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5 matches for
Valdés Hernández MC.
Cerebral small vessel disease genomics and its implications across the lifespan
Sargurupremraj M,
Suzuki H,
Jian X,
Sarnowski C,
Evans TE,
Bis JC,
Eiriksdottir G,
Sakaue S,
Terzikhan N,
Habes M,
Zhao W,
Zhao W
and 105 more — show all
Armstrong NJ,
Hofer E,
Yanek LR,
Hagenaars SP,
Kumar RB,
van den Akker EB,
McWhirter RE,
Trompet S,
Mishra A,
Saba Y,
Satizabal CL,
Beaudet G,
Petit L,
Tsuchida A,
Zago L,
Schilling S,
Sigurdsson S,
Gottesman RF,
Lewis CE,
Aggarwal NT,
Lopez OL,
Smith JA,
Valdés Hernández MC,
van der Grond J,
Wright MJ,
Knol MJ,
Dörr M,
Thomson RJ,
Bordes C,
Le Grand Q,
Duperron MG,
Smith AV,
Knopman DS,
Schreiner PJ,
Evans DA,
Rotter JI,
Beiser AS,
Maniega SM,
Beekman M,
Trollor J,
Stott DJ,
Vernooij MW,
Wittfeld K,
Niessen WJ,
Soumaré A,
Boerwinkle E,
Sidney S,
Turner ST,
Davies G,
Thalamuthu A,
Völker U,
van Buchem MA,
Bryan RN,
Dupuis J,
Bastin ME,
Ames D,
Teumer A,
Amouyel P,
Kwok JB,
Bülow R,
Deary IJ,
Schofield PR,
Brodaty H,
Jiang J,
Tabara Y,
Setoh K,
Miyamoto S,
Yoshida K,
Nagata M,
Kamatani Y,
Matsuda F,
Psaty BM,
Bennett DA,
De Jager PL,
Mosley TH,
Sachdev PS,
Schmidt R,
Warren HR,
Evangelou E,
Trégouët DA,
Ikram MA,
Wen W,
DeCarli C,
Srikanth VK,
Jukema JW,
Slagboom EP,
Kardia SLR,
Okada Y,
Mazoyer B,
Wardlaw JM,
Nyquist PA,
Mather KA,
Grabe HJ,
Schmidt H,
Van Duijn CM,
Gudnason V,
Longstreth WT Jr,
Launer LJ,
Lathrop M,
Seshadri S,
Tzourio C,
Adams HH,
Matthews PM,
Fornage M,
Debette S
International Network against Thrombosis (INVENT) Consortium · International Headache Genomics Consortium (IHGC)
Nature communications · 2020 · PMID 33293549 · open access
12 pages+
Genetic architecture of subcortical brain structures in 38,851 individuals
Satizabal CL,
Adams HHH,
Hibar DP,
White CC,
Knol MJ,
Stein JL,
Scholz M,
Sargurupremraj M,
Jahanshad N,
Roshchupkin GV,
Smith AV,
Bis JC
and 277 more — show all
Jian X,
Luciano M,
Hofer E,
Teumer A,
van der Lee SJ,
Yang J,
Yanek LR,
Lee TV,
Li S,
Hu Y,
Koh JY,
Eicher JD,
Desrivières S,
Arias-Vasquez A,
Chauhan G,
Athanasiu L,
Rentería ME,
Kim S,
Hoehn D,
Armstrong NJ,
Chen Q,
Holmes AJ,
den Braber A,
Kloszewska I,
Andersson M,
Espeseth T,
Grimm O,
Abramovic L,
Alhusaini S,
Milaneschi Y,
Papmeyer M,
Axelsson T,
Ehrlich S,
Roiz-Santiañez R,
Kraemer B,
Håberg AK,
Jones HJ,
Pike GB,
Stein DJ,
Stevens A,
Bralten J,
Vernooij MW,
Harris TB,
Filippi I,
Witte AV,
Guadalupe T,
Wittfeld K,
Mosley TH,
Becker JT,
Doan NT,
Hagenaars SP,
Saba Y,
Cuellar-Partida G,
Amin N,
Hilal S,
Nho K,
Mirza-Schreiber N,
Arfanakis K,
Becker DM,
Ames D,
Goldman AL,
Lee PH,
Boomsma DI,
Lovestone S,
Giddaluru S,
Le Hellard S,
Mattheisen M,
Bohlken MM,
Kasperaviciute D,
Schmaal L,
Lawrie SM,
Agartz I,
Walton E,
Tordesillas-Gutierrez D,
Davies GE,
Shin J,
Ipser JC,
Vinke LN,
Hoogman M,
Jia T,
Burkhardt R,
Klein M,
Crivello F,
Janowitz D,
Carmichael O,
Haukvik UK,
Aribisala BS,
Schmidt H,
Strike LT,
Cheng CY,
Risacher SL,
Pütz B,
Fleischman DA,
Assareh AA,
Mattay VS,
Buckner RL,
Mecocci P,
Dale AM,
Cichon S,
Boks MP,
Matarin M,
Penninx BWJH,
Calhoun VD,
Chakravarty MM,
Marquand AF,
Macare C,
Kharabian Masouleh S,
Oosterlaan J,
Amouyel P,
Hegenscheid K,
Rotter JI,
Schork AJ,
Liewald DCM,
de Zubicaray GI,
Wong TY,
Shen L,
Sämann PG,
Brodaty H,
Roffman JL,
de Geus EJC,
Tsolaki M,
Erk S,
van Eijk KR,
Cavalleri GL,
van der Wee NJA,
McIntosh AM,
Gollub RL,
Bulayeva KB,
Bernard M,
Richards JS,
Himali JJ,
Loeffler M,
Rommelse N,
Hoffmann W,
Westlye LT,
Valdés Hernández MC,
Hansell NK,
van Erp TGM,
Wolf C,
Kwok JBJ,
Vellas B,
Heinz A,
Olde Loohuis LM,
Delanty N,
Ho BC,
Ching CRK,
Shumskaya E,
Singh B,
Hofman A,
van der Meer D,
Homuth G,
Psaty BM,
Bastin ME,
Montgomery GW,
Foroud TM,
Reppermund S,
Hottenga JJ,
Simmons A,
Meyer-Lindenberg A,
Cahn W,
Whelan CD,
van Donkelaar MMJ,
Yang Q,
Hosten N,
Green RC,
Thalamuthu A,
Mohnke S,
Hulshoff Pol HE,
Lin H,
Jack CR Jr,
Schofield PR,
Mühleisen TW,
Maillard P,
Potkin SG,
Wen W,
Fletcher E,
Toga AW,
Gruber O,
Huentelman M,
Davey Smith G,
Launer LJ,
Nyberg L,
Jönsson EG,
Crespo-Facorro B,
Koen N,
Greve DN,
Uitterlinden AG,
Weinberger DR,
Steen VM,
Fedko IO,
Groenewold NA,
Niessen WJ,
Toro R,
Tzourio C,
Longstreth WT Jr,
Ikram MK,
Smoller JW,
van Tol MJ,
Sussmann JE,
Paus T,
Lemaître H,
Schroeter ML,
Mazoyer B,
Andreassen OA,
Holsboer F,
Depondt C,
Veltman DJ,
Turner JA,
Pausova Z,
Schumann G,
van Rooij D,
Djurovic S,
Deary IJ,
McMahon KL,
Müller-Myhsok B,
Brouwer RM,
Soininen H,
Pandolfo M,
Wassink TH,
Cheung JW,
Wolfers T,
Martinot JL,
Zwiers MP,
Nauck M,
Melle I,
Martin NG,
Kanai R,
Westman E,
Kahn RS,
Sisodiya SM,
White T,
Saremi A,
van Bokhoven H,
Brunner HG,
Völzke H,
Wright MJ,
van 't Ent D,
Nöthen MM,
Ophoff RA,
Buitelaar JK,
Fernández G,
Sachdev PS,
Rietschel M,
van Haren NEM,
Fisher SE,
Beiser AS,
Francks C,
Saykin AJ,
Mather KA,
Romanczuk-Seiferth N,
Hartman CA,
DeStefano AL,
Heslenfeld DJ,
Weiner MW,
Walter H,
Hoekstra PJ,
Nyquist PA,
Franke B,
Bennett DA,
Grabe HJ,
Johnson AD,
Chen C,
van Duijn CM,
Lopez OL,
Fornage M,
Wardlaw JM,
Schmidt R,
DeCarli C,
De Jager PL,
Villringer A,
Debette S,
Gudnason V,
Medland SE,
Shulman JM,
Thompson PM,
Seshadri S,
Ikram MA
Nature genetics · 2019 · PMID 31636452
9 pages
Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease
Duperron MG,
Knol MJ,
Le Grand Q,
Evans TE,
Mishra A,
Tsuchida A,
Roshchupkin G,
Konuma T,
Trégouët DA,
Romero JR,
Frenzel S,
Luciano M
and 76 more — show all
Hofer E,
Bourgey M,
Dueker ND,
Delgado P,
Hilal S,
Tankard RM,
Dubost F,
Shin J,
Saba Y,
Armstrong NJ,
Bordes C,
Bastin ME,
Beiser A,
Brodaty H,
Bülow R,
Carrera C,
Chen C,
Cheng CY,
Deary IJ,
Gampawar PG,
Himali JJ,
Jiang J,
Kawaguchi T,
Li S,
Macalli M,
Marquis P,
Morris Z,
Muñoz Maniega S,
Miyamoto S,
Okawa M,
Paradise M,
Parva P,
Rundek T,
Sargurupremraj M,
Schilling S,
Setoh K,
Soukarieh O,
Tabara Y,
Teumer A,
Thalamuthu A,
Trollor JN,
Valdés Hernández MC,
Vernooij MW,
Völker U,
Wittfeld K,
Wong TY,
Wright MJ,
Zhang J,
Zhao W,
Zhu YC,
Schmidt H,
Sachdev PS,
Wen W,
Yoshida K,
Joutel A,
Satizabal CL,
Sacco RL,
Bourque G,
Lathrop M,
Paus T,
Fernandez-Cadenas I,
Yang Q,
Mazoyer B,
Boutinaud P,
Okada Y,
Grabe HJ,
Mather KA,
Schmidt R,
Joliot M,
Ikram MA,
Matsuda F,
Tzourio C,
Wardlaw JM,
Seshadri S,
Adams HHH,
Debette S
CHARGE consortium
Nature medicine · 2023 · PMID 37069360 · open access
3 pages
Identification of common variants associated with human hippocampal and intracranial volumes
Stein JL,
Medland SE,
Vasquez AA,
Hibar DP,
Senstad RE,
Winkler AM,
Toro R,
Appel K,
Bartecek R,
Bergmann Ø,
Bernard M,
Brown AA
and 190 more — show all
Cannon DM,
Chakravarty MM,
Christoforou A,
Domin M,
Grimm O,
Hollinshead M,
Holmes AJ,
Homuth G,
Hottenga JJ,
Langan C,
Lopez LM,
Hansell NK,
Hwang KS,
Kim S,
Laje G,
Lee PH,
Liu X,
Loth E,
Lourdusamy A,
Mattingsdal M,
Mohnke S,
Maniega SM,
Nho K,
Nugent AC,
O'Brien C,
Papmeyer M,
Pütz B,
Ramasamy A,
Rasmussen J,
Rijpkema M,
Risacher SL,
Roddey JC,
Rose EJ,
Ryten M,
Shen L,
Sprooten E,
Strengman E,
Teumer A,
Trabzuni D,
Turner J,
van Eijk K,
van Erp TG,
van Tol MJ,
Wittfeld K,
Wolf C,
Woudstra S,
Aleman A,
Alhusaini S,
Almasy L,
Binder EB,
Brohawn DG,
Cantor RM,
Carless MA,
Corvin A,
Czisch M,
Curran JE,
Davies G,
de Almeida MA,
Delanty N,
Depondt C,
Duggirala R,
Dyer TD,
Erk S,
Fagerness J,
Fox PT,
Freimer NB,
Gill M,
Göring HH,
Hagler DJ,
Hoehn D,
Holsboer F,
Hoogman M,
Hosten N,
Jahanshad N,
Johnson MP,
Kasperaviciute D,
Kent JW Jr,
Kochunov P,
Lancaster JL,
Lawrie SM,
Liewald DC,
Mandl R,
Matarin M,
Mattheisen M,
Meisenzahl E,
Melle I,
Moses EK,
Mühleisen TW,
Nauck M,
Nöthen MM,
Olvera RL,
Pandolfo M,
Pike GB,
Puls R,
Reinvang I,
Rentería ME,
Rietschel M,
Roffman JL,
Royle NA,
Rujescu D,
Savitz J,
Schnack HG,
Schnell K,
Seiferth N,
Smith C,
Steen VM,
Valdés Hernández MC,
Van den Heuvel M,
van der Wee NJ,
Van Haren NE,
Veltman JA,
Völzke H,
Walker R,
Westlye LT,
Whelan CD,
Agartz I,
Boomsma DI,
Cavalleri GL,
Dale AM,
Djurovic S,
Drevets WC,
Hagoort P,
Hall J,
Heinz A,
Jack CR Jr,
Foroud TM,
Le Hellard S,
Macciardi F,
Montgomery GW,
Poline JB,
Porteous DJ,
Sisodiya SM,
Starr JM,
Sussmann J,
Toga AW,
Veltman DJ,
Walter H,
Weiner MW,
Bis JC,
Ikram MA,
Smith AV,
Gudnason V,
Tzourio C,
Vernooij MW,
Launer LJ,
DeCarli C,
Seshadri S,
Andreassen OA,
Apostolova LG,
Bastin ME,
Blangero J,
Brunner HG,
Buckner RL,
Cichon S,
Coppola G,
de Zubicaray GI,
Deary IJ,
Donohoe G,
de Geus EJ,
Espeseth T,
Fernández G,
Glahn DC,
Grabe HJ,
Hardy J,
Hulshoff Pol HE,
Jenkinson M,
Kahn RS,
McDonald C,
McIntosh AM,
McMahon FJ,
McMahon KL,
Meyer-Lindenberg A,
Morris DW,
Müller-Myhsok B,
Nichols TE,
Ophoff RA,
Paus T,
Pausova Z,
Penninx BW,
Potkin SG,
Sämann PG,
Saykin AJ,
Schumann G,
Smoller JW,
Wardlaw JM,
Weale ME,
Martin NG,
Franke B,
Wright MJ,
Thompson PM
Alzheimer's Disease Neuroimaging Initiative · EPIGEN Consortium and 4 more consortia
Nature genetics · 2012 · PMID 22504417
1 page
Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume
Vojinovic D,
Adams HH,
Jian X,
Yang Q,
Smith AV,
Bis JC,
Teumer A,
Scholz M,
Armstrong NJ,
Hofer E,
Saba Y,
Luciano M
and 79 more — show all
Bernard M,
Trompet S,
Yang J,
Gillespie NA,
van der Lee SJ,
Neumann A,
Ahmad S,
Andreassen OA,
Ames D,
Amin N,
Arfanakis K,
Bastin ME,
Becker DM,
Beiser AS,
Beyer F,
Brodaty H,
Bryan RN,
Bülow R,
Dale AM,
De Jager PL,
Deary IJ,
DeCarli C,
Fleischman DA,
Gottesman RF,
van der Grond J,
Gudnason V,
Harris TB,
Homuth G,
Knopman DS,
Kwok JB,
Lewis CE,
Li S,
Loeffler M,
Lopez OL,
Maillard P,
El Marroun H,
Mather KA,
Mosley TH,
Muetzel RL,
Nauck M,
Nyquist PA,
Panizzon MS,
Pausova Z,
Psaty BM,
Rice K,
Rotter JI,
Royle N,
Satizabal CL,
Schmidt R,
Schofield PR,
Schreiner PJ,
Sidney S,
Stott DJ,
Thalamuthu A,
Uitterlinden AG,
Valdés Hernández MC,
Vernooij MW,
Wen W,
White T,
Witte AV,
Wittfeld K,
Wright MJ,
Yanek LR,
Tiemeier H,
Kremen WS,
Bennett DA,
Jukema JW,
Paus T,
Wardlaw JM,
Schmidt H,
Sachdev PS,
Villringer A,
Grabe HJ,
Longstreth WT,
van Duijn CM,
Launer LJ,
Seshadri S,
Ikram MA,
Fornage M
Nature communications · 2018 · PMID 30258056 · open access
1 page
Questions about this list
Why is my paper here? I never gave you permission.
Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
cites your work, and links to the paper on PubMed — which is what a citation is.
Your title and author list come from Europe PMC, the same public record a library
catalogue uses.
Why are all the authors listed instead of "et al."?
Because a study that needed 622 people is a different kind of study from one that
needed four, and "et al." erases that. Twelve names show and the rest are one click
away. Everyone is searchable, including the 187th name on a consortium paper —
that person exists and may be looking for it.
My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
inconsistent across databases; where two people share a form of a name we cannot
separate them, and we would rather be corrected than guess.
My paper is not here. Does that mean you rejected it?
No. This catalogue is assembled from what a small team could read, and it is
thinnest outside European-ancestry cohorts. A paper is absent because nobody has got
to it, not because it was assessed and turned down.
Which pages rest on a paper?
Each row lists them, up to six, and links to each one. The count beside a row is
how many pages cite it in total.
How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
resting on it and disappears if that page stops — there is no separate list to
keep in step, because the citation lives on the page that makes the claim.