Seshadri S, Adams H. Genetic variants for head size share genes and pathways with cancer. Cell Rep Med 2024:101529.
May 3, 2024Genetic variants for head size share genes and pathways with cancer.
May 3, 2024Cell Rep Med 2024:101529
Knol Maria J, Poot Raymond A, Evans Tavia E, Satizabal Claudia L, Mishra Aniket, Sargurupremraj Muralidharan, van der Auwera Sandra, Duperron Marie-Gabrielle, Jian Xueqiu, Hostettler Isabel, van Dam-Nolen Dianne H K, Lamballais Sander, Pawlak Mikolaj A, Lewis Cora E, Carrion-Castillo Amaia, van Erp Theo G M, Reinbold Céline S, Shin Jean, Scholz Markus, Håberg Asta K, Kämpe Anders, Li Gloria H Y, Avinun Reut, Atkins Joshua R, Hsu Fang-Chi, Amod AlyR, Lam Max, Tsuchida Ami, Teunissen Mariël W A, Aygün Nil, Patel Yash, Liang Dan, Beiser Alexa S, Beyer Frauke, Bis Joshua C, Bos Daniel, Bryan R Nick, Bülow Robin, Caspers Svenja, Catheline Gwenaëlle, Cecil Charlotte A M, Dalvie Shareefa, Dartigues Jean-François, DeCarli Charles, Enlund-Cerullo Maria, Ford Judith M, Franke Barbara, Freedman Barry I, Friedrich Nele, Green MeliJ, Haworth Simon, Helmer Catherine, Hoffmann Per, Homuth Georg, Ikram Mohammad Arfan, Jack Clifford R, Jahanshad Neda, Jockwitz Christiane, Kamatani Yoichiro, Knodt Annchen R, Li Shuo, Lim Keane, Longstreth W T, Macciardi Fabio, Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium, Enhancing NeuroImaging Genetics through Meta-Analysis (ENIGMA) Consortium, Mäkitie Outi, Mazoyer Bernard, Medland Sarah E, Miyamoto Susumu, Moebus Susanne, Mosley Thomas H, Muetzel Ryan, Mühleisen Thomas W, Nagata Manabu, Nakahara Soichiro, Palmer Nicholette D, Pausova Zdenka, Preda Adrian, Quidé Yann, Reay William R, Roshchupkin Gennady V, Schmidt Reinhold E, Schreiner Pamela J, Setoh Kazuya, Shapland Chin Yang, Sidney Stephen, St Pourcain Beate, Stein Jason L, Tabara Yasuharu, Teumer Alexander, Uhlmann Anne, van der Lugt Aad, Vernooij Meike W, Werring David J, Windham B Gwen, Witte A Veronica, Wittfeld Katharina, Yang Qiong, Yoshida Kazumichi, Brunner Han G, Le Grand Quentin, Sim Kang, Stein Dan J, Bowden Donald W, Cairns Murray J, Hariri Ahmad R, Cheung Ching-Lung, Andersson Sture, Villringer Arno, Paus Tomas, Cichon Sven, Calhoun Vince D, Crivello Fabrice, Launer Lenore J, White Tonya, Koudstaal Peter J, Houlden Henry, Fornage Myriam, Matsuda Fumihiko, Grabe Hans Jörgen, Debette Stephanie, Thompson Paul M, Seshadri Sudha, Adams Hieab H H
Association of common genetic variants with brain microbleeds: A genome-wide association study.
MacKinnon A, Gottesman R, Schmidt R, Houlden H, Stott D, Koh J, Beekman M, Amin N, Vernooij M, Tozer D, Beiser A, Morris Z, Yang Q, Himali J, DeCarli C, Gudnason V, Markus H, Launer L, Seshadri S, Ikram M, Wardlaw J, Schmidt H, Werring D, Mosley T, Jukema J, Rost N, Wong T, Slagboom P, van Duijn C, Deary I, Kantarci K, Pirpamer L, van den Akker E, Hilal S, Giese A, Trompet S, Luciano M, Hostettler I, Liu J, Hofer E, Fornage M, Smith A, Romero J, Adams H, Traylor M, Lu D, Vojinovic D, Li S, Cheng C, Windham B, Bastin M, van der Lugt A, Saba Y, Chen C, van der Grond J, Liewald D, Satizabal C, Yilmaz P, Wilson D, Jack C, van der Lee S, Sigurdsson S, Knol M. Association of common genetic variants with brain microbleeds: A genome-wide association study. Neurology 2020; 95:e3331-e3343.
Sep 10, 2020Association of common genetic variants with brain microbleeds: A genome-wide association study.
Sep 10, 2020Neurology 2020; 95:e3331-e3343
MacKinnon Andrew D, Gottesman Rebecca F, Schmidt Reinhold E, Houlden Henry, Stott David J, Koh Jia Yu, Beekman Marian, Amin Najaf, Vernooij Meike W, Tozer Daniel J, Beiser Alexa S, Morris Zoe, Yang Qiong, Himali Jayandra J, DeCarli Charles, Gudnason Vilmundur, Markus Hugh S, Launer Lenore J, Seshadri Sudha, Ikram M Arfan, Wardlaw Joanna M, Schmidt Helena, Werring David J, Mosley Thomas H, Jukema J Wouter, Rost Natalia S, Wong Tien Yin, Slagboom P Eline, van Duijn Cornelia M, Deary Ian J, Kantarci Kejal, Pirpamer Lukas, van den Akker Erik B, Hilal Saima, Giese Anne-Katrin, Trompet Stella, Luciano Michelle, Hostettler Isabel, Liu Junfeng, Hofer Edith, Fornage Myriam, Smith Albert V, Romero José Rafael J, Adams Hieab H H, Traylor Matthew, Lu Dongwei, Vojinovic Dina, Li Shuo, Cheng Ching Yu, Windham B Gwen, Bastin Mark E, van der Lugt Aad, Saba Yasaman, Chen Christopher, van der Grond Jeroen, Liewald David C M, Satizabal Claudia L, Yilmaz Pinar, Wilson Duncan, Jack Clifford R, van der Lee Sven J, Sigurdsson Sigurdur, Knol Maria J
Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells
Li J, Gieger C, Nöthen M, Büning C, Brand S, Sullivan K, Orange J, Fevang B, Schreiber S, Lieb W, Aukrust P, Chapel H, Cunningham-Rundles C, Franke A, Karlsen T, Grimbacher B, Hakonarson H, Hammarström L, Winkelmann J, Nair R, Elder J, Jørgensen S, Maggadottir S, Bakay M, Warnatz K, Glessner J, Pandey R, Salzer U, Schmidt R, Perez E, Resnick E, Goldacker S, Buchta M, Witte T, Padyukov L, Videm V, Folseraas T, Atschekzei F, Ellinghaus E. Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells. Nat Commun 2015; 6:6804.
Apr 20, 2015Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells
Apr 20, 2015Nat Commun 2015; 6:6804
Li Jin, Gieger Christian, Nöthen Markus M, Büning Carsten, Brand Stephan, Sullivan Kathleen E, Orange Jordan S, Fevang Børre, Schreiber Stefan, Lieb Wolfgang, Aukrust Pål, Chapel Helen, Cunningham-Rundles Charlotte, Franke Andre, Karlsen Tom H, Grimbacher Bodo, Hakonarson Hakon, Hammarström Lennart, Winkelmann Juliane, Nair Rajan P, Elder James T, Jørgensen Silje F, Maggadottir S Melkorka, Bakay Marina, Warnatz Klaus, Glessner Joseph, Pandey Rahul, Salzer Ulrich, Schmidt Reinhold E, Perez Elena, Resnick Elena, Goldacker Sigune, Buchta Mary, Witte Torsten, Padyukov Leonid, Videm Vibeke, Folseraas Trine, Atschekzei Faranaz, Ellinghaus Eva