Henry Houlden
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
Associations of renal function with cerebral small vessel disease and functional outcome in acute intracerebral haemorrhage: A hospital-based prospective cohort study.
Nash P, Best J, Ambler G, Wilson D, Banerjee G, Hostettler I, Seiffge D, Cohen H, Yousry T, Al-Shahi Salman R, Lip G, Brown M, Muir K, Houlden H, Jäger H, Werring D. Associations of renal function with cerebral small vessel disease and functional outcome in acute intracerebral haemorrhage: A hospital-based prospective cohort study. J Neurol Sci 2023; 452:120743.
Jul 28, 2023Associations of renal function with cerebral small vessel disease and functional outcome in acute intracerebral haemorrhage: A hospital-based prospective cohort study.
Jul 28, 2023J Neurol Sci 2023; 452:120743
Nash Philip S, Best Jonathan G, Ambler Gareth, Wilson Duncan, Banerjee Gargi, Hostettler Isabel, Seiffge David Julian, Cohen Hannah, Yousry Tarek A, Al-Shahi Salman Rustam, Lip Gregory Y H, Brown Martin M, Muir Keith, Houlden Henry, Jäger Hans Rolf, Werring David J
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions.
Rahmioglu N, Mortlock S, Ghiasi M, Møller P, Stefansdottir L, Galarneau G, Turman C, Danning R, Law M, Sapkota Y, Christofidou P, Skarp S, Giri A, Banasik K, Krassowski M, Lepamets M, Marciniak B, Nõukas M, Perro D, Sliz E, Sobalska-Kwapis M, Thorleifsson G, Topbas-Selcuki N, Vitonis A, Westergaard D, Arnadottir R, Burgdorf K, Campbell A, Cheuk C, Clementi C, Cook J, De Vivo I, DiVasta A, Dorien O, Donoghue J, Edwards T, Fontanillas P, Fung J, Geirsson R, Girling J, Harkki P, Harris H, Healey M, Heikinheimo O, Holdsworth-Carson S, Hostettler I, Houlden H, Houshdaran S, Irwin J, Jarvelin M, Kamatani Y, Kennedy S, Kepka E, Kettunen J, Kubo M, Kulig B, Kurra V, Laivuori H, Laufer M, Lindgren C, MacGregor S, Mangino M, Martin N, Matalliotaki C, Matalliotakis M, Murray A, Ndungu A, Nezhat C, Olsen C, Opoku-Anane J, Padmanabhan S, Paranjpe M, Peters M, Polak G, Porteous D, Rabban J, Rexrode K, Romanowicz H, Saare M, Saavalainen L, Schork A, Sen S, Shafrir A, Siewierska-Górska A, Słomka M, Smith B, Smolarz B, Szaflik T, Szyłło K, Takahashi A, Terry K, Tomassetti C, Treloar S, Vanhie A, Vincent K, Vo K, Werring D, Zeggini E, Zervou M, DBDS Genomic Consortium, FinnGen Study, FinnGen Endometriosis Taskforce, Celmatix Research Team, 23andMe Research Team, Adachi S, Buring J, Ridker P, D'Hooghe T, Goulielmos G, Hapangama D, Hayward C, Horne A, Low S, Martikainen H, Chasman D, Rogers P, Saunders P, Sirota M, Spector T, Strapagiel D, Tung J, Whiteman D, Giudice L, Velez Edwards D, Uimari O, Kraft P, Salumets A, Nyholt D, Mägi R, Stefansson K, Becker C, Yurttas-Beim P, Steinthorsdottir V, Nyegaard M, Missmer S, Montgomery G, Morris A, Zondervan K. The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. Nat Genet 2023; 55:423-436.
Mar 13, 2023The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions.
Mar 13, 2023Nat Genet 2023; 55:423-436
Rahmioglu Nilufer, Mortlock Sally, Ghiasi Marzieh, Møller Peter L, Stefansdottir Lilja, Galarneau Geneviève, Turman Constance, Danning Rebecca, Law Matthew H, Sapkota Yadav, Christofidou Paraskevi, Skarp Sini, Giri Ayush, Banasik Karina, Krassowski Michal, Lepamets Maarja, Marciniak Błażej, Nõukas Margit, Perro Danielle, Sliz Eeva, Sobalska-Kwapis Marta, Thorleifsson Gudmar, Topbas-Selcuki Nura F, Vitonis Allison, Westergaard David, Arnadottir Ragnheidur, Burgdorf Kristoffer S, Campbell Archie, Cheuk Cecilia S K, Clementi Caterina, Cook James P, De Vivo Immaculata, DiVasta Amy, Dorien O, Donoghue Jacqueline F, Edwards Todd L, Fontanillas Pierre, Fung Jenny N, Geirsson Reynir T, Girling Jane E, Harkki Paivi, Harris Holly R, Healey Martin, Heikinheimo Oskari, Holdsworth-Carson Sarah, Hostettler Isabel, Houlden Henry, Houshdaran Sahar, Irwin Juan C, Jarvelin Marjo-Riitta, Kamatani Yoichiro, Kennedy Stephen H, Kepka Ewa, Kettunen Johannes, Kubo Michiaki, Kulig Bartosz, Kurra Venla, Laivuori Hannele, Laufer Marc R, Lindgren Cecilia M, MacGregor Stuart, Mangino Massimo, Martin Nicholas G, Matalliotaki Charoula, Matalliotakis Michail, Murray Alison D, Ndungu Anne, Nezhat Camran, Olsen Catherine M, Opoku-Anane Jessica, Padmanabhan Sandosh, Paranjpe Manish, Peters Maire, Polak Grzegorz, Porteous David J, Rabban Joseph, Rexrode KathyM, Romanowicz Hanna, Saare Merli, Saavalainen Liisu, Schork Andrew J, Sen Sushmita, Shafrir Amy L, Siewierska-Górska Anna, Słomka Marcin, Smith Blair H, Smolarz Beata, Szaflik Tomasz, Szyłło Krzysztof, Takahashi Atsushi, Terry Kathryn L, Tomassetti Carla, Treloar Susan A, Vanhie Arne, Vincent Katy, Vo Kim C, Werring David J, Zeggini Eleftheria, Zervou Maria I, DBDS Genomic Consortium, FinnGen Study, FinnGen Endometriosis Taskforce, Celmatix Research Team, 23andMe Research Team, Adachi Sosuke, Buring Julie E, Ridker Paul M, D'Hooghe Thomas, Goulielmos George N, Hapangama Dharani K, Hayward Caroline, Horne Andrew W, Low Siew-Kee, Martikainen Hannu, Chasman Daniel I, Rogers Peter A W, Saunders Philippa T, Sirota Marina, Spector Timothy D, Strapagiel Dominik, Tung Joyce Y, Whiteman David C, Giudice Linda C, Velez Edwards Digna R, Uimari Outi, Kraft Peter, Salumets Andres, Nyholt Dale R, Mägi Reedik, Stefansson Kari, Becker Christian M, Yurttas-Beim Piraye, Steinthorsdottir Valgerdur, Nyegaard Mette, Missmer Stacey A, Montgomery Grant W, Morris Andrew P, Zondervan Krina T
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy.
Mingardo E, Beaman G, Grote P, Nordenskjöld A, Newman W, Woolf A, Eckstein M, Hilger A, Dworschak G, Rösch W, Ebert A, Stein R, Brusco A, Di Grazia M, Tamer A, Torres F, Hernandez J, Erben P, Maj C, Olmos J, Riancho J, Valero C, Hostettler I, Houlden H, Werring D, Schumacher J, Gehlen J, Giel A, Buerfent B, Arkani S, Åkesson E, Rotstein E, Ludwig M, Holmdahl G, Giorgio E, Berettini A, Keene D, Cervellione R, Younsi N, Ortlieb M, Oswald J, Haid B, Promm M, Neissner C, Hirsch K, Stehr M, Schäfer F, Schmiedeke E, Boemers T, van Rooij I, Feitz W, Marcelis C, Lacher M, Nelson J, Ure B, Fortmann C, Gale D, Chan M, Ludwig K, Nöthen M, Heilmann S, Zwink N, Jenetzky E, Odermatt B, Knapp M, Reutter H. A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy. Commun Biol 2022; 5:1203.
Nov 9, 2022A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy.
Nov 9, 2022Commun Biol 2022; 5:1203
Mingardo Enrico, Beaman Glenda, Grote Philip, Nordenskjöld Agneta, Newman William, Woolf Adrian S, Eckstein Markus, Hilger Alina C, Dworschak Gabriel C, Rösch Wolfgang, Ebert Anne-Karolin, Stein Raimund, Brusco Alfredo, Di Grazia Massimo, Tamer Ali, Torres Federico M, Hernandez Jose L, Erben Philipp, Maj Carlo, Olmos Jose M, Riancho Jose A, Valero Carmen, Hostettler Isabel C, Houlden Henry, Werring David J, Schumacher Johannes, Gehlen Jan, Giel Ann-Sophie, Buerfent Benedikt C, Arkani Samara, Åkesson Elisabeth, Rotstein Emilia, Ludwig Michael, Holmdahl Gundela, Giorgio Elisa, Berettini Alfredo, Keene David, Cervellione Raimondo M, Younsi Nina, Ortlieb Melissa, Oswald Josef, Haid Bernhard, Promm Martin, Neissner Claudia, Hirsch Karin, Stehr Maximilian, Schäfer Frank-Mattias, Schmiedeke Eberhard, Boemers Thomas M, van Rooij Iris A L M, Feitz Wouter F J, Marcelis Carlo L M, Lacher Martin, Nelson Jana, Ure Benno, Fortmann Caroline, Gale Daniel P, Chan Melanie M Y, Ludwig Kerstin U, Nöthen Markus M, Heilmann Stefanie, Zwink Nadine, Jenetzky Ekkehart, Odermatt Benjamin, Knapp Michael, Reutter Heiko
A Genome-Wide Association Study of Outcome After Aneurysmal Subarachnoid Haemorrhage: Discovery Analysis.
Gaastra B, Alexander S, Bakker M, Bhagat H, Bijlenga P, Blackburn S, Collins M, Doré S, Griessenauer C, Hendrix P, Hong E, Hostettler I, Houlden H, IIhara K, Jeon J, Kim B, Li J, Morel S, Nyquist P, Ren D, Ruigrok Y, Werring D, Tapper W, Galea I, Bulters D. A Genome-Wide Association Study of Outcome After Aneurysmal Subarachnoid Haemorrhage: Discovery Analysis. Transl Stroke Res 2022
Oct 20, 2022A Genome-Wide Association Study of Outcome After Aneurysmal Subarachnoid Haemorrhage: Discovery Analysis.
Oct 20, 2022Transl Stroke Res 2022
Gaastra Ben, Alexander Sheila, Bakker Mark K, Bhagat Hemant, Bijlenga Philippe, Blackburn Spiros, Collins Malie K, Doré Sylvain, Griessenauer Christoph J, Hendrix Philipp, Hong Eun Pyo, Hostettler Isabel C, Houlden Henry, IIhara Koji, Jeon Jin Pyeong, Kim Bong Jun, Li Jiang, Morel Sandrine, Nyquist Paul, Ren Dianxu, Ruigrok Ynte M, Werring David, Tapper Will, Galea Ian, Bulters Diederik
Genetic variation in NFE2L2 is associated with outcome following aneurysmal subarachnoid haemorrhage.
Gaastra B, Duncan P, Bakker M, Hostettler I, Alg V, Houlden H, Ruigrok Y, Galea I, Tapper W, Werring D, Bulters D. Genetic variation in NFE2L2 is associated with outcome following aneurysmal subarachnoid haemorrhage. Eur J Neurol 2022; 30:116-124.
Oct 2, 2022Genetic variation in NFE2L2 is associated with outcome following aneurysmal subarachnoid haemorrhage.
Oct 2, 2022Eur J Neurol 2022; 30:116-124
Gaastra Benjamin, Duncan Poppy, Bakker Mark K, Hostettler Isabel, Alg Varinder S, Houlden Henry, Ruigrok Ynte M, Galea Ian, Tapper Will, Werring David J, Bulters Diederik
Intracranial Aneurysm Classifier Using Phenotypic Factors: An International Pooled Analysis.
Morel S, Hostettler I, Spinner G, Bourcier R, Pera J, Meling T, Alg V, Houlden H, Bakker M, Van't Hof F, Rinkel G, Foroud T, Lai D, Moomaw C, Worrall B, Caroff J, Constant-Dits-Beaufils P, Karakachoff M, Rimbert A, Rouchaud A, Gaal-Paavola E, Kaukovalta H, Kivisaari R, Laakso A, Jahromi B, Tulamo R, Friedrich C, Dauvillier J, Hirsch S, Isidor N, Kulcsàr Z, Lovblad K, Martin O, Machi P, Mendes Pereira V, Rüfenacht D, Schaller K, Schilling S, Slowik A, Jaaskelainen J, von Und Zu Fraunberg M, Jiménez-Conde J, Cuadrado-Godia E, Soriano-Tárraga C, Millwood I, Walters R, The neurIST Project, The Ican Study Group, Genetics And Observational Subarachnoid Haemorrhage Gosh Study Investigators, International Stroke Genetics Consortium Isgc, Kim H, Redon R, Ko N, Rouleau G, Lindgren A, Niemelä M, Desal H, Woo D, Broderick J, Werring D, Ruigrok Y, Bijlenga P. Intracranial Aneurysm Classifier Using Phenotypic Factors: An International Pooled Analysis. J Pers Med 2022; 12
Aug 30, 2022Intracranial Aneurysm Classifier Using Phenotypic Factors: An International Pooled Analysis.
Aug 30, 2022J Pers Med 2022; 12
Morel Sandrine, Hostettler Isabel C, Spinner Georg R, Bourcier Romain, Pera Joanna, Meling Torstein R, Alg Varinder S, Houlden Henry, Bakker Mark K, Van't Hof Femke, Rinkel Gabriel J E, Foroud Tatiana, Lai Dongbing, Moomaw Charles J, Worrall Bradford B, Caroff Jildaz, Constant-Dits-Beaufils Pacôme, Karakachoff Matilde, Rimbert Antoine, Rouchaud Aymeric, Gaal-Paavola Emilia I, Kaukovalta Hanna, Kivisaari Riku, Laakso Aki, Jahromi Behnam Rezai, Tulamo Riikka, Friedrich Christoph M, Dauvillier Jerome, Hirsch Sven, Isidor Nathalie, Kulcsàr Zolt, Lovblad Karl O, Martin Olivier, Machi Paolo, Mendes Pereira Vitor, Rüfenacht Daniel, Schaller Karl, Schilling Sabine, Slowik Agnieszka, Jaaskelainen Juha E, von Und Zu Fraunberg Mikael, Jiménez-Conde Jordi, Cuadrado-Godia Elisa, Soriano-Tárraga Carolina, Millwood Iona Y, Walters Robin G, The neurIST Project, The Ican Study Group, Genetics And Observational Subarachnoid Haemorrhage Gosh Study Investigators, International Stroke Genetics Consortium Isgc, Kim Helen, Redon Richard, Ko NeriU, Rouleau Guy A, Lindgren Antti, Niemelä Mika, Desal Hubert, Woo Daniel, Broderick Joseph P, Werring David J, Ruigrok Ynte M, Bijlenga Philippe
and Cerebral Small Vessel Disease Markers in Patients With Intracerebral Hemorrhage.
Hostettler I, Seiffge D, Wong A, Ambler G, Wilson D, Shakeshaft C, Banerjee G, Sharma N, Jäger H, Cohen H, Yousry T, Al-Shahi Salman R, Lip G, Brown M, Muir K, Houlden H, Werring D. and Cerebral Small Vessel Disease Markers in Patients With Intracerebral Hemorrhage. Neurology 2022; 99:e1290-e1298.
Jul 8, 2022and Cerebral Small Vessel Disease Markers in Patients With Intracerebral Hemorrhage.
Jul 8, 2022Neurology 2022; 99:e1290-e1298
Hostettler Isabel Charlotte, Seiffge David, Wong Andrew, Ambler Gareth, Wilson Duncan, Shakeshaft Clare, Banerjee Gargi, Sharma Nikhil, Jäger Hans Rolf, Cohen Hannah, Yousry Tarek A, Al-Shahi Salman Rustam, Lip Gregory Y H, Brown Martin M, Muir Keith, Houlden Henry, Werring David J
Apolipoprotein E and Cerebral Small Vessel Disease Markers in Patients With Intracerebral Haemorrhage.
Hostettler I, Seiffge D, Wong A, Ambler G, Wilson D, Shakeshaft C, Banerjee G, Sharma N, Jäger H, Cohen H, Yousry T, Al-Shahi Salman R, Lip G, Brown M, Muir K, Houlden H, Werring D. Apolipoprotein E and Cerebral Small Vessel Disease Markers in Patients With Intracerebral Haemorrhage. Neurology 2022
Jul 8, 2022Apolipoprotein E and Cerebral Small Vessel Disease Markers in Patients With Intracerebral Haemorrhage.
Jul 8, 2022Neurology 2022
Hostettler Isabel Charlotte, Seiffge David, Wong Andrew, Ambler Gareth, Wilson Duncan, Shakeshaft Clare, Banerjee Gargi, Sharma Nikhil, Jäger Hans Rudolf, Cohen Hannah, Yousry Tarek A, Al-Shahi Salman Rustam, Lip Gregory Y H, Brown Martin M, Muir Keith, Houlden Henry, Werring David
Magnetic resonance imaging-based scores of small vessel diseases: Associations with intracerebral haemorrhage location.
Schwarz G, Banerjee G, Hostettler I, Ambler G, Seiffge D, Brookes T, Wilson D, Cohen H, Yousry T, Salman R, Lip G, Brown M, Muir K, Houlden H, Jäger R, Werring D, Staals J. Magnetic resonance imaging-based scores of small vessel diseases: Associations with intracerebral haemorrhage location. J Neurol Sci 2022; 434:120165.
Jan 24, 2022Magnetic resonance imaging-based scores of small vessel diseases: Associations with intracerebral haemorrhage location.
Jan 24, 2022J Neurol Sci 2022; 434:120165
Schwarz Ghil, Banerjee Gargi, Hostettler Isabel Charlotte, Ambler Gareth, Seiffge David J, Brookes Tenzin S, Wilson Duncan, Cohen Hannah, Yousry Tarek A, Salman Rustam Al-Shahi, Lip Gregory Y H, Brown Martin M, Muir Keith, Houlden Henry, Jäger Rolf, Werring David J, Staals Julie
MRI and CT imaging biomarkers of cerebral amyloid angiopathy in lobar intracerebral hemorrhage.
Schwarz G, Banerjee G, Hostettler I, Ambler G, Seiffge D, Ozkan H, Browning S, Simister R, Wilson D, Cohen H, Yousry T, Al-Shahi Salman R, Lip G, Brown M, Muir K, Houlden H, Jäger R, Werring D. MRI and CT imaging biomarkers of cerebral amyloid angiopathy in lobar intracerebral hemorrhage. Int J Stroke 2022; 18:85-94.
Jan 7, 2022MRI and CT imaging biomarkers of cerebral amyloid angiopathy in lobar intracerebral hemorrhage.
Jan 7, 2022Int J Stroke 2022; 18:85-94
Schwarz Ghil, Banerjee Gargi, Hostettler Isabel, Ambler Gareth, Seiffge David J, Ozkan Hatice, Browning Simone, Simister Robert J, Wilson Duncan, Cohen Hannah, Yousry Tarek A, Al-Shahi Salman Rustam, Lip Gregory Y H, Brown Martin M, Muir Keith, Houlden Henry, Jäger Rolf, Werring David J
Genome-Wide Association Study of Clinical Outcome After Aneurysmal Subarachnoid Haemorrhage: Protocol.
Gaastra B, Alexander S, Bakker M, Bhagat H, Bijlenga P, Blackburn S, Collins M, Doré S, Griessenauer C, Hendrix P, Hong E, Hostettler I, Houlden H, IIhara K, Jeon J, Kim B, Kumar M, Morel S, Nyquist P, Ren D, Ruigrok Y, Werring D, Galea I, Bulters D, Tapper W. Genome-Wide Association Study of Clinical Outcome After Aneurysmal Subarachnoid Haemorrhage: Protocol. Transl Stroke Res 2022; 13:565-576.
Jan 6, 2022Genome-Wide Association Study of Clinical Outcome After Aneurysmal Subarachnoid Haemorrhage: Protocol.
Jan 6, 2022Transl Stroke Res 2022; 13:565-576
Gaastra Ben, Alexander Sheila, Bakker Mark K, Bhagat Hemant, Bijlenga Philippe, Blackburn Spiros, Collins Malie K, Doré Sylvain, Griessenauer Christoph J, Hendrix Philipp, Hong Eun Pyo, Hostettler Isabel C, Houlden Henry, IIhara Koji, Jeon Jin Pyeong, Kim Bong Jun, Kumar Munish, Morel Sandrine, Nyquist Paul, Ren Dianxu, Ruigrok Ynte M, Werring David, Galea Ian, Bulters Diederik, Tapper Will
Genome-Wide Association Study Identifies Risk Loci for Cluster Headache.
O'Connor E, Danno D, Lagrata S, Grangeon L, Kilbride E, Paemeleire K, Kelderman T, Vikelis M, Cavalleri G, Trembath R, Wood N, Matharu M, Houlden H, Vandrovcova J, Waldenlind E, Sjöstrand C, Steinberg A, Winsvold B, Kockum I, Campbell C, Quinn O, Yip J, Vijfhuizen L, Harder A, Southgate L, Liesecke F, Sivakumar P, Ran C, Fourier C, Giffin N, Silver N, Adebimpe J, Efthymiou S, Sullivan R, Simpson B, Cader M, Davies B, Hostettler I, Ahmed F, Belin A. Genome-Wide Association Study Identifies Risk Loci for Cluster Headache. Ann Neurol 2021; 90:193-202.
Jul 14, 2021Genome-Wide Association Study Identifies Risk Loci for Cluster Headache.
Jul 14, 2021Ann Neurol 2021; 90:193-202
O'Connor Emer, Danno Daisuke, Lagrata Susie, Grangeon Lou, Kilbride Emer, Paemeleire Koen, Kelderman Tim, Vikelis Michail, Cavalleri Gianpiero L, Trembath Richard, Wood Nicholas W, Matharu Manjit, Houlden Henry, Vandrovcova Jana, Waldenlind Elisabet, Sjöstrand Christina, Steinberg Anna, Winsvold Bendik S, Kockum Ingrid, Campbell Ciaran, Quinn Olivia, Yip Janice, Vijfhuizen Lisanne S, Harder Aster V E, Southgate Laura, Liesecke Franziska, Sivakumar Prasanth, Ran Caroline, Fourier Carmen, Giffin Nicola, Silver Nicholas, Adebimpe Joycee, Efthymiou Stephanie, Sullivan Roisin, Simpson Benjamin S, Cader M Zameel, Davies Brendan, Hostettler Isabel, Ahmed Fayyaz, Belin Andrea Carmine
Small vessel disease burden and intracerebral haemorrhage in patients taking oral anticoagulants.
Seiffge D, Jäger H, Muir K, Brown M, Lip G, Al-Shahi Salman R, Yousry T, Cohen H, Shakeshaft C, Houlden H, Hostettler I, Banerjee G, Ambler G, Wilson D, Werring D. Small vessel disease burden and intracerebral haemorrhage in patients taking oral anticoagulants. J Neurol Neurosurg Psychiatry 2021
Mar 19, 2021Small vessel disease burden and intracerebral haemorrhage in patients taking oral anticoagulants.
Mar 19, 2021J Neurol Neurosurg Psychiatry 2021
Seiffge David J, Jäger H, Muir Keith, Brown Martin M, Lip Gregory Y H, Al-Shahi Salman Rustam, Yousry Tarek A, Cohen Hannah, Shakeshaft Clare, Houlden Henry, Hostettler Isabel, Banerjee Gargi, Ambler Gareth, Wilson Duncan, Werring David J
Cerebral Small Vessel Disease and Functional Outcome Prediction After Intracerebral Hemorrhage.
Hostettler I, Schwarz G, Ambler G, Wilson D, Banerjee G, Seiffge D, Shakeshaft C, Lunawat S, Cohen H, Yousry T, Al-Shahi Salman R, Lip G, Brown M, Muir K, Houlden H, Jäger H, Werring D. Cerebral Small Vessel Disease and Functional Outcome Prediction After Intracerebral Hemorrhage. Neurology 2021; 96:e1954-e1965.
Feb 24, 2021Cerebral Small Vessel Disease and Functional Outcome Prediction After Intracerebral Hemorrhage.
Feb 24, 2021Neurology 2021; 96:e1954-e1965
Hostettler Isabel C, Schwarz Ghil, Ambler Gareth, Wilson Duncan, Banerjee Gargi, Seiffge David J, Shakeshaft Clare, Lunawat Surabhika, Cohen Hannah, Yousry Tarek A, Al-Shahi Salman Rustam, Lip Gregory Y H, Brown Martin M, Muir Keith, Houlden Henry, Jäger Hans Rolf, Werring David J
Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.
Ruigrok Y, Sargurupremraj M, Dichgans M, Malik R, Klijn C, Zaroff J, Breen G, Coleman J, Kim H, Ko N, Bown M, Jones G, Martin O, Dauvillier J, Schilling S, Hirsch S, Tatlisumak T, Amouyel P, Debette S, Veldink J, Kamatani Y, Bijlenga P, Redon R, Woo D, Werring D, Broderick J, Lindgren A, von Und Zu Fraunberg M, Jaaskelainen J, Niemelä M, Gaal-Paavola E, Slowik A, Pera J, Worrall B, Rinkel G, Friedrich C, Verschuren W, Zwart J, Chen Z, Millwood I, Liang L, Lin K, Walters R, Matsuda K, Terao C, Akiyama M, Koido M, van Eijk K, Alg V, Hostettler I, Bourcier R, Morel S, van Rheenen W, van der Spek R, Rouleau G, Zhou S, Rannikmäe K, Hveem K, Willer C, Sandvei M, Brumpton B, Johnsen M, Børte S, Winsvold B, Desal H, Eugène F, Shotar E, Gentric J, Naggara O, Dina C, van den Berg L, Houlden H, Sudlow C, Bakker M. Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors. Nat Genet 2021; 53:254.
Feb 1, 2021Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.
Feb 1, 2021Nat Genet 2021; 53:254
Ruigrok Ynte M, Sargurupremraj Muralidharan, Dichgans Martin, Malik Rainer, Klijn Catharina J M, Zaroff Jonathan G, Breen Gerome, Coleman Jonathan R I, Kim Helen, Ko NeriU, Bown Matthew, Jones Gregory T, Martin Olivier, Dauvillier Jerome, Schilling Sabine, Hirsch Sven, Tatlisumak Turgut, Amouyel Philippe, Debette Stephanie, Veldink Jan H, Kamatani Yoichiro, Bijlenga Philippe, Redon Richard, Woo Daniel, Werring David J, Broderick Joseph P, Lindgren Antti, von Und Zu Fraunberg Mikael, Jaaskelainen Juha E, Niemelä Mika, Gaal-Paavola Emilia I, Slowik Agnieszka, Pera Joanna, Worrall Bradford B, Rinkel Gabriel J E, Friedrich Christoph M, Verschuren W M Monique, Zwart John-Anker, Chen Zhengming, Millwood Iona Y, Liang Liming, Lin Kuang, Walters Robin G, Matsuda Koichi, Terao Chikashi, Akiyama Masato, Koido Masaru, van Eijk Kristel R, Alg Varinder S, Hostettler Isabel, Bourcier Romain, Morel Sandrine, van Rheenen Wouter, van der Spek Rick A A, Rouleau Guy A, Zhou Sirui, Rannikmäe Kristiina, Hveem Kristian, Willer Cristen J, Sandvei Marie Søfteland, Brumpton Ben M, Johnsen Marianne Bakke, Børte Sigrid, Winsvold Bendik S, Desal Hubert, Eugène François, Shotar Eimad, Gentric Jean-Christophe, Naggara Olivier, Dina Christian, van den Berg Leonard H, Houlden Henry, Sudlow Cathie L M, Bakker Mark K
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.
Ruigrok Y, Sargurupremraj M, Dichgans M, Malik R, Klijn C, Zaroff J, Breen G, Coleman J, Kim H, Ko N, Bown M, Jones G, Martin O, Dauvillier J, Schilling S, Hirsch S, Tatlisumak T, Amouyel P, Debette S, Veldink J, Kamatani Y, Bijlenga P, Redon R, Woo D, Werring D, Broderick J, Lindgren A, von Und Zu Fraunberg M, Jaaskelainen J, Niemelä M, Gaal-Paavola E, Slowik A, Pera J, Worrall B, Rinkel G, Friedrich C, Verschuren W, Zwart J, Chen Z, Millwood I, Liang L, Lin K, Walters R, Matsuda K, Terao C, Akiyama M, Koido M, van Eijk K, Alg V, Hostettler I, Bourcier R, Morel S, van Rheenen W, van der Spek R, Rouleau G, Zhou S, Rannikmäe K, Hveem K, Willer C, Sandvei M, Brumpton B, Johnsen M, Børte S, Winsvold B, Desal H, Eugène F, Shotar E, Gentric J, Naggara O, Dina C, van den Berg L, Houlden H, Sudlow C, Bakker M. Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors. Nat Genet 2020; 52:1303-1313.
Nov 16, 2020Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.
Nov 16, 2020Nat Genet 2020; 52:1303-1313
Ruigrok Ynte M, Sargurupremraj Muralidharan, Dichgans Martin, Malik Rainer, Klijn Catharina J M, Zaroff Jonathan G, Breen Gerome, Coleman Jonathan R I, Kim Helen, Ko NeriU, Bown Matthew, Jones Gregory T, Martin Olivier, Dauvillier Jerome, Schilling Sabine, Hirsch Sven, Tatlisumak Turgut, Amouyel Philippe, Debette Stephanie, Veldink Jan H, Kamatani Yoichiro, Bijlenga Philippe, Redon Richard, Woo Daniel, Werring David J, Broderick Joseph P, Lindgren Antti, von Und Zu Fraunberg Mikael, Jaaskelainen Juha E, Niemelä Mika, Gaal-Paavola Emilia I, Slowik Agnieszka, Pera Joanna, Worrall Bradford B, Rinkel Gabriel J E, Friedrich Christoph M, Verschuren W M Monique, Zwart John-Anker, Chen Zhengming, Millwood Iona Y, Liang Liming, Lin Kuang, Walters Robin G, Matsuda Koichi, Terao Chikashi, Akiyama Masato, Koido Masaru, van Eijk Kristel R, Alg Varinder S, Hostettler Isabel, Bourcier Romain, Morel Sandrine, van Rheenen Wouter, van der Spek Rick A A, Rouleau Guy A, Zhou Sirui, Rannikmäe Kristiina, Hveem Kristian, Willer Cristen J, Sandvei Marie Søfteland, Brumpton Ben M, Johnsen Marianne Bakke, Børte Sigrid, Winsvold Bendik S, Desal Hubert, Eugène François, Shotar Eimad, Gentric Jean-Christophe, Naggara Olivier, Dina Christian, van den Berg Leonard H, Houlden Henry, Sudlow Cathie L M, Bakker Mark K
Genetic Variants Are an Underlying Cause of Familial Intracranial Aneurysms.
Hostettler I, Houlden H, Werring D, Grieve J, Brown M, Kitchen N, Bulters D, Walsh D, Bonner S, Alg V, Davagnanam I, Vandrovcova J, O'Connor E, Bugiardini E, O'Callaghan B. Genetic Variants Are an Underlying Cause of Familial Intracranial Aneurysms. Neurology 2020; 96:e947-e955.
Oct 26, 2020Genetic Variants Are an Underlying Cause of Familial Intracranial Aneurysms.
Oct 26, 2020Neurology 2020; 96:e947-e955
Hostettler Isabel, Houlden Henry, Werring David J, Grieve Joan, Brown Martin M, Kitchen Neil, Bulters Diederik, Walsh Daniel, Bonner Stephen, Alg Varinder S, Davagnanam Indran, Vandrovcova Jana, O'Connor Emer, Bugiardini Enrico, O'Callaghan Benjamin
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
Longer term stroke risk in intracerebral haemorrhage survivors.
Banerjee G, Werring D, Jäger H, Brown M, Muir K, Houlden H, Lip G, Al-Shahi Salman R, Yousry T, Cohen H, Shakeshaft C, Hostettler I, Ambler G, Wilson D. Longer term stroke risk in intracerebral haemorrhage survivors. J Neurol Neurosurg Psychiatry 2020; 91:840-845.
Jun 17, 2020Longer term stroke risk in intracerebral haemorrhage survivors.
Jun 17, 2020J Neurol Neurosurg Psychiatry 2020; 91:840-845
Banerjee Gargi, Werring David J, Jäger Hans Rolf, Brown Martin M, Muir Keith, Houlden Henry, Lip Gregory Y H, Al-Shahi Salman Rustam, Yousry Tarek A, Cohen Hannah, Shakeshaft Clare, Hostettler Isabel, Ambler Gareth, Wilson Duncan