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17 matches for
Song Y.
Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
Khawaja AP,
Cooke Bailey JN,
Wareham NJ,
Scott RA,
Simcoe M,
Igo RP Jr,
Song YE,
Wojciechowski R,
Cheng CY,
Khaw PT,
Pasquale LR,
Haines JL
and 4 more — show all
UK Biobank Eye and Vision Consortium · NEIGHBORHOOD Consortium
Nature genetics · 2018 · PMID 29785010 · open access
12 pages+
Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates
Dashti HS,
Jones SE,
Wood AR,
Lane JM,
van Hees VT,
Wang H,
Rhodes JA,
Song Y,
Patel K,
Anderson SG,
Beaumont RN,
Bechtold DA
and 20 more — show all
Bowden J,
Cade BE,
Garaulet M,
Kyle SD,
Little MA,
Loudon AS,
Luik AI,
Scheer FAJL,
Spiegelhalder K,
Tyrrell J,
Gottlieb DJ,
Tiemeier H,
Ray DW,
Purcell SM,
Frayling TM,
Redline S,
Lawlor DA,
Rutter MK,
Weedon MN,
Saxena R
Nature communications · 2019 · PMID 30846698 · open access
12 pages+
Multi-ancestry genome-wide analysis identifies shared genetic effects and common genetic variants for self-reported sleep duration
Scammell BH,
Tchio C,
Song Y,
Nishiyama T,
Louie TL,
Dashti HS,
Nakatochi M,
Zee PC,
Daghlas I,
Momozawa Y,
Cai J,
Ollila HM
and 6 more — show all
Human molecular genetics · 2023 · PMID 37384397
12 pages+
Translational genomics of osteoarthritis in 1,962,069 individuals
Hatzikotoulas K,
Southam L,
Stefansdottir L,
Boer CG,
McDonald ML,
Pett JP,
Park YC,
Tuerlings M,
Mulders R,
Barysenka A,
Arruda AL,
Tragante V
and 162 more — show all
Rocco A,
Bittner N,
Chen S,
Horn S,
Srinivasasainagendra V,
To K,
Katsoula G,
Kreitmaier P,
Tenghe AMM,
Gilly A,
Arbeeva L,
Chen LG,
de Pins AM,
Dochtermann D,
Henkel C,
Höijer J,
Ito S,
Lind PA,
Lukusa-Sawalena B,
Minn AKK,
Mola-Caminal M,
Narita A,
Nguyen C,
Reimann E,
Silberstein MD,
Skogholt AH,
Tiwari HK,
Yau MS,
Yue M,
Zhao W,
Zhao W,
Zhou JJ,
Alexiadis G,
Banasik K,
Brunak S,
Campbell A,
Cheung JTS,
Dowsett J,
Faquih T,
Faul JD,
Fei L,
Fenstad AM,
Funayama T,
Gabrielsen ME,
Gocho C,
Gromov K,
Hansen T,
Hudjashov G,
Ingvarsson T,
Johnson JS,
Jonsson H,
Kakehi S,
Karjalainen J,
Kasbohm E,
Lemmelä S,
Lin K,
Liu X,
Loef M,
Mangino M,
McCartney D,
Millwood IY,
Richman J,
Roberts MB,
Ryan KA,
Samartzis D,
Shivakumar M,
Skou ST,
Sugimoto S,
Suzuki K,
Takuwa H,
Teder-Laving M,
Thomas L,
Tomizuka K,
Turman C,
Weiss S,
Wu TT,
Zengini E,
Zhang Y,
Ferreira MAR,
Babis G,
Baras A,
Barker T,
Carey DJ,
Cheah KSE,
Chen Z,
Cheung JP,
Daly M,
de Mutsert R,
Eaton CB,
Erikstrup C,
Furnes ON,
Golightly YM,
Gudbjartsson DF,
Hailer NP,
Hayward C,
Hochberg MC,
Homuth G,
Huckins LM,
Hveem K,
Ikegawa S,
Ishijima M,
Isomura M,
Jones M,
Kang JH,
Kardia SLR,
Kloppenburg M,
Kraft P,
Kumahashi N,
Kuwata S,
Lee MTM,
Lee PH,
Lerner R,
Li L,
Lietman SA,
Lotta L,
Lupton MK,
Mägi R,
Martin NG,
McAlindon TE,
Medland SE,
Michaëlsson K,
Mitchell BD,
Mook-Kanamori DO,
Morris AP,
Nabika T,
Nagami F,
Nelson AE,
Ostrowski SR,
Palotie A,
Pedersen OB,
Rosendaal FR,
Sakurai-Yageta M,
Schmidt CO,
Sham PC,
Singh JA,
Smelser DT,
Smith JA,
Song YQ,
Sørensen E,
Tamiya G,
Tamura Y,
Terao C,
Thorleifsson G,
Troelsen A,
Tsezou A,
Uchio Y,
Uitterlinden AG,
Ullum H,
Valdes AM,
van Heel DA,
Walters RG,
Weir DR,
Wilkinson JM,
Winsvold BS,
Yamamoto M,
Zwart JA,
Stefansson K,
Meulenbelt I,
Teichmann SA,
van Meurs JBJ,
Styrkarsdottir U,
Zeggini E
arcOGEN Consortium · ARGO Consortium and 7 more consortia
Nature · 2025 · PMID 40205036 · open access
12 pages+
New insights into the genetic etiology of Alzheimer's disease and related dementias
Bellenguez C,
Küçükali F,
Jansen IE,
Kleineidam L,
Moreno-Grau S,
Amin N,
Naj AC,
Campos-Martin R,
Grenier-Boley B,
Andrade V,
Holmans PA,
Boland A
and 391 more — show all
Damotte V,
van der Lee SJ,
Costa MR,
Kuulasmaa T,
Yang Q,
de Rojas I,
Bis JC,
Yaqub A,
Prokic I,
Chapuis J,
Ahmad S,
Giedraitis V,
Aarsland D,
Garcia-Gonzalez P,
Abdelnour C,
Alarcón-Martín E,
Alcolea D,
Alegret M,
Alvarez I,
Álvarez V,
Armstrong NJ,
Tsolaki A,
Antúnez C,
Appollonio I,
Arcaro M,
Archetti S,
Pastor AA,
Arosio B,
Athanasiu L,
Bailly H,
Banaj N,
Baquero M,
Barral S,
Beiser A,
Pastor AB,
Below JE,
Benchek P,
Benussi L,
Berr C,
Besse C,
Bessi V,
Binetti G,
Bizarro A,
Blesa R,
Boada M,
Boerwinkle E,
Borroni B,
Boschi S,
Bossù P,
Bråthen G,
Bressler J,
Bresner C,
Brodaty H,
Brookes KJ,
Brusco LI,
Buiza-Rueda D,
Bûrger K,
Burholt V,
Bush WS,
Calero M,
Cantwell LB,
Chene G,
Chung J,
Cuccaro ML,
Carracedo Á,
Cecchetti R,
Cervera-Carles L,
Charbonnier C,
Chen HH,
Chillotti C,
Ciccone S,
Claassen JAHR,
Clark C,
Conti E,
Corma-Gómez A,
Costantini E,
Custodero C,
Daian D,
Dalmasso MC,
Daniele A,
Dardiotis E,
Dartigues JF,
de Deyn PP,
de Paiva Lopes K,
de Witte LD,
Debette S,
Deckert J,
Del Ser T,
Denning N,
DeStefano A,
Dichgans M,
Diehl-Schmid J,
Diez-Fairen M,
Rossi PD,
Djurovic S,
Duron E,
Düzel E,
Dufouil C,
Eiriksdottir G,
Engelborghs S,
Escott-Price V,
Espinosa A,
Ewers M,
Faber KM,
Fabrizio T,
Nielsen SF,
Fardo DW,
Farotti L,
Fenoglio C,
Fernández-Fuertes M,
Ferrari R,
Ferreira CB,
Ferri E,
Fin B,
Fischer P,
Fladby T,
Fließbach K,
Fongang B,
Fornage M,
Fortea J,
Foroud TM,
Fostinelli S,
Fox NC,
Franco-Macías E,
Bullido MJ,
Frank-García A,
Froelich L,
Fulton-Howard B,
Galimberti D,
García-Alberca JM,
García-González P,
Garcia-Madrona S,
Garcia-Ribas G,
Ghidoni R,
Giegling I,
Giorgio G,
Goate AM,
Goldhardt O,
Gomez-Fonseca D,
González-Pérez A,
Graff C,
Grande G,
Green E,
Grimmer T,
Grünblatt E,
Grunin M,
Gudnason V,
Guetta-Baranes T,
Haapasalo A,
Hadjigeorgiou G,
Haines JL,
Hamilton-Nelson KL,
Hampel H,
Hanon O,
Hardy J,
Hartmann AM,
Hausner L,
Harwood J,
Heilmann-Heimbach S,
Helisalmi S,
Heneka MT,
Hernández I,
Herrmann MJ,
Hoffmann P,
Holmes C,
Holstege H,
Vilas RH,
Hulsman M,
Humphrey J,
Biessels GJ,
Jian X,
Johansson C,
Jun GR,
Kastumata Y,
Kauwe J,
Kehoe PG,
Kilander L,
Ståhlbom AK,
Kivipelto M,
Koivisto A,
Kornhuber J,
Kosmidis MH,
Kukull WA,
Kuksa PP,
Kunkle BW,
Kuzma AB,
Lage C,
Laukka EJ,
Launer L,
Lauria A,
Lee CY,
Lehtisalo J,
Lerch O,
Lleó A,
Longstreth W Jr,
Lopez O,
de Munain AL,
Love S,
Löwemark M,
Luckcuck L,
Lunetta KL,
Ma Y,
Macías J,
MacLeod CA,
Maier W,
Mangialasche F,
Spallazzi M,
Marquié M,
Marshall R,
Martin ER,
Montes AM,
Rodríguez CM,
Masullo C,
Mayeux R,
Mead S,
Mecocci P,
Medina M,
Meggy A,
Mehrabian S,
Mendoza S,
Menéndez-González M,
Mir P,
Moebus S,
Mol M,
Molina-Porcel L,
Montrreal L,
Morelli L,
Moreno F,
Morgan K,
Mosley T,
Nöthen MM,
Muchnik C,
Mukherjee S,
Nacmias B,
Ngandu T,
Nicolas G,
Nordestgaard BG,
Olaso R,
Orellana A,
Orsini M,
Ortega G,
Padovani A,
Paolo C,
Papenberg G,
Parnetti L,
Pasquier F,
Pastor P,
Peloso G,
Pérez-Cordón A,
Pérez-Tur J,
Pericard P,
Peters O,
Pijnenburg YAL,
Pineda JA,
Piñol-Ripoll G,
Pisanu C,
Polak T,
Popp J,
Posthuma D,
Priller J,
Puerta R,
Quenez O,
Quintela I,
Thomassen JQ,
Rábano A,
Rainero I,
Rajabli F,
Ramakers I,
Real LM,
Reinders MJT,
Reitz C,
Reyes-Dumeyer D,
Ridge P,
Riedel-Heller S,
Riederer P,
Roberto N,
Rodriguez-Rodriguez E,
Rongve A,
Allende IR,
Rosende-Roca M,
Royo JL,
Rubino E,
Rujescu D,
Sáez ME,
Sakka P,
Saltvedt I,
Sanabria Á,
Sánchez-Arjona MB,
Sanchez-Garcia F,
Juan PS,
Sánchez-Valle R,
Sando SB,
Sarnowski C,
Satizabal CL,
Scamosci M,
Scarmeas N,
Scarpini E,
Scheltens P,
Scherbaum N,
Scherer M,
Schmid M,
Schneider A,
Schott JM,
Selbæk G,
Seripa D,
Serrano M,
Sha J,
Shadrin AA,
Skrobot O,
Slifer S,
Snijders GJL,
Soininen H,
Solfrizzi V,
Solomon A,
Song Y,
Sorbi S,
Sotolongo-Grau O,
Spalletta G,
Spottke A,
Squassina A,
Stordal E,
Tartan JP,
Tárraga L,
Tesí N,
Thalamuthu A,
Thomas T,
Tosto G,
Traykov L,
Tremolizzo L,
Tybjærg-Hansen A,
Uitterlinden A,
Ullgren A,
Ulstein I,
Valero S,
Valladares O,
Broeckhoven CV,
Vance J,
Vardarajan BN,
van der Lugt A,
Dongen JV,
van Rooij J,
van Swieten J,
Vandenberghe R,
Verhey F,
Vidal JS,
Vogelgsang J,
Vyhnalek M,
Wagner M,
Wallon D,
Wang LS,
Wang R,
Weinhold L,
Wiltfang J,
Windle G,
Woods B,
Yannakoulia M,
Zare H,
Zhao Y,
Zhang X,
Zhu C,
Zulaica M,
Farrer LA,
Psaty BM,
Ghanbari M,
Raj T,
Sachdev P,
Mather K,
Jessen F,
Ikram MA,
de Mendonça A,
Hort J,
Tsolaki M,
Pericak-Vance MA,
Amouyel P,
Williams J,
Frikke-Schmidt R,
Clarimon J,
Deleuze JF,
Rossi G,
Seshadri S,
Andreassen OA,
Ingelsson M,
Hiltunen M,
Sleegers K,
Schellenberg GD,
van Duijn CM,
Sims R,
van der Flier WM,
Ruiz A,
Ramirez A,
Lambert JC
EADB · GR@ACE and 7 more consortia
Nature genetics · 2022 · PMID 35379992 · open access
9 pages
Biological and clinical insights from genetics of insomnia symptoms
Lane JM,
Jones SE,
Dashti HS,
Wood AR,
Aragam KG,
van Hees VT,
Strand LB,
Winsvold BS,
Wang H,
Bowden J,
Song Y,
Patel K
and 31 more — show all
Anderson SG,
Beaumont RN,
Bechtold DA,
Cade BE,
Haas M,
Kathiresan S,
Little MA,
Luik AI,
Loudon AS,
Purcell S,
Richmond RC,
Scheer FAJL,
Schormair B,
Tyrrell J,
Winkelman JW,
Winkelmann J,
Hveem K,
Zhao C,
Nielsen JB,
Willer CJ,
Redline S,
Spiegelhalder K,
Kyle SD,
Ray DW,
Zwart JA,
Brumpton B,
Frayling TM,
Lawlor DA,
Rutter MK,
Weedon MN,
Saxena R
HUNT All In Sleep
Nature genetics · 2019 · PMID 30804566 · open access
6 pages
Genetic analysis of dietary intake identifies new loci and functional links with metabolic traits
Merino J,
Dashti HS,
Sarnowski C,
Lane JM,
Todorov PV,
Udler MS,
Song Y,
Wang H,
Kim J,
Tucker C,
Campbell J,
Tanaka T
and 8 more — show all
Nature human behaviour · 2022 · PMID 34426670
4 pages
Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease
Garcia-Barcelo MM,
Tang CS,
Ngan ES,
Lui VC,
Chen Y,
So MT,
Leon TY,
Miao XP,
Shum CK,
Liu FQ,
Yeung MY,
Yuan ZW
and 12 more — show all
Guo WH,
Liu L,
Sun XB,
Huang LM,
Tou JF,
Song YQ,
Chan D,
Cheung KM,
Wong KK,
Cherny SS,
Sham PC,
Tam PK
Proceedings of the National Academy of Sciences of the United States of America · 2009 · PMID 19196962
2 pages
Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2
Garcia-Barceló MM,
Yeung MY,
Miao XP,
Tang CS,
Cheng G,
So MT,
Ngan ES,
Lui VC,
Chen Y,
Liu XL,
Hui KJ,
Li L
and 13 more — show all
Guo WH,
Sun XB,
Tou JF,
Chan KW,
Wu XZ,
Song YQ,
Chan D,
Cheung K,
Chung PH,
Wong KK,
Sham PC,
Cherny SS,
Tam PK
Human molecular genetics · 2010 · PMID 20460270
2 pages
Genome-wide association study identifies new susceptibility loci for adolescent idiopathic scoliosis in Chinese girls
Zhu Z,
Tang NL,
Xu L,
Qin X,
Mao S,
Song Y,
Liu L,
Li F,
Liu P,
Yi L,
Chang J,
Jiang L
and 25 more — show all
Ng BK,
Shi B,
Zhang W,
Qiao J,
Sun X,
Qiu X,
Wang Z,
Wang F,
Xie D,
Chen L,
Chen Z,
Jin M,
Han X,
Hu Z,
Zhang Z,
Liu Z,
Zhu F,
Qian BP,
Yu Y,
Wang B,
Lee KM,
Lee WYW,
Lam TP,
Qiu Y,
Cheng JC
Nature communications · 2015 · PMID 26394188 · open access
2 pages
Genome-wide association study of breakfast skipping links clock regulation with food timing
Dashti HS,
Merino J,
Lane JM,
Song Y,
Smith CE,
Tanaka T,
McKeown NM,
Tucker C,
Sun D,
Bartz TM,
Li-Gao R,
Nisa H
and 15 more — show all
Reutrakul S,
Lemaitre RN,
Alshehri TM,
de Mutsert R,
Bazzano L,
Qi L,
Knutson KL,
Psaty BM,
Mook-Kanamori DO,
Perica VB,
Neuhouser ML,
Scheer FAJL,
Rutter MK,
Garaulet M,
Saxena R
The American journal of clinical nutrition · 2019 · PMID 31190057
2 pages
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies known and novel cross-population and ancestry-specific associations as novel risk loci for Alzheimer's disease
Rajabli F,
Benchek P,
Tosto G,
Kushch N,
Sha J,
Bazemore K,
Zhu C,
Lee WP,
Haut J,
Hamilton-Nelson KL,
Wheeler NR,
Zhao Y
and 274 more — show all
Farrell JJ,
Grunin MA,
Leung YY,
Kuksa PP,
Li D,
da Fonseca EL,
Mez JB,
Palmer EL,
Pillai J,
Sherva RM,
Song YE,
Zhang X,
Ikeuchi T,
Iqbal T,
Pathak O,
Valladares O,
Reyes-Dumeyer D,
Kuzma AB,
Abner E,
Adams LD,
Adams PM,
Aguirre A,
Albert MS,
Albin RL,
Allen M,
Alvarez L,
Apostolova LG,
Arnold SE,
Asthana S,
Atwood CS,
Auerbach S,
Ayres G,
Baldwin CT,
Barber RC,
Barnes LL,
Barral S,
Beach TG,
Becker JT,
Beecham GW,
Beekly D,
Benitez BA,
Bennett D,
Bertelson J,
Bird TD,
Blacker D,
Boeve BF,
Bowen JD,
Boxer A,
Brewer J,
Burke JR,
Burns JM,
Buxbaum JD,
Cairns NJ,
Cantwell LB,
Cao C,
Carlson CS,
Carlsson CM,
Carney RM,
Carrasquillo MM,
Chasse S,
Chesselet MF,
Chin NA,
Chui HC,
Chung J,
Craft S,
Crane PK,
Cribbs DH,
Crocco EA,
Cruchaga C,
Cuccaro ML,
Cullum M,
Darby E,
Davis B,
De Jager PL,
DeCarli C,
DeToledo J,
Dick M,
Dickson DW,
Dombroski BA,
Doody RS,
Duara R,
Ertekin-Taner N,
Evans DA,
Faber KM,
Fairchild TJ,
Fallon KB,
Fardo DW,
Farlow MR,
Fernandez-Hernandez V,
Ferris S,
Friedland RP,
Foroud TM,
Frosch MP,
Fulton-Howard B,
Galasko DR,
Gamboa A,
Gearing M,
Geschwind DH,
Ghetti B,
Gilbert JR,
Go RCP,
Goate AM,
Grabowski TJ,
Graff-Radford NR,
Green RC,
Growdon JH,
Hakonarson H,
Hall J,
Hamilton RL,
Harari O,
Hardy J,
Harrell LE,
Head E,
Henderson VW,
Hernandez M,
Hohman T,
Honig LS,
Huebinger RM,
Huentelman MJ,
Hulette CM,
Hyman BT,
Hynan LS,
Ibanez L,
Jarvik GP,
Jayadev S,
Jin LW,
Johnson K,
Johnson L,
Kamboh MI,
Karydas AM,
Katz MJ,
Kauwe JS,
Kaye JA,
Keene CD,
Khaleeq A,
Kikuchi M,
Kim R,
Knebl J,
Kowall NW,
Kramer JH,
Kukull WA,
LaFerla FM,
Lah JJ,
Larson EB,
Lerner A,
Leverenz JB,
Levey AI,
Lieberman AP,
Lipton RB,
Logue M,
Lopez OL,
Lunetta KL,
Lyketsos CG,
Mains D,
Margaret FE,
Marson DC,
Martin ER,
Martiniuk F,
Mash DC,
Masliah E,
Massman P,
Masurkar A,
McCormick WC,
McCurry SM,
McDavid AN,
McDonough S,
McKee AC,
Mesulam M,
Miller BL,
Miller CA,
Miller JW,
Montine TJ,
Monuki ES,
Morris JC,
Mukherjee S,
Myers AJ,
Nguyen T,
Obisesan T,
O'Bryant S,
Olichney JM,
Ory M,
Palmer R,
Parisi JE,
Paulson HL,
Pavlik V,
Paydarfar D,
Perez V,
Peskind E,
Petersen RC,
Petrovitch H,
Pierce A,
Polk M,
Poon WW,
Potter H,
Qu L,
Quiceno M,
Quinn JF,
Raj A,
Raskind M,
Reiman EM,
Reisberg B,
Reisch JS,
Ringman JM,
Roberson ED,
Rodriguear M,
Rogaeva E,
Rosen HJ,
Rosenberg RN,
Royall DR,
Sabbagh M,
Sadovnick AD,
Sager MA,
Sano M,
Saykin AJ,
Schneider JA,
Schneider LS,
Seeley WW,
Slifer SH,
Small S,
Smith AG,
Smith JP,
Sonnen JA,
Spina S,
George-Hyslop PS,
Starks TD,
Stern RA,
Stevens AB,
Strittmatter SM,
Sultzer D,
Swerdlow RH,
Tanzi RE,
Tilson JL,
Trojanowski JQ,
Troncoso JC,
Tsolaki M,
Tsuang DW,
Van Deerlin VM,
van Eldik LJ,
Vance JM,
Vardarajan BN,
Vassar R,
Vinters HV,
Vonsattel JP,
Weintraub S,
Welsh-Bohmer KA,
Whitehead PL,
Wijsman EM,
Wilhelmsen KC,
Williams B,
Williamson J,
Wilms H,
Wingo TS,
Wisniewski T,
Woltjer RL,
Woon M,
Wright CB,
Wu CK,
Younkin SG,
Yu CE,
Yu L,
Zhu X,
Kunkle BW,
Bush WS,
Miyashita A,
Byrd GS,
Wang LS,
Farrer LA,
Haines JL,
Mayeux R,
Pericak-Vance MA,
Schellenberg GD,
Jun GR,
Reitz C,
Naj AC
Alzheimer’s Disease Genetics Consortium (ADGC)
Genome biology · 2025 · PMID 40676597 · open access
2 pages
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma
Bailey JN,
Loomis SJ,
Kang JH,
Allingham RR,
Gharahkhani P,
Khor CC,
Burdon KP,
Aschard H,
Chasman DI,
Igo RP Jr,
Hysi PG,
Glastonbury CA
and 69 more — show all
Ashley-Koch A,
Brilliant M,
Brown AA,
Budenz DL,
Buil A,
Cheng CY,
Choi H,
Christen WG,
Curhan G,
De Vivo I,
Fingert JH,
Foster PJ,
Fuchs C,
Gaasterland D,
Gaasterland T,
Hewitt AW,
Hu F,
Hunter DJ,
Khawaja AP,
Lee RK,
Li Z,
Lichter PR,
Mackey DA,
McGuffin P,
Mitchell P,
Moroi SE,
Perera SA,
Pepper KW,
Qi Q,
Realini T,
Richards JE,
Ridker PM,
Rimm E,
Ritch R,
Ritchie M,
Schuman JS,
Scott WK,
Singh K,
Sit AJ,
Song YE,
Tamimi RM,
Topouzis F,
Viswanathan AC,
Verma SS,
Vollrath D,
Wang JJ,
Weisschuh N,
Wissinger B,
Wollstein G,
Wong TY,
Yaspan BL,
Zack DJ,
Zhang K,
Study EN,
Weinreb RN,
Pericak-Vance MA,
Small K,
Hammond CJ,
Aung T,
Liu Y,
Vithana EN,
MacGregor S,
Craig JE,
Kraft P,
Howell G,
Hauser MA,
Pasquale LR,
Haines JL,
Wiggs JL
ANZRAG Consortium
Nature genetics · 2016 · PMID 26752265 · open access
1 page
Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity
Yu Y,
Zuo X,
He M,
Gao J,
Fu Y,
Qin C,
Meng L,
Wang W,
Song Y,
Cheng Y,
Zhou F,
Chen G
and 18 more — show all
Zheng X,
Wang X,
Liang B,
Zhu Z,
Fu X,
Sheng Y,
Hao J,
Liu Z,
Yan H,
Mangold E,
Ruczinski I,
Liu J,
Marazita ML,
Ludwig KU,
Beaty TH,
Zhang X,
Sun L,
Bian Z
Nature communications · 2017 · PMID 28232668 · open access
1 page
Genetic Association of a Gain-of-Function IFNGR1 Polymorphism and the Intergenic Region LNCAROD/DKK1 With Behçet's Disease
Ortiz Fernández L,
Coit P,
Yilmaz V,
Yentür SP,
Alibaz-Oner F,
Aksu K,
Erken E,
Düzgün N,
Keser G,
Cefle A,
Yazici A,
Ergen A
and 25 more — show all
Alpsoy E,
Salvarani C,
Casali B,
Kısacık B,
Kötter I,
Henes J,
Çınar M,
Schaefer A,
Nohutcu RM,
Zhernakova A,
Wijmenga C,
Takeuchi F,
Harihara S,
Kaburaki T,
Messedi M,
Song YW,
Kaşifoğlu T,
Carmona FD,
Guthridge JM,
James JA,
Martin J,
González Escribano MF,
Saruhan-Direskeneli G,
Direskeneli H,
Sawalha AH
Arthritis & rheumatology (Hoboken, N.J.) · 2021 · PMID 33393726
1 page
TMEM106B is a selective modulator of TDP-43 pathology in Alzheimer's disease
Reeves MM,
Calliari A,
Todd TW,
Maroto Cidfuentes C,
Jansen-West K,
Yue M,
Song Y,
Dunmore J,
Rawlinson B,
Engelberg-Cook E,
DeTure M,
Day GS
and 10 more — show all
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026 · PMID 42720122
1 page
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