연구자에게
내 논문이 여기 있나요?
논문 2,661편이 이 사이트를 떠받치고 있습니다. 모든 변이·질환 페이지가
자기가 어떤 연구로부터 쓰였는지 밝히며, 이것이 그 목록을 페이지들에서 모은 것입니다.
성함이나 학술지명, PMID로 찾아보십시오.
Houwing-Duistermaat JJ에 대해
6건.
Defining the role of common variation in the genomic and biological architecture of adult human height
Wood AR,
Esko T,
Yang J,
Vedantam S,
Pers TH,
Gustafsson S,
Chu AY,
Estrada K,
Luan J,
Kutalik Z,
Amin N,
Buchkovich ML
외 433명 — 모두 보기
Croteau-Chonka DC,
Day FR,
Duan Y,
Fall T,
Fehrmann R,
Ferreira T,
Jackson AU,
Karjalainen J,
Lo KS,
Locke AE,
Mägi R,
Mihailov E,
Porcu E,
Randall JC,
Scherag A,
Vinkhuyzen AA,
Westra HJ,
Winkler TW,
Workalemahu T,
Zhao JH,
Absher D,
Albrecht E,
Anderson D,
Baron J,
Beekman M,
Demirkan A,
Ehret GB,
Feenstra B,
Feitosa MF,
Fischer K,
Fraser RM,
Goel A,
Gong J,
Justice AE,
Kanoni S,
Kleber ME,
Kristiansson K,
Lim U,
Lotay V,
Lui JC,
Mangino M,
Mateo Leach I,
Medina-Gomez C,
Nalls MA,
Nyholt DR,
Palmer CD,
Pasko D,
Pechlivanis S,
Prokopenko I,
Ried JS,
Ripke S,
Shungin D,
Stancáková A,
Strawbridge RJ,
Sung YJ,
Tanaka T,
Teumer A,
Trompet S,
van der Laan SW,
van Setten J,
Van Vliet-Ostaptchouk JV,
Wang Z,
Yengo L,
Zhang W,
Afzal U,
Arnlöv J,
Arscott GM,
Bandinelli S,
Barrett A,
Bellis C,
Bennett AJ,
Berne C,
Blüher M,
Bolton JL,
Böttcher Y,
Boyd HA,
Bruinenberg M,
Buckley BM,
Buyske S,
Caspersen IH,
Chines PS,
Clarke R,
Claudi-Boehm S,
Cooper M,
Daw EW,
De Jong PA,
Deelen J,
Delgado G,
Denny JC,
Dhonukshe-Rutten R,
Dimitriou M,
Doney AS,
Dörr M,
Eklund N,
Eury E,
Folkersen L,
Garcia ME,
Geller F,
Giedraitis V,
Go AS,
Grallert H,
Grammer TB,
Gräßler J,
Grönberg H,
de Groot LC,
Groves CJ,
Haessler J,
Hall P,
Haller T,
Hallmans G,
Hannemann A,
Hartman CA,
Hassinen M,
Hayward C,
Heard-Costa NL,
Helmer Q,
Hemani G,
Henders AK,
Hillege HL,
Hlatky MA,
Hoffmann W,
Hoffmann P,
Holmen O,
Houwing-Duistermaat JJ,
Illig T,
Isaacs A,
James AL,
Jeff J,
Johansen B,
Johansson Å,
Jolley J,
Juliusdottir T,
Junttila J,
Kho AN,
Kinnunen L,
Klopp N,
Kocher T,
Kratzer W,
Lichtner P,
Lind L,
Lindström J,
Lobbens S,
Lorentzon M,
Lu Y,
Lyssenko V,
Magnusson PK,
Mahajan A,
Maillard M,
McArdle WL,
McKenzie CA,
McLachlan S,
McLaren PJ,
Menni C,
Merger S,
Milani L,
Moayyeri A,
Monda KL,
Morken MA,
Müller G,
Müller-Nurasyid M,
Musk AW,
Narisu N,
Nauck M,
Nolte IM,
Nöthen MM,
Oozageer L,
Pilz S,
Rayner NW,
Renstrom F,
Robertson NR,
Rose LM,
Roussel R,
Sanna S,
Scharnagl H,
Scholtens S,
Schumacher FR,
Schunkert H,
Scott RA,
Sehmi J,
Seufferlein T,
Shi J,
Silventoinen K,
Smit JH,
Smith AV,
Smolonska J,
Stanton AV,
Stirrups K,
Stott DJ,
Stringham HM,
Sundström J,
Swertz MA,
Syvänen AC,
Tayo BO,
Thorleifsson G,
Tyrer JP,
van Dijk S,
van Schoor NM,
van der Velde N,
van Heemst D,
van Oort FV,
Vermeulen SH,
Verweij N,
Vonk JM,
Waite LL,
Waldenberger M,
Wennauer R,
Wilkens LR,
Willenborg C,
Wilsgaard T,
Wojczynski MK,
Wong A,
Wright AF,
Zhang Q,
Arveiler D,
Bakker SJ,
Beilby J,
Bergman RN,
Bergmann S,
Biffar R,
Blangero J,
Boomsma DI,
Bornstein SR,
Bovet P,
Brambilla P,
Brown MJ,
Campbell H,
Caulfield MJ,
Chakravarti A,
Collins R,
Collins FS,
Crawford DC,
Cupples LA,
Danesh J,
de Faire U,
den Ruijter HM,
Erbel R,
Erdmann J,
Eriksson JG,
Farrall M,
Ferrannini E,
Ferrières J,
Ford I,
Forouhi NG,
Forrester T,
Gansevoort RT,
Gejman PV,
Gieger C,
Golay A,
Gottesman O,
Gudnason V,
Gyllensten U,
Haas DW,
Hall AS,
Harris TB,
Hattersley AT,
Heath AC,
Hengstenberg C,
Hicks AA,
Hindorff LA,
Hingorani AD,
Hofman A,
Hovingh GK,
Humphries SE,
Hunt SC,
Hypponen E,
Jacobs KB,
Jarvelin MR,
Jousilahti P,
Jula AM,
Kaprio J,
Kastelein JJ,
Kayser M,
Kee F,
Keinanen-Kiukaanniemi SM,
Kiemeney LA,
Kooner JS,
Kooperberg C,
Koskinen S,
Kovacs P,
Kraja AT,
Kumari M,
Kuusisto J,
Lakka TA,
Langenberg C,
Le Marchand L,
Lehtimäki T,
Lupoli S,
Madden PA,
Männistö S,
Manunta P,
Marette A,
Matise TC,
McKnight B,
Meitinger T,
Moll FL,
Montgomery GW,
Morris AD,
Morris AP,
Murray JC,
Nelis M,
Ohlsson C,
Oldehinkel AJ,
Ong KK,
Ouwehand WH,
Pasterkamp G,
Peters A,
Pramstaller PP,
Price JF,
Qi L,
Raitakari OT,
Rankinen T,
Rao DC,
Rice TK,
Ritchie M,
Rudan I,
Salomaa V,
Samani NJ,
Saramies J,
Sarzynski MA,
Schwarz PE,
Sebert S,
Sever P,
Shuldiner AR,
Sinisalo J,
Steinthorsdottir V,
Stolk RP,
Tardif JC,
Tönjes A,
Tremblay A,
Tremoli E,
Virtamo J,
Vohl MC,
Amouyel P,
Asselbergs FW,
Assimes TL,
Bochud M,
Boehm BO,
Boerwinkle E,
Bottinger EP,
Bouchard C,
Cauchi S,
Chambers JC,
Chanock SJ,
Cooper RS,
de Bakker PI,
Dedoussis G,
Ferrucci L,
Franks PW,
Froguel P,
Groop LC,
Haiman CA,
Hamsten A,
Hayes MG,
Hui J,
Hunter DJ,
Hveem K,
Jukema JW,
Kaplan RC,
Kivimaki M,
Kuh D,
Laakso M,
Liu Y,
Martin NG,
März W,
Melbye M,
Moebus S,
Munroe PB,
Njølstad I,
Oostra BA,
Palmer CN,
Pedersen NL,
Perola M,
Pérusse L,
Peters U,
Powell JE,
Power C,
Quertermous T,
Rauramaa R,
Reinmaa E,
Ridker PM,
Rivadeneira F,
Rotter JI,
Saaristo TE,
Saleheen D,
Schlessinger D,
Slagboom PE,
Snieder H,
Spector TD,
Strauch K,
Stumvoll M,
Tuomilehto J,
Uusitupa M,
van der Harst P,
Völzke H,
Walker M,
Wareham NJ,
Watkins H,
Wichmann HE,
Wilson JF,
Zanen P,
Deloukas P,
Heid IM,
Lindgren CM,
Mohlke KL,
Speliotes EK,
Thorsteinsdottir U,
Barroso I,
Fox CS,
North KE,
Strachan DP,
Beckmann JS,
Berndt SI,
Boehnke M,
Borecki IB,
McCarthy MI,
Metspalu A,
Stefansson K,
Uitterlinden AG,
van Duijn CM,
Franke L,
Willer CJ,
Price AL,
Lettre G,
Loos RJ,
Weedon MN,
Ingelsson E,
O'Connell JR,
Abecasis GR,
Chasman DI,
Goddard ME,
Visscher PM,
Hirschhorn JN,
Frayling TM
Electronic Medical Records and Genomics (eMEMERGEGE) Consortium · MIGen Consortium 외 컨소시엄 2곳
Nature genetics · 2014 · PMID 25282103 · open access
페이지 12개+
The impact of low-frequency and rare variants on lipid levels
Surakka I,
Horikoshi M,
Mägi R,
Sarin AP,
Mahajan A,
Lagou V,
Marullo L,
Ferreira T,
Miraglio B,
Timonen S,
Kettunen J,
Pirinen M
외 74명 — 모두 보기
Karjalainen J,
Thorleifsson G,
Hägg S,
Hottenga JJ,
Isaacs A,
Ladenvall C,
Beekman M,
Esko T,
Ried JS,
Nelson CP,
Willenborg C,
Gustafsson S,
Westra HJ,
Blades M,
de Craen AJ,
de Geus EJ,
Deelen J,
Grallert H,
Hamsten A,
Havulinna AS,
Hengstenberg C,
Houwing-Duistermaat JJ,
Hyppönen E,
Karssen LC,
Lehtimäki T,
Lyssenko V,
Magnusson PK,
Mihailov E,
Müller-Nurasyid M,
Mpindi JP,
Pedersen NL,
Penninx BW,
Perola M,
Pers TH,
Peters A,
Rung J,
Smit JH,
Steinthorsdottir V,
Tobin MD,
Tsernikova N,
van Leeuwen EM,
Viikari JS,
Willems SM,
Willemsen G,
Schunkert H,
Erdmann J,
Samani NJ,
Kaprio J,
Lind L,
Gieger C,
Metspalu A,
Slagboom PE,
Groop L,
van Duijn CM,
Eriksson JG,
Jula A,
Salomaa V,
Boomsma DI,
Power C,
Raitakari OT,
Ingelsson E,
Järvelin MR,
Thorsteinsdottir U,
Franke L,
Ikonen E,
Kallioniemi O,
Pietiäinen V,
Lindgren CM,
Stefansson K,
Palotie A,
McCarthy MI,
Morris AP,
Prokopenko I,
Ripatti S
ENGAGE Consortium
Nature genetics · 2015 · PMID 25961943
페이지 12개+
Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers
Lauc G,
Huffman JE,
Pučić M,
Zgaga L,
Adamczyk B,
Mužinić A,
Novokmet M,
Polašek O,
Gornik O,
Krištić J,
Keser T,
Vitart V
외 27명 — 모두 보기
Scheijen B,
Uh HW,
Molokhia M,
Patrick AL,
McKeigue P,
Kolčić I,
Lukić IK,
Swann O,
van Leeuwen FN,
Ruhaak LR,
Houwing-Duistermaat JJ,
Slagboom PE,
Beekman M,
de Craen AJ,
Deelder AM,
Zeng Q,
Wang W,
Hastie ND,
Gyllensten U,
Wilson JF,
Wuhrer M,
Wright AF,
Rudd PM,
Hayward C,
Aulchenko Y,
Campbell H,
Rudan I
PLoS genetics · 2013 · PMID 23382691 · open access
페이지 10개
A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function
Porcu E,
Medici M,
Pistis G,
Volpato CB,
Wilson SG,
Cappola AR,
Bos SD,
Deelen J,
den Heijer M,
Freathy RM,
Lahti J,
Liu C
외 82명 — 모두 보기
Lopez LM,
Nolte IM,
O'Connell JR,
Tanaka T,
Trompet S,
Arnold A,
Bandinelli S,
Beekman M,
Böhringer S,
Brown SJ,
Buckley BM,
Camaschella C,
de Craen AJ,
Davies G,
de Visser MC,
Ford I,
Forsen T,
Frayling TM,
Fugazzola L,
Gögele M,
Hattersley AT,
Hermus AR,
Hofman A,
Houwing-Duistermaat JJ,
Jensen RA,
Kajantie E,
Kloppenburg M,
Lim EM,
Masciullo C,
Mariotti S,
Minelli C,
Mitchell BD,
Nagaraja R,
Netea-Maier RT,
Palotie A,
Persani L,
Piras MG,
Psaty BM,
Räikkönen K,
Richards JB,
Rivadeneira F,
Sala C,
Sabra MM,
Sattar N,
Shields BM,
Soranzo N,
Starr JM,
Stott DJ,
Sweep FC,
Usala G,
van der Klauw MM,
van Heemst D,
van Mullem A,
Vermeulen SH,
Visser WE,
Walsh JP,
Westendorp RG,
Widen E,
Zhai G,
Cucca F,
Deary IJ,
Eriksson JG,
Ferrucci L,
Fox CS,
Jukema JW,
Kiemeney LA,
Pramstaller PP,
Schlessinger D,
Shuldiner AR,
Slagboom EP,
Uitterlinden AG,
Vaidya B,
Visser TJ,
Wolffenbuttel BH,
Meulenbelt I,
Rotter JI,
Spector TD,
Hicks AA,
Toniolo D,
Sanna S,
Peeters RP,
Naitza S
PLoS genetics · 2013 · PMID 23408906 · open access
페이지 10개
Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age
Deelen J,
Beekman M,
Uh HW,
Broer L,
Ayers KL,
Tan Q,
Kamatani Y,
Bennet AM,
Tamm R,
Trompet S,
Guðbjartsson DF,
Flachsbart F
외 75명 — 모두 보기
Rose G,
Viktorin A,
Fischer K,
Nygaard M,
Cordell HJ,
Crocco P,
van den Akker EB,
Böhringer S,
Helmer Q,
Nelson CP,
Saunders GI,
Alver M,
Andersen-Ranberg K,
Breen ME,
van der Breggen R,
Caliebe A,
Capri M,
Cevenini E,
Collerton JC,
Dato S,
Davies K,
Ford I,
Gampe J,
Garagnani P,
de Geus EJ,
Harrow J,
van Heemst D,
Heijmans BT,
Heinsen FA,
Hottenga JJ,
Hofman A,
Jeune B,
Jonsson PV,
Lathrop M,
Lechner D,
Martin-Ruiz C,
Mcnerlan SE,
Mihailov E,
Montesanto A,
Mooijaart SP,
Murphy A,
Nohr EA,
Paternoster L,
Postmus I,
Rivadeneira F,
Ross OA,
Salvioli S,
Sattar N,
Schreiber S,
Stefánsson H,
Stott DJ,
Tiemeier H,
Uitterlinden AG,
Westendorp RG,
Willemsen G,
Samani NJ,
Galan P,
Sørensen TI,
Boomsma DI,
Jukema JW,
Rea IM,
Passarino G,
de Craen AJ,
Christensen K,
Nebel A,
Stefánsson K,
Metspalu A,
Magnusson P,
Blanché H,
Christiansen L,
Kirkwood TB,
van Duijn CM,
Franceschi C,
Houwing-Duistermaat JJ,
Slagboom PE
Human molecular genetics · 2014 · PMID 24688116 · open access
페이지 2개
Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study
Zeggini E,
Panoutsopoulou K,
Southam L,
Rayner NW,
Day-Williams AG,
Lopes MC,
Boraska V,
Esko T,
Evangelou E,
Hoffman A,
Houwing-Duistermaat JJ,
Ingvarsson T
외 64명 — 모두 보기
Jonsdottir I,
Jonnson H,
Kerkhof HJ,
Kloppenburg M,
Bos SD,
Mangino M,
Metrustry S,
Slagboom PE,
Thorleifsson G,
Raine EV,
Ratnayake M,
Ricketts M,
Beazley C,
Blackburn H,
Bumpstead S,
Elliott KS,
Hunt SE,
Potter SC,
Shin SY,
Yadav VK,
Zhai G,
Sherburn K,
Dixon K,
Arden E,
Aslam N,
Battley PK,
Carluke I,
Doherty S,
Gordon A,
Joseph J,
Keen R,
Koller NC,
Mitchell S,
O'Neill F,
Paling E,
Reed MR,
Rivadeneira F,
Swift D,
Walker K,
Watkins B,
Wheeler M,
Birrell F,
Ioannidis JP,
Meulenbelt I,
Metspalu A,
Rai A,
Salter D,
Stefansson K,
Stykarsdottir U,
Uitterlinden AG,
van Meurs JB,
Chapman K,
Deloukas P,
Ollier WE,
Wallis GA,
Arden N,
Carr A,
Doherty M,
McCaskie A,
Willkinson JM,
Ralston SH,
Valdes AM,
Spector TD,
Loughlin J
arcOGEN Consortium · arcOGEN Collaborators
Lancet (London, England) · 2012 · PMID 22763110 · open access
페이지 1개
이 목록에 대한 질문
제 논문이 왜 여기 있습니까? 허락한 적이 없습니다.
논문의 내용은 여기에 전혀 옮겨져 있지 않습니다. 이 페이지가 기록하는 것은 MyGeneLog™의
어떤 페이지가 귀하의 연구를 인용하고 있다는 사실과 PubMed의 원문 링크뿐이며, 그것이 곧
인용입니다. 제목과 저자 목록은 도서관 목록이 쓰는 것과 같은 공개 기록인 Europe PMC에서
가져옵니다.
왜 "외 몇 명"이 아니라 저자를 다 적습니까?
622명이 필요했던 연구는 4명이 한 연구와 다른 종류의 연구인데, "et al."은 그것을 지우기
때문입니다. 12명을 먼저 보여 주고 나머지는 한 번 눌러 펼칩니다. 검색은 전원을 대상으로
합니다. 컨소시엄 논문의 187번째 이름도 실재하는 사람이고, 그 사람이 자기 이름을 찾고 있을
수 있습니다.
제 이름이 틀렸거나 논문 정보가 잘못되었습니다.
알려 주시면 고칩니다. 이름은 공개 기록에서 가져오는데 데이터베이스마다 이니셜 표기가
다르고, 같은 형태의 이름을 쓰는 두 사람을 저희가 구분할 수 없는 경우도 있습니다. 추측하기
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.