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성함이나 학술지명, PMID로 찾아보십시오.
Ma R에 대해
53건, 그중 20건 표시.
Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes
Imamura M,
Takahashi A,
Yamauchi T,
Hara K,
Yasuda K,
Grarup N,
Zhao W,
Wang X,
Huerta-Chagoya A,
Hu C,
Moon S,
Long J
외 52명 — 모두 보기
Kwak SH,
Rasheed A,
Saxena R,
Ma RC,
Okada Y,
Iwata M,
Hosoe J,
Shojima N,
Iwasaki M,
Fujita H,
Suzuki K,
Danesh J,
Jørgensen T,
Jørgensen ME,
Witte DR,
Brandslund I,
Christensen C,
Hansen T,
Mercader JM,
Flannick J,
Moreno-Macías H,
Burtt NP,
Zhang R,
Kim YJ,
Zheng W,
Zheng W,
Singh JR,
Tam CH,
Hirose H,
Maegawa H,
Ito C,
Kaku K,
Watada H,
Tanaka Y,
Tobe K,
Kawamori R,
Kubo M,
Cho YS,
Chan JC,
Sanghera D,
Frossard P,
Park KS,
Shu XO,
Kim BJ,
Florez JC,
Tusié-Luna T,
Jia W,
Tai ES,
Pedersen O,
Saleheen D,
Maeda S,
Kadowaki T
Nature communications · 2016 · PMID 26818947 · open access
페이지 6개
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
Mahajan A,
Wessel J,
Willems SM,
Zhao W,
Robertson NR,
Chu AY,
Gan W,
Kitajima H,
Taliun D,
Rayner NW,
Guo X,
Lu Y
외 228명 — 모두 보기
Li M,
Jensen RA,
Hu Y,
Huo S,
Lohman KK,
Zhang W,
Cook JP,
Prins BP,
Flannick J,
Grarup N,
Trubetskoy VV,
Kravic J,
Kim YJ,
Rybin DV,
Yaghootkar H,
Müller-Nurasyid M,
Meidtner K,
Li-Gao R,
Varga TV,
Marten J,
Li J,
Smith AV,
An P,
Ligthart S,
Gustafsson S,
Malerba G,
Demirkan A,
Tajes JF,
Steinthorsdottir V,
Wuttke M,
Lecoeur C,
Preuss M,
Bielak LF,
Graff M,
Highland HM,
Justice AE,
Liu DJ,
Marouli E,
Peloso GM,
Warren HR,
Afaq S,
Afzal S,
Ahlqvist E,
Almgren P,
Amin N,
Bang LB,
Bertoni AG,
Bombieri C,
Bork-Jensen J,
Brandslund I,
Brody JA,
Burtt NP,
Canouil M,
Chen YI,
Cho YS,
Christensen C,
Eastwood SV,
Eckardt KU,
Fischer K,
Gambaro G,
Giedraitis V,
Grove ML,
de Haan HG,
Hackinger S,
Hai Y,
Han S,
Tybjærg-Hansen A,
Hivert MF,
Isomaa B,
Jäger S,
Jørgensen ME,
Jørgensen T,
Käräjämäki A,
Kim BJ,
Kim SS,
Koistinen HA,
Kovacs P,
Kriebel J,
Kronenberg F,
Läll K,
Lange LA,
Lee JJ,
Lehne B,
Li H,
Lin KH,
Linneberg A,
Liu CT,
Liu J,
Loh M,
Mägi R,
Mamakou V,
McKean-Cowdin R,
Nadkarni G,
Neville M,
Nielsen SF,
Ntalla I,
Peyser PA,
Rathmann W,
Rice K,
Rich SS,
Rode L,
Rolandsson O,
Schönherr S,
Selvin E,
Small KS,
Stančáková A,
Surendran P,
Taylor KD,
Teslovich TM,
Thorand B,
Thorleifsson G,
Tin A,
Tönjes A,
Varbo A,
Witte DR,
Wood AR,
Yajnik P,
Yao J,
Yengo L,
Young R,
Amouyel P,
Boeing H,
Boerwinkle E,
Bottinger EP,
Chowdhury R,
Collins FS,
Dedoussis G,
Dehghan A,
Deloukas P,
Ferrario MM,
Ferrières J,
Florez JC,
Frossard P,
Gudnason V,
Harris TB,
Heckbert SR,
Howson JMM,
Ingelsson M,
Kathiresan S,
Kee F,
Kuusisto J,
Langenberg C,
Launer LJ,
Lindgren CM,
Männistö S,
Meitinger T,
Melander O,
Mohlke KL,
Moitry M,
Morris AD,
Murray AD,
de Mutsert R,
Orho-Melander M,
Owen KR,
Perola M,
Peters A,
Province MA,
Rasheed A,
Ridker PM,
Rivadineira F,
Rosendaal FR,
Rosengren AH,
Salomaa V,
Sheu WH,
Sladek R,
Smith BH,
Strauch K,
Uitterlinden AG,
Varma R,
Willer CJ,
Blüher M,
Butterworth AS,
Chambers JC,
Chasman DI,
Danesh J,
van Duijn C,
Dupuis J,
Franco OH,
Franks PW,
Froguel P,
Grallert H,
Groop L,
Han BG,
Hansen T,
Hattersley AT,
Hayward C,
Ingelsson E,
Kardia SLR,
Karpe F,
Kooner JS,
Köttgen A,
Kuulasmaa K,
Laakso M,
Lin X,
Lind L,
Liu Y,
Loos RJF,
Marchini J,
Metspalu A,
Mook-Kanamori D,
Nordestgaard BG,
Palmer CNA,
Pankow JS,
Pedersen O,
Psaty BM,
Rauramaa R,
Sattar N,
Schulze MB,
Soranzo N,
Spector TD,
Stefansson K,
Stumvoll M,
Thorsteinsdottir U,
Tuomi T,
Tuomilehto J,
Wareham NJ,
Wilson JG,
Zeggini E,
Scott RA,
Barroso I,
Frayling TM,
Goodarzi MO,
Meigs JB,
Boehnke M,
Saleheen D,
Morris AP,
Rotter JI,
McCarthy MI
ExomeBP Consortium · MAGIC Consortium 외 컨소시엄 1곳
Nature genetics · 2018 · PMID 29632382 · open access
페이지 6개
Subtype-specific gout susceptibility loci and enrichment of selection pressure on <i>ABCG2</i> and <i>ALDH2</i> identified by subtype genome-wide meta-analyses of clinically defined gout patients
Nakayama A,
Nakatochi M,
Kawamura Y,
Yamamoto K,
Nakaoka H,
Shimizu S,
Higashino T,
Koyama T,
Hishida A,
Kuriki K,
Watanabe M,
Shimizu T
외 42명 — 모두 보기
Ooyama K,
Ooyama H,
Nagase M,
Hidaka Y,
Matsui D,
Tamura T,
Nishiyama T,
Shimanoe C,
Katsuura-Kamano S,
Takashima N,
Shirai Y,
Kawaguchi M,
Takao M,
Sugiyama R,
Takada Y,
Nakamura T,
Nakashima H,
Tsunoda M,
Danjoh I,
Hozawa A,
Hosomichi K,
Toyoda Y,
Kubota Y,
Takada T,
Suzuki H,
Stiburkova B,
Major TJ,
Merriman TR,
Kuriyama N,
Mikami H,
Takezaki T,
Matsuo K,
Suzuki S,
Hosoya T,
Kamatani Y,
Kubo M,
Ichida K,
Wakai K,
Inoue I,
Okada Y,
Shinomiya N,
Matsuo H
Japan Gout Genomics Consortium (Japan Gout)
Annals of the rheumatic diseases · 2020 · PMID 32238385 · open access
페이지 6개
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
Sotoodehnia N,
Isaacs A,
de Bakker PI,
Dörr M,
Newton-Cheh C,
Nolte IM,
van der Harst P,
Müller M,
Eijgelsheim M,
Alonso A,
Hicks AA,
Padmanabhan S
외 91명 — 모두 보기
Hayward C,
Smith AV,
Polasek O,
Giovannone S,
Fu J,
Magnani JW,
Marciante KD,
Pfeufer A,
Gharib SA,
Teumer A,
Li M,
Bis JC,
Rivadeneira F,
Aspelund T,
Köttgen A,
Johnson T,
Rice K,
Sie MP,
Wang YA,
Klopp N,
Fuchsberger C,
Wild SH,
Mateo Leach I,
Estrada K,
Völker U,
Wright AF,
Asselbergs FW,
Qu J,
Chakravarti A,
Sinner MF,
Kors JA,
Petersmann A,
Harris TB,
Soliman EZ,
Munroe PB,
Psaty BM,
Oostra BA,
Cupples LA,
Perz S,
de Boer RA,
Uitterlinden AG,
Völzke H,
Spector TD,
Liu FY,
Boerwinkle E,
Dominiczak AF,
Rotter JI,
van Herpen G,
Levy D,
Wichmann HE,
van Gilst WH,
Witteman JC,
Kroemer HK,
Kao WH,
Heckbert SR,
Meitinger T,
Hofman A,
Campbell H,
Folsom AR,
van Veldhuisen DJ,
Schwienbacher C,
O'Donnell CJ,
Volpato CB,
Caulfield MJ,
Connell JM,
Launer L,
Lu X,
Franke L,
Fehrmann RS,
te Meerman G,
Groen HJ,
Weersma RK,
van den Berg LH,
Wijmenga C,
Ophoff RA,
Navis G,
Rudan I,
Snieder H,
Wilson JF,
Pramstaller PP,
Siscovick DS,
Wang TJ,
Gudnason V,
van Duijn CM,
Felix SB,
Fishman GI,
Jamshidi Y,
Stricker BH,
Samani NJ,
Kääb S,
Arking DE
Nature genetics · 2010 · PMID 21076409 · open access
페이지 5개
Genome-wide association identifies multiple ulcerative colitis susceptibility loci
McGovern DP,
Gardet A,
Törkvist L,
Goyette P,
Essers J,
Taylor KD,
Neale BM,
Ong RT,
Lagacé C,
Li C,
Green T,
Stevens CR
외 42명 — 모두 보기
Beauchamp C,
Fleshner PR,
Carlson M,
D'Amato M,
Halfvarson J,
Hibberd ML,
Lördal M,
Padyukov L,
Andriulli A,
Colombo E,
Latiano A,
Palmieri O,
Bernard EJ,
Deslandres C,
Hommes DW,
de Jong DJ,
Stokkers PC,
Weersma RK,
Sharma Y,
Silverberg MS,
Cho JH,
Wu J,
Roeder K,
Brant SR,
Schumm LP,
Duerr RH,
Dubinsky MC,
Glazer NL,
Haritunians T,
Ippoliti A,
Melmed GY,
Siscovick DS,
Vasiliauskas EA,
Targan SR,
Annese V,
Wijmenga C,
Pettersson S,
Rotter JI,
Xavier RJ,
Daly MJ,
Rioux JD,
Seielstad M
NIDDK IBD Genetics Consortium
Nature genetics · 2010 · PMID 20228799
페이지 4개
Genome-wide association study in essential tremor identifies three new loci
Müller SH,
Girard SL,
Hopfner F,
Merner ND,
Bourassa CV,
Lorenz D,
Clark LN,
Tittmann L,
Soto-Ortolaza AI,
Klebe S,
Hallett M,
Schneider SA
외 37명 — 모두 보기
Hodgkinson CA,
Lieb W,
Wszolek ZK,
Pendziwiat M,
Lorenzo-Betancor O,
Poewe W,
Ortega-Cubero S,
Seppi K,
Rajput A,
Hussl A,
Rajput AH,
Berg D,
Dion PA,
Wurster I,
Shulman JM,
Srulijes K,
Haubenberger D,
Pastor P,
Vilariño-Güell C,
Postuma RB,
Bernard G,
Ladwig KH,
Dupré N,
Jankovic J,
Strauch K,
Panisset M,
Winkelmann J,
Testa CM,
Reischl E,
Zeuner KE,
Ross OA,
Arzberger T,
Chouinard S,
Deuschl G,
Louis ED,
Kuhlenbäumer G,
Rouleau GA
Brain : a journal of neurology · 2016 · PMID 27797806 · open access
페이지 4개
Identifying expression and DNA methylation biomarkers for lung adenocarcinoma risk in East Asia
Chen TY,
Chien LH,
Jiang SS,
Choi J,
Hung HH,
Hsiao CF,
Shi J,
Blechter B,
Breeze CE,
Chang GC,
Chen KY,
Tsai YH
외 19명 — 모두 보기
Su WC,
Huang MS,
Chen YM,
Wen YF,
Chen CY,
Wang CL,
Tsai FY,
Chen HL,
Hsieh WS,
Lin HC,
Wang LH,
Chen CJ,
Yang PC,
Chen CY,
Rothman N,
Chanock SJ,
Lan Q,
Chang IS,
Hsiung CA
Journal of the National Cancer Institute · 2026 · PMID 41581221 · open access
페이지 4개
Multiple common variants for celiac disease influencing immune gene expression
Dubois PC,
Trynka G,
Franke L,
Hunt KA,
Romanos J,
Curtotti A,
Zhernakova A,
Heap GA,
Adány R,
Aromaa A,
Bardella MT,
van den Berg LH
외 55명 — 모두 보기
Bockett NA,
de la Concha EG,
Dema B,
Fehrmann RS,
Fernández-Arquero M,
Fiatal S,
Grandone E,
Green PM,
Groen HJ,
Gwilliam R,
Houwen RH,
Hunt SE,
Kaukinen K,
Kelleher D,
Korponay-Szabo I,
Kurppa K,
MacMathuna P,
Mäki M,
Mazzilli MC,
McCann OT,
Mearin ML,
Mein CA,
Mirza MM,
Mistry V,
Mora B,
Morley KI,
Mulder CJ,
Murray JA,
Núñez C,
Oosterom E,
Ophoff RA,
Polanco I,
Peltonen L,
Platteel M,
Rybak A,
Salomaa V,
Schweizer JJ,
Sperandeo MP,
Tack GJ,
Turner G,
Veldink JH,
Verbeek WH,
Weersma RK,
Wolters VM,
Urcelay E,
Cukrowska B,
Greco L,
Neuhausen SL,
McManus R,
Barisani D,
Deloukas P,
Barrett JC,
Saavalainen P,
Wijmenga C,
van Heel DA
Nature genetics · 2010 · PMID 20190752 · open access
페이지 3개
Variants conferring risk of atrial fibrillation on chromosome 4q25
Gudbjartsson DF,
Arnar DO,
Helgadottir A,
Gretarsdottir S,
Holm H,
Sigurdsson A,
Jonasdottir A,
Baker A,
Thorleifsson G,
Kristjansson K,
Palsson A,
Blondal T
외 28명 — 모두 보기
Sulem P,
Backman VM,
Hardarson GA,
Palsdottir E,
Helgason A,
Sigurjonsdottir R,
Sverrisson JT,
Kostulas K,
Ng MC,
Baum L,
So WY,
Wong KS,
Chan JC,
Furie KL,
Greenberg SM,
Sale M,
Kelly P,
MacRae CA,
Smith EE,
Rosand J,
Hillert J,
Ma RC,
Ellinor PT,
Thorgeirsson G,
Gulcher JR,
Kong A,
Thorsteinsdottir U,
Stefansson K
Nature · 2007 · PMID 17603472
페이지 2개
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction
Gudbjartsson DF,
Bjornsdottir US,
Halapi E,
Helgadottir A,
Sulem P,
Jonsdottir GM,
Thorleifsson G,
Helgadottir H,
Steinthorsdottir V,
Stefansson H,
Williams C,
Hui J
외 61명 — 모두 보기
Beilby J,
Warrington NM,
James A,
Palmer LJ,
Koppelman GH,
Heinzmann A,
Krueger M,
Boezen HM,
Wheatley A,
Altmuller J,
Shin HD,
Uh ST,
Cheong HS,
Jonsdottir B,
Gislason D,
Park CS,
Rasmussen LM,
Porsbjerg C,
Hansen JW,
Backer V,
Werge T,
Janson C,
Jönsson UB,
Ng MC,
Chan J,
So WY,
Ma R,
Shah SH,
Granger CB,
Quyyumi AA,
Levey AI,
Vaccarino V,
Reilly MP,
Rader DJ,
Williams MJ,
van Rij AM,
Jones GT,
Trabetti E,
Malerba G,
Pignatti PF,
Boner A,
Pescollderungg L,
Girelli D,
Olivieri O,
Martinelli N,
Ludviksson BR,
Ludviksdottir D,
Eyjolfsson GI,
Arnar D,
Thorgeirsson G,
Deichmann K,
Thompson PJ,
Wjst M,
Hall IP,
Postma DS,
Gislason T,
Gulcher J,
Kong A,
Jonsdottir I,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2009 · PMID 19198610
페이지 2개
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk
Chubb D,
Weinhold N,
Broderick P,
Chen B,
Johnson DC,
Försti A,
Vijayakrishnan J,
Migliorini G,
Dobbins SE,
Holroyd A,
Hose D,
Walker BA
외 23명 — 모두 보기
Davies FE,
Gregory WA,
Jackson GH,
Irving JA,
Pratt G,
Fegan C,
Fenton JA,
Neben K,
Hoffmann P,
Nöthen MM,
Mühleisen TW,
Eisele L,
Ross FM,
Straka C,
Einsele H,
Langer C,
Dörner E,
Allan JM,
Jauch A,
Morgan GJ,
Hemminki K,
Houlston RS,
Goldschmidt H
Nature genetics · 2013 · PMID 23955597 · open access
페이지 2개
Genome-wide association scan in north Indians reveals three novel HLA-independent risk loci for ulcerative colitis
Juyal G,
Negi S,
Sood A,
Gupta A,
Prasad P,
Senapati S,
Zaneveld J,
Singh S,
Midha V,
van Sommeren S,
Weersma RK,
Ott J
외 3명 — 모두 보기
Gut · 2015 · PMID 24837172
페이지 2개
A meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locus
Cozen W,
Timofeeva MN,
Li D,
Diepstra A,
Hazelett D,
Delahaye-Sourdeix M,
Edlund CK,
Franke L,
Rostgaard K,
Van Den Berg DJ,
Cortessis VK,
Smedby KE
외 55명 — 모두 보기
Glaser SL,
Westra HJ,
Robison LL,
Mack TM,
Ghesquieres H,
Hwang AE,
Nieters A,
de Sanjose S,
Lightfoot T,
Becker N,
Maynadie M,
Foretova L,
Roman E,
Benavente Y,
Rand KA,
Nathwani BN,
Glimelius B,
Staines A,
Boffetta P,
Link BK,
Kiemeney L,
Ansell SM,
Bhatia S,
Strong LC,
Galan P,
Vatten L,
Habermann TM,
Duell EJ,
Lake A,
Veenstra RN,
Visser L,
Liu Y,
Urayama KY,
Montgomery D,
Gaborieau V,
Weiss LM,
Byrnes G,
Lathrop M,
Cocco P,
Best T,
Skol AD,
Adami HO,
Melbye M,
Cerhan JR,
Gallagher A,
Taylor GM,
Slager SL,
Brennan P,
Coetzee GA,
Conti DV,
Onel K,
Jarrett RF,
Hjalgrim H,
van den Berg A,
McKay JD
Nature communications · 2014 · PMID 24920014 · open access
페이지 2개
Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk
Chang X,
Zhao Y,
Hou C,
Glessner J,
McDaniel L,
Diamond MA,
Thomas K,
Li J,
Wei Z,
Liu Y,
Guo Y,
Mentch FD
외 9명 — 모두 보기
Nature communications · 2017 · PMID 28924153 · open access
페이지 2개
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Flannick J,
Mercader JM,
Fuchsberger C,
Udler MS,
Mahajan A,
Wessel J,
Teslovich TM,
Caulkins L,
Koesterer R,
Barajas-Olmos F,
Blackwell TW,
Boerwinkle E
외 152명 — 모두 보기
Brody JA,
Centeno-Cruz F,
Chen L,
Chen S,
Contreras-Cubas C,
Córdova E,
Correa A,
Cortes M,
DeFronzo RA,
Dolan L,
Drews KL,
Elliott A,
Floyd JS,
Gabriel S,
Garay-Sevilla ME,
García-Ortiz H,
Gross M,
Han S,
Heard-Costa NL,
Jackson AU,
Jørgensen ME,
Kang HM,
Kelsey M,
Kim BJ,
Koistinen HA,
Kuusisto J,
Leader JB,
Linneberg A,
Liu CT,
Liu J,
Lyssenko V,
Manning AK,
Marcketta A,
Malacara-Hernandez JM,
Martínez-Hernández A,
Matsuo K,
Mayer-Davis E,
Mendoza-Caamal E,
Mohlke KL,
Morrison AC,
Ndungu A,
Ng MCY,
O'Dushlaine C,
Payne AJ,
Pihoker C,
Post WS,
Preuss M,
Psaty BM,
Vasan RS,
Rayner NW,
Reiner AP,
Revilla-Monsalve C,
Robertson NR,
Santoro N,
Schurmann C,
So WY,
Soberón X,
Stringham HM,
Strom TM,
Tam CHT,
Thameem F,
Tomlinson B,
Torres JM,
Tracy RP,
van Dam RM,
Vujkovic M,
Wang S,
Welch RP,
Witte DR,
Wong TY,
Atzmon G,
Barzilai N,
Blangero J,
Bonnycastle LL,
Bowden DW,
Chambers JC,
Chan E,
Cheng CY,
Cho YS,
Collins FS,
de Vries PS,
Duggirala R,
Glaser B,
Gonzalez C,
Gonzalez ME,
Groop L,
Kooner JS,
Kwak SH,
Laakso M,
Lehman DM,
Nilsson P,
Spector TD,
Tai ES,
Tuomi T,
Tuomilehto J,
Wilson JG,
Aguilar-Salinas CA,
Bottinger E,
Burke B,
Carey DJ,
Chan JCN,
Dupuis J,
Frossard P,
Heckbert SR,
Hwang MY,
Kim YJ,
Kirchner HL,
Lee JY,
Lee J,
Loos RJF,
Ma RCW,
Morris AD,
O'Donnell CJ,
Palmer CNA,
Pankow J,
Park KS,
Rasheed A,
Saleheen D,
Sim X,
Small KS,
Teo YY,
Haiman C,
Hanis CL,
Henderson BE,
Orozco L,
Tusié-Luna T,
Dewey FE,
Baras A,
Gieger C,
Meitinger T,
Strauch K,
Lange L,
Grarup N,
Hansen T,
Pedersen O,
Zeitler P,
Dabelea D,
Abecasis G,
Bell GI,
Cox NJ,
Seielstad M,
Sladek R,
Meigs JB,
Rich SS,
Rotter JI,
Altshuler D,
Burtt NP,
Scott LJ,
Morris AP,
Florez JC,
McCarthy MI,
Boehnke M
Broad Genomics Platform · DiscovEHR Collaboration 외 컨소시엄 8곳
Nature · 2019 · PMID 31118516 · open access
페이지 2개
Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project
Lopera-Maya EA,
Kurilshikov A,
van der Graaf A,
Hu S,
Andreu-Sánchez S,
Chen L,
Vila AV,
Gacesa R,
Sinha T,
Collij V,
Klaassen MAY,
Bolte LA
외 9명 — 모두 보기
LifeLines Cohort Study
Nature genetics · 2022 · PMID 35115690
페이지 2개
Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects
Krohn L,
Heilbron K,
Blauwendraat C,
Reynolds RH,
Yu E,
Senkevich K,
Rudakou U,
Estiar MA,
Gustavsson EK,
Brolin K,
Ruskey JA,
Freeman K
외 46명 — 모두 보기
Asayesh F,
Chia R,
Arnulf I,
Hu MTM,
Montplaisir JY,
Gagnon JF,
Desautels A,
Dauvilliers Y,
Gigli GL,
Valente M,
Janes F,
Bernardini A,
Högl B,
Stefani A,
Ibrahim A,
Šonka K,
Kemlink D,
Oertel W,
Janzen A,
Plazzi G,
Biscarini F,
Antelmi E,
Figorilli M,
Puligheddu M,
Mollenhauer B,
Trenkwalder C,
Sixel-Döring F,
Cochen De Cock V,
Monaca CC,
Heidbreder A,
Ferini-Strambi L,
Dijkstra F,
Viaene M,
Abril B,
Boeve BF,
Scholz SW,
Ryten M,
Bandres-Ciga S,
Noyce A,
Cannon P,
Pihlstrøm L,
Nalls MA,
Singleton AB,
Rouleau GA,
Postuma RB,
Gan-Or Z
23andMe Research Team
Nature communications · 2022 · PMID 36470867 · open access
페이지 2개
Human Leukocyte Antigen Signatures as Pathophysiological Discriminants of Microscopic Colitis Subtypes
Zheng T,
Roda G,
Zabana Y,
Escudero-Hernández C,
Liu X,
Chen Y,
Camargo Tavares L,
Bonfiglio F,
Mellander MR,
Janczewska I,
Vigren L,
Sjöberg K
외 27명 — 모두 보기
Ohlsson B,
Almer S,
Halfvarson J,
Miehlke S,
Madisch A,
Lieb W,
Kupčinskas J,
Weersma RK,
Bujanda L,
Julià A,
Marsal S,
Esteve M,
Guagnozzi D,
Fernández-Bañares F,
Ferrer C,
Peter I,
Ludvigsson JF,
Pardi D,
Verhaegh B,
Jonkers D,
Pierik M,
Münch A,
Franke A,
Bresso F,
Khalili H,
Colombel JF,
D'Amato M
MC-Europe GETECCU GWAS group
Journal of Crohn's & colitis · 2024 · PMID 37768647
페이지 2개
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