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성함이나 학술지명, PMID로 찾아보십시오.
van den Berg L에 대해
10건.
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
Anderson CA,
Boucher G,
Lees CW,
Franke A,
D'Amato M,
Taylor KD,
Lee JC,
Goyette P,
Imielinski M,
Latiano A,
Lagacé C,
Scott R
외 101명 — 모두 보기
Amininejad L,
Bumpstead S,
Baidoo L,
Baldassano RN,
Barclay M,
Bayless TM,
Brand S,
Büning C,
Colombel JF,
Denson LA,
De Vos M,
Dubinsky M,
Edwards C,
Ellinghaus D,
Fehrmann RS,
Floyd JA,
Florin T,
Franchimont D,
Franke L,
Georges M,
Glas J,
Glazer NL,
Guthery SL,
Haritunians T,
Hayward NK,
Hugot JP,
Jobin G,
Laukens D,
Lawrance I,
Lémann M,
Levine A,
Libioulle C,
Louis E,
McGovern DP,
Milla M,
Montgomery GW,
Morley KI,
Mowat C,
Ng A,
Newman W,
Ophoff RA,
Papi L,
Palmieri O,
Peyrin-Biroulet L,
Panés J,
Phillips A,
Prescott NJ,
Proctor DD,
Roberts R,
Russell R,
Rutgeerts P,
Sanderson J,
Sans M,
Schumm P,
Seibold F,
Sharma Y,
Simms LA,
Seielstad M,
Steinhart AH,
Targan SR,
van den Berg LH,
Vatn M,
Verspaget H,
Walters T,
Wijmenga C,
Wilson DC,
Westra HJ,
Xavier RJ,
Zhao ZZ,
Ponsioen CY,
Andersen V,
Torkvist L,
Gazouli M,
Anagnou NP,
Karlsen TH,
Kupcinskas L,
Sventoraityte J,
Mansfield JC,
Kugathasan S,
Silverberg MS,
Halfvarson J,
Rotter JI,
Mathew CG,
Griffiths AM,
Gearry R,
Ahmad T,
Brant SR,
Chamaillard M,
Satsangi J,
Cho JH,
Schreiber S,
Daly MJ,
Barrett JC,
Parkes M,
Annese V,
Hakonarson H,
Radford-Smith G,
Duerr RH,
Vermeire S,
Weersma RK,
Rioux JD
Nature genetics · 2011 · PMID 21297633 · open access
페이지 12개+
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
Bakker MK,
van der Spek RAA,
van Rheenen W,
Morel S,
Bourcier R,
Hostettler IC,
Alg VS,
van Eijk KR,
Koido M,
Akiyama M,
Terao C,
Matsuda K
외 62명 — 모두 보기
Walters RG,
Lin K,
Li L,
Millwood IY,
Chen Z,
Rouleau GA,
Zhou S,
Rannikmäe K,
Sudlow CLM,
Houlden H,
van den Berg LH,
Dina C,
Naggara O,
Gentric JC,
Shotar E,
Eugène F,
Desal H,
Winsvold BS,
Børte S,
Johnsen MB,
Brumpton BM,
Sandvei MS,
Willer CJ,
Hveem K,
Zwart JA,
Verschuren WMM,
Friedrich CM,
Hirsch S,
Schilling S,
Dauvillier J,
Martin O,
Jones GT,
Bown MJ,
Ko NU,
Kim H,
Coleman JRI,
Breen G,
Zaroff JG,
Klijn CJM,
Malik R,
Dichgans M,
Sargurupremraj M,
Tatlisumak T,
Amouyel P,
Debette S,
Rinkel GJE,
Worrall BB,
Pera J,
Slowik A,
Gaál-Paavola EI,
Niemelä M,
Jääskeläinen JE,
von Und Zu Fraunberg M,
Lindgren A,
Broderick JP,
Werring DJ,
Woo D,
Redon R,
Bijlenga P,
Kamatani Y,
Veldink JH,
Ruigrok YM
HUNT All-In Stroke · China Kadoorie Biobank Collaborative Group 외 컨소시엄 5곳
Nature genetics · 2020 · PMID 33199917
페이지 6개
Genome-wide association study of intracranial aneurysm identifies three new risk loci
Yasuno K,
Bilguvar K,
Bijlenga P,
Low SK,
Krischek B,
Auburger G,
Simon M,
Krex D,
Arlier Z,
Nayak N,
Ruigrok YM,
Niemelä M
외 57명 — 모두 보기
Tajima A,
von und zu Fraunberg M,
Dóczi T,
Wirjatijasa F,
Hata A,
Blasco J,
Oszvald A,
Kasuya H,
Zilani G,
Schoch B,
Singh P,
Stüer C,
Risselada R,
Beck J,
Sola T,
Ricciardi F,
Aromaa A,
Illig T,
Schreiber S,
van Duijn CM,
van den Berg LH,
Perret C,
Proust C,
Roder C,
Ozturk AK,
Gaál E,
Berg D,
Geisen C,
Friedrich CM,
Summers P,
Frangi AF,
State MW,
Wichmann HE,
Breteler MM,
Wijmenga C,
Mane S,
Peltonen L,
Elio V,
Sturkenboom MC,
Lawford P,
Byrne J,
Macho J,
Sandalcioglu EI,
Meyer B,
Raabe A,
Steinmetz H,
Rüfenacht D,
Jääskeläinen JE,
Hernesniemi J,
Rinkel GJ,
Zembutsu H,
Inoue I,
Palotie A,
Cambien F,
Nakamura Y,
Lifton RP,
Günel M
Nature genetics · 2010 · PMID 20364137 · open access
페이지 5개
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 analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
Barc J,
Tadros R,
Glinge C,
Chiang DY,
Jouni M,
Simonet F,
Jurgens SJ,
Baudic M,
Nicastro M,
Potet F,
Offerhaus JA,
Walsh R
외 134명 — 모두 보기
Choi SH,
Verkerk AO,
Mizusawa Y,
Anys S,
Minois D,
Arnaud M,
Duchateau J,
Wijeyeratne YD,
Muir A,
Papadakis M,
Castelletti S,
Torchio M,
Ortuño CG,
Lacunza J,
Giachino DF,
Cerrato N,
Martins RP,
Campuzano O,
Van Dooren S,
Thollet A,
Kyndt F,
Mazzanti A,
Clémenty N,
Bisson A,
Corveleyn A,
Stallmeyer B,
Dittmann S,
Saenen J,
Noël A,
Honarbakhsh S,
Rudic B,
Marzak H,
Rowe MK,
Federspiel C,
Le Page S,
Placide L,
Milhem A,
Barajas-Martinez H,
Beckmann BM,
Krapels IP,
Steinfurt J,
Winkel BG,
Jabbari R,
Shoemaker MB,
Boukens BJ,
Škorić-Milosavljević D,
Bikker H,
Manevy F,
Lichtner P,
Ribasés M,
Meitinger T,
Müller-Nurasyid M,
Veldink JH,
van den Berg LH,
Van Damme P,
Cusi D,
Lanzani C,
Rigade S,
Charpentier E,
Baron E,
Bonnaud S,
Lecointe S,
Donnart A,
Le Marec H,
Chatel S,
Karakachoff M,
Bézieau S,
London B,
Tfelt-Hansen J,
Roden D,
Odening KE,
Cerrone M,
Chinitz LA,
Volders PG,
van de Berg MP,
Laurent G,
Faivre L,
Antzelevitch C,
Kääb S,
Arnaout AA,
Dupuis JM,
Pasquie JL,
Billon O,
Roberts JD,
Jesel L,
Borggrefe M,
Lambiase PD,
Mansourati J,
Loeys B,
Leenhardt A,
Guicheney P,
Maury P,
Schulze-Bahr E,
Robyns T,
Breckpot J,
Babuty D,
Priori SG,
Napolitano C,
de Asmundis C,
Brugada P,
Brugada R,
Arbelo E,
Brugada J,
Mabo P,
Behar N,
Giustetto C,
Molina MS,
Gimeno JR,
Hasdemir C,
Schwartz PJ,
Crotti L,
McKeown PP,
Sharma S,
Behr ER,
Haissaguerre M,
Sacher F,
Rooryck C,
Tan HL,
Remme CA,
Postema PG,
Delmar M,
Ellinor PT,
Lubitz SA,
Gourraud JB,
Tanck MW,
George AL Jr,
MacRae CA,
Burridge PW,
Dina C,
Probst V,
Wilde AA,
Schott JJ,
Redon R,
Bezzina CR
KORA-Study Group · Nantes Referral Center for inherited cardiac arrhythmia
Nature genetics · 2022 · PMID 35210625
페이지 5개
Susceptibility loci for intracranial aneurysm in European and Japanese populations
Bilguvar K,
Yasuno K,
Niemelä M,
Ruigrok YM,
von Und Zu Fraunberg M,
van Duijn CM,
van den Berg LH,
Mane S,
Mason CE,
Choi M,
Gaál E,
Bayri Y
외 21명 — 모두 보기
Kolb L,
Arlier Z,
Ravuri S,
Ronkainen A,
Tajima A,
Laakso A,
Hata A,
Kasuya H,
Koivisto T,
Rinne J,
Ohman J,
Breteler MM,
Wijmenga C,
State MW,
Rinkel GJ,
Hernesniemi J,
Jääskeläinen JE,
Palotie A,
Inoue I,
Lifton RP,
Günel M
Nature genetics · 2008 · PMID 18997786
페이지 3개
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
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
van Rheenen W,
van der Spek RAA,
Bakker MK,
van Vugt JJFA,
Hop PJ,
Zwamborn RAJ,
de Klein N,
Westra HJ,
Bakker OB,
Deelen P,
Shireby G,
Hannon E
외 180명 — 모두 보기
Moisse M,
Baird D,
Restuadi R,
Dolzhenko E,
Dekker AM,
Gawor K,
Westeneng HJ,
Tazelaar GHP,
van Eijk KR,
Kooyman M,
Byrne RP,
Doherty M,
Heverin M,
Al Khleifat A,
Iacoangeli A,
Shatunov A,
Ticozzi N,
Cooper-Knock J,
Smith BN,
Gromicho M,
Chandran S,
Pal S,
Morrison KE,
Shaw PJ,
Hardy J,
Orrell RW,
Sendtner M,
Meyer T,
Başak N,
van der Kooi AJ,
Ratti A,
Fogh I,
Gellera C,
Lauria G,
Corti S,
Cereda C,
Sproviero D,
D'Alfonso S,
Sorarù G,
Siciliano G,
Filosto M,
Padovani A,
Chiò A,
Calvo A,
Moglia C,
Brunetti M,
Canosa A,
Grassano M,
Beghi E,
Pupillo E,
Logroscino G,
Nefussy B,
Osmanovic A,
Nordin A,
Lerner Y,
Zabari M,
Gotkine M,
Baloh RH,
Bell S,
Vourc'h P,
Corcia P,
Couratier P,
Millecamps S,
Meininger V,
Salachas F,
Mora Pardina JS,
Assialioui A,
Rojas-García R,
Dion PA,
Ross JP,
Ludolph AC,
Weishaupt JH,
Brenner D,
Freischmidt A,
Bensimon G,
Brice A,
Durr A,
Payan CAM,
Saker-Delye S,
Wood NW,
Topp S,
Rademakers R,
Tittmann L,
Lieb W,
Franke A,
Ripke S,
Braun A,
Kraft J,
Whiteman DC,
Olsen CM,
Uitterlinden AG,
Hofman A,
Rietschel M,
Cichon S,
Nöthen MM,
Amouyel P,
Traynor BJ,
Singleton AB,
Mitne Neto M,
Cauchi RJ,
Ophoff RA,
Wiedau-Pazos M,
Lomen-Hoerth C,
van Deerlin VM,
Grosskreutz J,
Roediger A,
Gaur N,
Jörk A,
Barthel T,
Theele E,
Ilse B,
Stubendorff B,
Witte OW,
Steinbach R,
Hübner CA,
Graff C,
Brylev L,
Fominykh V,
Demeshonok V,
Ataulina A,
Rogelj B,
Koritnik B,
Zidar J,
Ravnik-Glavač M,
Glavač D,
Stević Z,
Drory V,
Povedano M,
Blair IP,
Kiernan MC,
Benyamin B,
Henderson RD,
Furlong S,
Mathers S,
McCombe PA,
Needham M,
Ngo ST,
Nicholson GA,
Pamphlett R,
Rowe DB,
Steyn FJ,
Williams KL,
Mather KA,
Sachdev PS,
Henders AK,
Wallace L,
de Carvalho M,
Pinto S,
Petri S,
Weber M,
Rouleau GA,
Silani V,
Curtis CJ,
Breen G,
Glass JD,
Brown RH Jr,
Landers JE,
Shaw CE,
Andersen PM,
Groen EJN,
van Es MA,
Pasterkamp RJ,
Fan D,
Garton FC,
McRae AF,
Davey Smith G,
Gaunt TR,
Eberle MA,
Mill J,
McLaughlin RL,
Hardiman O,
Kenna KP,
Wray NR,
Tsai E,
Runz H,
Franke L,
Al-Chalabi A,
Van Damme P,
van den Berg LH,
Veldink JH
SLALOM Consortium · PARALS Consortium 외 컨소시엄 2곳
Nature genetics · 2021 · PMID 34873335 · open access
페이지 3개
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis
Fogh I,
Ratti A,
Gellera C,
Lin K,
Tiloca C,
Moskvina V,
Corrado L,
Sorarù G,
Cereda C,
Corti S,
Gentilini D,
Calini D
외 53명 — 모두 보기
Castellotti B,
Mazzini L,
Querin G,
Gagliardi S,
Del Bo R,
Conforti FL,
Siciliano G,
Inghilleri M,
Saccà F,
Bongioanni P,
Penco S,
Corbo M,
Sorbi S,
Filosto M,
Ferlini A,
Di Blasio AM,
Signorini S,
Shatunov A,
Jones A,
Shaw PJ,
Morrison KE,
Farmer AE,
Van Damme P,
Robberecht W,
Chiò A,
Traynor BJ,
Sendtner M,
Melki J,
Meininger V,
Hardiman O,
Andersen PM,
Leigh NP,
Glass JD,
Overste D,
Diekstra FP,
Veldink JH,
van Es MA,
Shaw CE,
Weale ME,
Lewis CM,
Williams J,
Brown RH,
Landers JE,
Ticozzi N,
Ceroni M,
Pegoraro E,
Comi GP,
D'Alfonso S,
van den Berg LH,
Taroni F,
Al-Chalabi A,
Powell J,
Silani V
SLAGEN Consortium and Collaborators
Human molecular genetics · 2014 · PMID 24256812
페이지 2개
Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci
Tanskanen T,
van den Berg L,
Välimäki N,
Aavikko M,
Ness-Jensen E,
Hveem K,
Wettergren Y,
Bexe Lindskog E,
Tõnisson N,
Metspalu A,
Silander K,
Orlando G
외 48명 — 모두 보기
Law PJ,
Tuupanen S,
Gylfe AE,
Hänninen UA,
Cajuso T,
Kondelin J,
Sarin AP,
Pukkala E,
Jousilahti P,
Salomaa V,
Ripatti S,
Palotie A,
Järvinen H,
Renkonen-Sinisalo L,
Lepistö A,
Böhm J,
Mecklin JP,
Al-Tassan NA,
Palles C,
Martin L,
Barclay E,
Tenesa A,
Farrington SM,
Timofeeva MN,
Meyer BF,
Wakil SM,
Campbell H,
Smith CG,
Idziaszczyk S,
Maughan TS,
Kaplan R,
Kerr R,
Kerr D,
Buchanan DD,
Win AK,
Hopper J,
Jenkins MA,
Newcomb PA,
Gallinger S,
Conti D,
Schumacher FR,
Casey G,
Cheadle JP,
Dunlop MG,
Tomlinson IP,
Houlston RS,
Palin K,
Aaltonen LA
International journal of cancer · 2018 · PMID 28960316
페이지 1개
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보다 지적을 받는 편이 낫습니다.
제 논문이 없습니다. 탈락시킨 것입니까?
아닙니다. 이 카탈로그는 작은 팀이 읽을 수 있었던 것으로 모은 것이고, 유럽계 조상 코호트
바깥이 가장 얇습니다. 논문이 없는 것은 아직 아무도 거기까지 가지 못했기 때문이지 검토해서
제외한 것이 아닙니다.
어떤 페이지가 그 논문 위에 서 있는지 볼 수 있습니까?
각 줄에 최대 여섯 개까지 표시되며 각각 링크되어 있습니다. 줄 옆의 숫자는 그 논문을
인용하는 페이지가 모두 몇 개인지입니다.
얼마나 자주 갱신됩니까?
페이지들에서 매시간 다시 만들어집니다. 어떤 페이지가 그 논문 위에 서기 시작하면 그
순간 나타나고 그만두면 사라집니다. 따로 관리하는 목록이 없기 때문인데, 인용은 그 주장을
하는 페이지에 붙어 있어야 하기 때문입니다.