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14 matches for
Mishra A.
New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
Springelkamp H,
Iglesias AI,
Mishra A,
Höhn R,
Wojciechowski R,
Khawaja AP,
Nag A,
Wang YX,
Wang JJ,
Cuellar-Partida G,
Gibson J,
Bailey JN
and 71 more — show all
Vithana EN,
Gharahkhani P,
Boutin T,
Ramdas WD,
Zeller T,
Luben RN,
Yonova-Doing E,
Viswanathan AC,
Yazar S,
Cree AJ,
Haines JL,
Koh JY,
Souzeau E,
Wilson JF,
Amin N,
Müller C,
Venturini C,
Kearns LS,
Kang JH,
Tham YC,
Zhou T,
van Leeuwen EM,
Nickels S,
Sanfilippo P,
Liao J,
van der Linde H,
Zhao W,
van Koolwijk LM,
Zheng L,
Rivadeneira F,
Baskaran M,
van der Lee SJ,
Perera S,
de Jong PT,
Oostra BA,
Uitterlinden AG,
Fan Q,
Hofman A,
Tai ES,
Vingerling JR,
Sim X,
Wolfs RC,
Teo YY,
Lemij HG,
Khor CC,
Willemsen R,
Lackner KJ,
Aung T,
Jansonius NM,
Montgomery G,
Wild PS,
Young TL,
Burdon KP,
Hysi PG,
Pasquale LR,
Wong TY,
Klaver CC,
Hewitt AW,
Jonas JB,
Mitchell P,
Lotery AJ,
Foster PJ,
Vitart V,
Pfeiffer N,
Craig JE,
Mackey DA,
Hammond CJ,
Wiggs JL,
Cheng CY,
van Duijn CM,
MacGregor S
NEIGHBORHOOD Consortium
Human molecular genetics · 2017 · PMID 28073927
12 pages+
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases
Iglesias AI,
Mishra A,
Vitart V,
Bykhovskaya Y,
Höhn R,
Springelkamp H,
Cuellar-Partida G,
Gharahkhani P,
Bailey JNC,
Willoughby CE,
Li X,
Yazar S
and 47 more — show all
Nag A,
Khawaja AP,
Polašek O,
Siscovick D,
Mitchell P,
Tham YC,
Haines JL,
Kearns LS,
Hayward C,
Shi Y,
van Leeuwen EM,
Taylor KD,
Bonnemaijer P,
Rotter JI,
Martin NG,
Zeller T,
Mills RA,
Souzeau E,
Staffieri SE,
Jonas JB,
Schmidtmann I,
Boutin T,
Kang JH,
Lucas SEM,
Wong TY,
Beutel ME,
Wilson JF,
Uitterlinden AG,
Vithana EN,
Foster PJ,
Hysi PG,
Hewitt AW,
Khor CC,
Pasquale LR,
Montgomery GW,
Klaver CCW,
Aung T,
Pfeiffer N,
Mackey DA,
Hammond CJ,
Cheng CY,
Craig JE,
Rabinowitz YS,
Wiggs JL,
Burdon KP,
van Duijn CM,
MacGregor S
Blue Mountains Eye Study—GWAS group · NEIGHBORHOOD Consortium and 1 more consortia
Nature communications · 2018 · PMID 29760442 · open access
12 pages+
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+
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
Verhoeven VJ,
Hysi PG,
Wojciechowski R,
Fan Q,
Guggenheim JA,
Höhn R,
MacGregor S,
Hewitt AW,
Nag A,
Cheng CY,
Yonova-Doing E,
Zhou X
and 96 more — show all
Ikram MK,
Buitendijk GH,
McMahon G,
Kemp JP,
Pourcain BS,
Simpson CL,
Mäkelä KM,
Lehtimäki T,
Kähönen M,
Paterson AD,
Hosseini SM,
Wong HS,
Xu L,
Jonas JB,
Pärssinen O,
Wedenoja J,
Yip SP,
Ho DW,
Pang CP,
Chen LJ,
Burdon KP,
Craig JE,
Klein BE,
Klein R,
Haller T,
Metspalu A,
Khor CC,
Tai ES,
Aung T,
Vithana E,
Tay WT,
Barathi VA,
Chen P,
Li R,
Liao J,
Zheng Y,
Ong RT,
Döring A,
Evans DM,
Timpson NJ,
Verkerk AJ,
Meitinger T,
Raitakari O,
Hawthorne F,
Spector TD,
Karssen LC,
Pirastu M,
Murgia F,
Ang W,
Mishra A,
Montgomery GW,
Pennell CE,
Cumberland PM,
Cotlarciuc I,
Mitchell P,
Wang JJ,
Schache M,
Janmahasatian S,
Igo RP Jr,
Lass JH,
Chew E,
Iyengar SK,
Gorgels TG,
Rudan I,
Hayward C,
Wright AF,
Polasek O,
Vatavuk Z,
Wilson JF,
Fleck B,
Zeller T,
Mirshahi A,
Müller C,
Uitterlinden AG,
Rivadeneira F,
Vingerling JR,
Hofman A,
Oostra BA,
Amin N,
Bergen AA,
Teo YY,
Rahi JS,
Vitart V,
Williams C,
Baird PN,
Wong TY,
Oexle K,
Pfeiffer N,
Mackey DA,
Young TL,
van Duijn CM,
Saw SM,
Bailey-Wilson JE,
Stambolian D,
Klaver CC,
Hammond CJ
Consortium for Refractive Error and Myopia (CREAM) · Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Research Group and 2 more consortia
Nature genetics · 2013 · PMID 23396134
6 pages
Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology
Springelkamp H,
Mishra A,
Hysi PG,
Gharahkhani P,
Höhn R,
Khor CC,
Cooke Bailey JN,
Luo X,
Ramdas WD,
Vithana E,
Koh V,
Yazar S
and 45 more — show all
Xu L,
Forward H,
Kearns LS,
Amin N,
Iglesias AI,
Sim KS,
van Leeuwen EM,
Demirkan A,
van der Lee S,
Loon SC,
Rivadeneira F,
Nag A,
Sanfilippo PG,
Schillert A,
de Jong PT,
Oostra BA,
Uitterlinden AG,
Hofman A,
Zhou T,
Burdon KP,
Spector TD,
Lackner KJ,
Saw SM,
Vingerling JR,
Teo YY,
Pasquale LR,
Wolfs RC,
Lemij HG,
Tai ES,
Jonas JB,
Cheng CY,
Aung T,
Jansonius NM,
Klaver CC,
Craig JE,
Young TL,
Haines JL,
MacGregor S,
Mackey DA,
Pfeiffer N,
Wong TY,
Wiggs JL,
Hewitt AW,
van Duijn CM,
Hammond CJ
NEIGHBORHOOD Consortium
Genetic epidemiology · 2015 · PMID 25631615
6 pages
Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate
Mishra A,
Duplaà C,
Vojinovic D,
Suzuki H,
Sargurupremraj M,
Sargurupremraj M,
Zilhão NR,
Li S,
Bartz TM,
Jian X,
Zhao W,
Hofer E
and 56 more — show all
Wittfeld K,
Harris SE,
van der Auwera-Palitschka S,
Luciano M,
Bis JC,
Adams HHH,
Satizabal CL,
Gottesman RF,
Gampawar PG,
Bülow R,
Weiss S,
Yu M,
Bastin ME,
Lopez OL,
Vernooij MW,
Beiser AS,
Völker U,
Kacprowski T,
Soumare A,
Smith JA,
Knopman DS,
Morris Z,
Zhu Y,
Rotter JI,
Dufouil C,
Valdés Hernández M,
Muñoz Maniega S,
Lathrop M,
Boerwinkle E,
Schmidt R,
Ihara M,
Mazoyer B,
Yang Q,
Joutel A,
Tournier-Lasserve E,
Launer LJ,
Deary IJ,
Mosley TH,
Amouyel P,
DeCarli CS,
Psaty BM,
Tzourio C,
Kardia SLR,
Grabe HJ,
Teumer A,
van Duijn CM,
Schmidt H,
Wardlaw JM,
Ikram MA,
Fornage M,
Gudnason V,
Seshadri S,
Matthews PM,
Longstreth WT,
Couffinhal T,
Debette S
Brain : a journal of neurology · 2022 · PMID 35511193 · open access
6 pages
Stroke genetics informs drug discovery and risk prediction across ancestries
Mishra A,
Malik R,
Hachiya T,
Jürgenson T,
Namba S,
Posner DC,
Kamanu FK,
Koido M,
Le Grand Q,
Shi M,
He Y,
Georgakis MK
and 175 more — show all
Caro I,
Krebs K,
Liaw YC,
Vaura FC,
Lin K,
Winsvold BS,
Srinivasasainagendra V,
Parodi L,
Bae HJ,
Chauhan G,
Chong MR,
Tomppo L,
Akinyemi R,
Roshchupkin GV,
Habib N,
Jee YH,
Thomassen JQ,
Abedi V,
Cárcel-Márquez J,
Nygaard M,
Leonard HL,
Yang C,
Yonova-Doing E,
Knol MJ,
Lewis AJ,
Judy RL,
Ago T,
Amouyel P,
Armstrong ND,
Bakker MK,
Bartz TM,
Bennett DA,
Bis JC,
Bordes C,
Børte S,
Cain A,
Ridker PM,
Cho K,
Chen Z,
Cruchaga C,
Cole JW,
de Jager PL,
de Cid R,
Endres M,
Ferreira LE,
Geerlings MI,
Gasca NC,
Gudnason V,
Hata J,
He J,
Heath AK,
Ho YL,
Havulinna AS,
Hopewell JC,
Hyacinth HI,
Inouye M,
Jacob MA,
Jeon CE,
Jern C,
Kamouchi M,
Keene KL,
Kitazono T,
Kittner SJ,
Konuma T,
Kumar A,
Lacaze P,
Launer LJ,
Lee KJ,
Lepik K,
Li J,
Li L,
Manichaikul A,
Markus HS,
Marston NA,
Meitinger T,
Mitchell BD,
Montellano FA,
Morisaki T,
Mosley TH,
Nalls MA,
Nordestgaard BG,
O'Donnell MJ,
Okada Y,
Onland-Moret NC,
Ovbiagele B,
Peters A,
Psaty BM,
Rich SS,
Rosand J,
Sabatine MS,
Sacco RL,
Saleheen D,
Sandset EC,
Salomaa V,
Sargurupremraj M,
Sasaki M,
Satizabal CL,
Schmidt CO,
Shimizu A,
Smith NL,
Sloane KL,
Sutoh Y,
Sun YV,
Tanno K,
Tiedt S,
Tatlisumak T,
Torres-Aguila NP,
Tiwari HK,
Trégouët DA,
Trompet S,
Tuladhar AM,
Tybjærg-Hansen A,
van Vugt M,
Vibo R,
Verma SS,
Wiggins KL,
Wennberg P,
Woo D,
Wilson PWF,
Xu H,
Yang Q,
Yoon K,
Millwood IY,
Gieger C,
Ninomiya T,
Grabe HJ,
Jukema JW,
Rissanen IL,
Strbian D,
Kim YJ,
Chen PH,
Mayerhofer E,
Howson JMM,
Irvin MR,
Adams H,
Wassertheil-Smoller S,
Christensen K,
Ikram MA,
Rundek T,
Worrall BB,
Lathrop GM,
Riaz M,
Simonsick EM,
Kõrv J,
França PHC,
Zand R,
Prasad K,
Frikke-Schmidt R,
de Leeuw FE,
Liman T,
Haeusler KG,
Ruigrok YM,
Heuschmann PU,
Longstreth WT,
Jung KJ,
Bastarache L,
Paré G,
Damrauer SM,
Chasman DI,
Rotter JI,
Anderson CD,
Zwart JA,
Niiranen TJ,
Fornage M,
Liaw YP,
Seshadri S,
Fernández-Cadenas I,
Walters RG,
Ruff CT,
Owolabi MO,
Huffman JE,
Milani L,
Kamatani Y,
Dichgans M,
Debette S
COMPASS Consortium · INVENT Consortium and 13 more consortia
Nature · 2022 · PMID 36180795 · open access
5 pages
Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers
Jansen IE,
van der Lee SJ,
Gomez-Fonseca D,
de Rojas I,
Dalmasso MC,
Grenier-Boley B,
Zettergren A,
Mishra A,
Ali M,
Andrade V,
Bellenguez C,
Kleineidam L
and 134 more — show all
Küçükali F,
Sung YJ,
Tesí N,
Vromen EM,
Wightman DP,
Alcolea D,
Alegret M,
Alvarez I,
Amouyel P,
Athanasiu L,
Bahrami S,
Bailly H,
Belbin O,
Bergh S,
Bertram L,
Biessels GJ,
Blennow K,
Blesa R,
Boada M,
Boland A,
Buerger K,
Carracedo Á,
Cervera-Carles L,
Chene G,
Claassen JAHR,
Debette S,
Deleuze JF,
de Deyn PP,
Diehl-Schmid J,
Djurovic S,
Dols-Icardo O,
Dufouil C,
Duron E,
Düzel E,
Fladby T,
Fortea J,
Frölich L,
García-González P,
Garcia-Martinez M,
Giegling I,
Goldhardt O,
Gobom J,
Grimmer T,
Haapasalo A,
Hampel H,
Hanon O,
Hausner L,
Heilmann-Heimbach S,
Helisalmi S,
Heneka MT,
Hernández I,
Herukka SK,
Holstege H,
Jarholm J,
Kern S,
Knapskog AB,
Koivisto AM,
Kornhuber J,
Kuulasmaa T,
Lage C,
Laske C,
Leinonen V,
Lewczuk P,
Lleó A,
de Munain AL,
Lopez-Garcia S,
Maier W,
Marquié M,
Mol MO,
Montrreal L,
Moreno F,
Moreno-Grau S,
Nicolas G,
Nöthen MM,
Orellana A,
Pålhaugen L,
Papma JM,
Pasquier F,
Perneczky R,
Peters O,
Pijnenburg YAL,
Popp J,
Posthuma D,
Pozueta A,
Priller J,
Puerta R,
Quintela I,
Ramakers I,
Rodriguez-Rodriguez E,
Rujescu D,
Saltvedt I,
Sanchez-Juan P,
Scheltens P,
Scherbaum N,
Schmid M,
Schneider A,
Selbæk G,
Selnes P,
Shadrin A,
Skoog I,
Soininen H,
Tárraga L,
Teipel S,
Tijms B,
Tsolaki M,
Van Broeckhoven C,
Van Dongen J,
van Swieten JC,
Vandenberghe R,
Vidal JS,
Visser PJ,
Vogelgsang J,
Waern M,
Wagner M,
Wiltfang J,
Wittens MMJ,
Zetterberg H,
Zulaica M,
van Duijn CM,
Bjerke M,
Engelborghs S,
Jessen F,
Teunissen CE,
Pastor P,
Hiltunen M,
Ingelsson M,
Andreassen OA,
Clarimón J,
Sleegers K,
Ruiz A,
Ramirez A,
Cruchaga C,
Lambert JC,
van der Flier W
EADB consortium · GR@ACE study group
Acta neuropathologica · 2022 · PMID 36066633 · open access
3 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
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error
Cheng CY,
Schache M,
Ikram MK,
Young TL,
Guggenheim JA,
Vitart V,
MacGregor S,
Verhoeven VJ,
Barathi VA,
Liao J,
Hysi PG,
Bailey-Wilson JE
and 96 more — show all
St Pourcain B,
Kemp JP,
McMahon G,
Timpson NJ,
Evans DM,
Montgomery GW,
Mishra A,
Wang YX,
Wang JJ,
Rochtchina E,
Polasek O,
Wright AF,
Amin N,
van Leeuwen EM,
Wilson JF,
Pennell CE,
van Duijn CM,
de Jong PT,
Vingerling JR,
Zhou X,
Chen P,
Li R,
Tay WT,
Zheng Y,
Chew M,
Burdon KP,
Craig JE,
Iyengar SK,
Igo RP Jr,
Lass JH Jr,
Chew EY,
Haller T,
Mihailov E,
Metspalu A,
Wedenoja J,
Simpson CL,
Wojciechowski R,
Höhn R,
Mirshahi A,
Zeller T,
Pfeiffer N,
Lackner KJ,
Bettecken T,
Meitinger T,
Oexle K,
Pirastu M,
Portas L,
Nag A,
Williams KM,
Yonova-Doing E,
Klein R,
Klein BE,
Hosseini SM,
Paterson AD,
Makela KM,
Lehtimaki T,
Kahonen M,
Raitakari O,
Yoshimura N,
Matsuda F,
Chen LJ,
Pang CP,
Yip SP,
Yap MK,
Meguro A,
Mizuki N,
Inoko H,
Foster PJ,
Zhao JH,
Vithana E,
Tai ES,
Fan Q,
Xu L,
Campbell H,
Fleck B,
Rudan I,
Aung T,
Hofman A,
Uitterlinden AG,
Bencic G,
Khor CC,
Forward H,
Pärssinen O,
Mitchell P,
Rivadeneira F,
Hewitt AW,
Williams C,
Oostra BA,
Teo YY,
Hammond CJ,
Stambolian D,
Mackey DA,
Klaver CC,
Wong TY,
Saw SM,
Baird PN
Consortium for Refractive Error and Myopia · Fuchs' Genetics Multi-Center Study Group and 2 more consortia
American journal of human genetics · 2013 · PMID 24144296
2 pages
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process
Springelkamp H,
Höhn R,
Mishra A,
Hysi PG,
Khor CC,
Loomis SJ,
Bailey JN,
Gibson J,
Thorleifsson G,
Janssen SF,
Luo X,
Ramdas WD
and 66 more — show all
Vithana E,
Nongpiur ME,
Montgomery GW,
Xu L,
Mountain JE,
Gharahkhani P,
Lu Y,
Amin N,
Karssen LC,
Sim KS,
van Leeuwen EM,
Iglesias AI,
Verhoeven VJ,
Hauser MA,
Loon SC,
Despriet DD,
Nag A,
Venturini C,
Sanfilippo PG,
Schillert A,
Kang JH,
Landers J,
Jonasson F,
Cree AJ,
van Koolwijk LM,
Rivadeneira F,
Souzeau E,
Jonsson V,
Menon G,
Weinreb RN,
de Jong PT,
Oostra BA,
Uitterlinden AG,
Hofman A,
Ennis S,
Thorsteinsdottir U,
Burdon KP,
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Blue Mountains Eye Study—GWAS group · NEIGHBORHOOD Consortium and 1 more consortia
Nature communications · 2014 · PMID 25241763 · open access
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Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis
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Edkins S,
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LeishGEN Consortium · Wellcome Trust Case Control Consortium 2
Nature genetics · 2013 · PMID 23291585 · open access
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Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels
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Communications biology · 2022 · PMID 35396452 · open access
1 page
Genome-wide association study meta-analysis of neurofilament light (NfL) levels in blood reveals novel loci related to neurodegeneration
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Bouteloup V,
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Communications biology · 2024 · PMID 39251807 · open access
1 page
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