연구자에게
내 논문이 여기 있나요?
논문 2,657편이 이 사이트를 떠받치고 있습니다. 모든 변이·질환 페이지가
자기가 어떤 연구로부터 쓰였는지 밝히며, 이것이 그 목록을 페이지들에서 모은 것입니다.
성함이나 학술지명, PMID로 찾아보십시오.
Lanzani C에 대해
5건.
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
Winkler TW,
Justice AE,
Graff M,
Barata L,
Feitosa MF,
Chu S,
Czajkowski J,
Esko T,
Fall T,
Kilpeläinen TO,
Lu Y,
Mägi R
외 427명 — 모두 보기
Mihailov E,
Pers TH,
Rüeger S,
Teumer A,
Ehret GB,
Ferreira T,
Heard-Costa NL,
Karjalainen J,
Lagou V,
Mahajan A,
Neinast MD,
Prokopenko I,
Simino J,
Teslovich TM,
Jansen R,
Westra HJ,
White CC,
Absher D,
Ahluwalia TS,
Ahmad S,
Albrecht E,
Alves AC,
Bragg-Gresham JL,
de Craen AJ,
Bis JC,
Bonnefond A,
Boucher G,
Cadby G,
Cheng YC,
Chiang CW,
Delgado G,
Demirkan A,
Dueker N,
Eklund N,
Eiriksdottir G,
Eriksson J,
Feenstra B,
Fischer K,
Frau F,
Galesloot TE,
Geller F,
Goel A,
Gorski M,
Grammer TB,
Gustafsson S,
Haitjema S,
Hottenga JJ,
Huffman JE,
Jackson AU,
Jacobs KB,
Johansson Å,
Kaakinen M,
Kleber ME,
Lahti J,
Mateo Leach I,
Lehne B,
Liu Y,
Lo KS,
Lorentzon M,
Luan J,
Madden PA,
Mangino M,
McKnight B,
Medina-Gomez C,
Monda KL,
Montasser ME,
Müller G,
Müller-Nurasyid M,
Nolte IM,
Panoutsopoulou K,
Pascoe L,
Paternoster L,
Rayner NW,
Renström F,
Rizzi F,
Rose LM,
Ryan KA,
Salo P,
Sanna S,
Scharnagl H,
Shi J,
Smith AV,
Southam L,
Stančáková A,
Steinthorsdottir V,
Strawbridge RJ,
Sung YJ,
Tachmazidou I,
Tanaka T,
Thorleifsson G,
Trompet S,
Pervjakova N,
Tyrer JP,
Vandenput L,
van der Laan SW,
van der Velde N,
van Setten J,
van Vliet-Ostaptchouk JV,
Verweij N,
Vlachopoulou E,
Waite LL,
Wang SR,
Wang Z,
Wild SH,
Willenborg C,
Wilson JF,
Wong A,
Yang J,
Yengo L,
Yerges-Armstrong LM,
Yu L,
Zhang W,
Zhao JH,
Andersson EA,
Bakker SJ,
Baldassarre D,
Banasik K,
Barcella M,
Barlassina C,
Bellis C,
Benaglio P,
Blangero J,
Blüher M,
Bonnet F,
Bonnycastle LL,
Boyd HA,
Bruinenberg M,
Buchman AS,
Campbell H,
Chen YD,
Chines PS,
Claudi-Boehm S,
Cole J,
Collins FS,
de Geus EJ,
de Groot LC,
Dimitriou M,
Duan J,
Enroth S,
Eury E,
Farmaki AE,
Forouhi NG,
Friedrich N,
Gejman PV,
Gigante B,
Glorioso N,
Go AS,
Gottesman O,
Gräßler J,
Grallert H,
Grarup N,
Gu YM,
Broer L,
Ham AC,
Hansen T,
Harris TB,
Hartman CA,
Hassinen M,
Hastie N,
Hattersley AT,
Heath AC,
Henders AK,
Hernandez D,
Hillege H,
Holmen O,
Hovingh KG,
Hui J,
Husemoen LL,
Hutri-Kähönen N,
Hysi PG,
Illig T,
De Jager PL,
Jalilzadeh S,
Jørgensen T,
Jukema JW,
Juonala M,
Kanoni S,
Karaleftheri M,
Khaw KT,
Kinnunen L,
Kittner SJ,
Koenig W,
Kolcic I,
Kovacs P,
Krarup NT,
Kratzer W,
Krüger J,
Kuh D,
Kumari M,
Kyriakou T,
Langenberg C,
Lannfelt L,
Lanzani C,
Lotay V,
Launer LJ,
Leander K,
Lindström J,
Linneberg A,
Liu YP,
Lobbens S,
Luben R,
Lyssenko V,
Männistö S,
Magnusson PK,
McArdle WL,
Menni C,
Merger S,
Milani L,
Montgomery GW,
Morris AP,
Narisu N,
Nelis M,
Ong KK,
Palotie A,
Pérusse L,
Pichler I,
Pilia MG,
Pouta A,
Rheinberger M,
Ribel-Madsen R,
Richards M,
Rice KM,
Rice TK,
Rivolta C,
Salomaa V,
Sanders AR,
Sarzynski MA,
Scholtens S,
Scott RA,
Scott WR,
Sebert S,
Sengupta S,
Sennblad B,
Seufferlein T,
Silveira A,
Slagboom PE,
Smit JH,
Sparsø TH,
Stirrups K,
Stolk RP,
Stringham HM,
Swertz MA,
Swift AJ,
Syvänen AC,
Tan ST,
Thorand B,
Tönjes A,
Tremblay A,
Tsafantakis E,
van der Most PJ,
Völker U,
Vohl MC,
Vonk JM,
Waldenberger M,
Walker RW,
Wennauer R,
Widén E,
Willemsen G,
Wilsgaard T,
Wright AF,
Zillikens MC,
van Dijk SC,
van Schoor NM,
Asselbergs FW,
de Bakker PI,
Beckmann JS,
Beilby J,
Bennett DA,
Bergman RN,
Bergmann S,
Böger CA,
Boehm BO,
Boerwinkle E,
Boomsma DI,
Bornstein SR,
Bottinger EP,
Bouchard C,
Chambers JC,
Chanock SJ,
Chasman DI,
Cucca F,
Cusi D,
Dedoussis G,
Erdmann J,
Eriksson JG,
Evans DA,
de Faire U,
Farrall M,
Ferrucci L,
Ford I,
Franke L,
Franks PW,
Froguel P,
Gansevoort RT,
Gieger C,
Grönberg H,
Gudnason V,
Gyllensten U,
Hall P,
Hamsten A,
van der Harst P,
Hayward C,
Heliövaara M,
Hengstenberg C,
Hicks AA,
Hingorani A,
Hofman A,
Hu F,
Huikuri HV,
Hveem K,
James AL,
Jordan JM,
Jula A,
Kähönen M,
Kajantie E,
Kathiresan S,
Kiemeney LA,
Kivimaki M,
Knekt PB,
Koistinen HA,
Kooner JS,
Koskinen S,
Kuusisto J,
Maerz W,
Martin NG,
Laakso M,
Lakka TA,
Lehtimäki T,
Lettre G,
Levinson DF,
Lind L,
Lokki ML,
Mäntyselkä P,
Melbye M,
Metspalu A,
Mitchell BD,
Moll FL,
Murray JC,
Musk AW,
Nieminen MS,
Njølstad I,
Ohlsson C,
Oldehinkel AJ,
Oostra BA,
Palmer LJ,
Pankow JS,
Pasterkamp G,
Pedersen NL,
Pedersen O,
Penninx BW,
Perola M,
Peters A,
Polašek O,
Pramstaller PP,
Psaty BM,
Qi L,
Quertermous T,
Raitakari OT,
Rankinen T,
Rauramaa R,
Ridker PM,
Rioux JD,
Rivadeneira F,
Rotter JI,
Rudan I,
den Ruijter HM,
Saltevo J,
Sattar N,
Schunkert H,
Schwarz PE,
Shuldiner AR,
Sinisalo J,
Snieder H,
Sørensen TI,
Spector TD,
Staessen JA,
Stefania B,
Thorsteinsdottir U,
Stumvoll M,
Tardif JC,
Tremoli E,
Tuomilehto J,
Uitterlinden AG,
Uusitupa M,
Verbeek AL,
Vermeulen SH,
Viikari JS,
Vitart V,
Völzke H,
Vollenweider P,
Waeber G,
Walker M,
Wallaschofski H,
Wareham NJ,
Watkins H,
Zeggini E,
Chakravarti A,
Clegg DJ,
Cupples LA,
Gordon-Larsen P,
Jaquish CE,
Rao DC,
Abecasis GR,
Assimes TL,
Barroso I,
Berndt SI,
Boehnke M,
Deloukas P,
Fox CS,
Groop LC,
Hunter DJ,
Ingelsson E,
Kaplan RC,
McCarthy MI,
Mohlke KL,
O'Connell JR,
Schlessinger D,
Strachan DP,
Stefansson K,
van Duijn CM,
Hirschhorn JN,
Lindgren CM,
Heid IM,
North KE,
Borecki IB,
Kutalik Z,
Loos RJ
CHARGE Consortium · DIAGRAM Consortium 외 컨소시엄 4곳
PLoS genetics · 2015 · PMID 26426971 · open access
페이지 12개+
Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy
Tadros R,
Zheng SL,
Grace C,
Jordà P,
Francis C,
West DM,
Jurgens SJ,
Thomson KL,
Harper AR,
Ormondroyd E,
Xu X,
Theotokis PI
외 50명 — 모두 보기
Buchan RJ,
McGurk KA,
Mazzarotto F,
Boschi B,
Pelo E,
Lee M,
Noseda M,
Varnava A,
Vermeer AMC,
Walsh R,
Amin AS,
van Slegtenhorst MA,
Roslin NM,
Strug LJ,
Salvi E,
Lanzani C,
de Marvao A,
Roberts JD,
Tremblay-Gravel M,
Giraldeau G,
Cadrin-Tourigny J,
L'Allier PL,
Garceau P,
Talajic M,
Gagliano Taliun SA,
Pinto YM,
Rakowski H,
Pantazis A,
Bai W,
Baksi J,
Halliday BP,
Prasad SK,
Barton PJR,
O'Regan DP,
Cook SA,
de Boer RA,
Christiaans I,
Michels M,
Kramer CM,
Ho CY,
Neubauer S,
Matthews PM,
Wilde AAM,
Tardif JC,
Olivotto I,
Adler A,
Goel A,
Ware JS,
Bezzina CR,
Watkins H
Hypergenes InterOmics Collaborators · HCMR Investigators
Nature genetics · 2025 · PMID 39966646 · open access
페이지 12개+
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Speliotes EK,
Willer CJ,
Berndt SI,
Monda KL,
Thorleifsson G,
Jackson AU,
Lango Allen H,
Lindgren CM,
Luan J,
Mägi R,
Randall JC,
Vedantam S
외 366명 — 모두 보기
Winkler TW,
Qi L,
Workalemahu T,
Heid IM,
Steinthorsdottir V,
Stringham HM,
Weedon MN,
Wheeler E,
Wood AR,
Ferreira T,
Weyant RJ,
Segrè AV,
Estrada K,
Liang L,
Nemesh J,
Park JH,
Gustafsson S,
Kilpeläinen TO,
Yang J,
Bouatia-Naji N,
Esko T,
Feitosa MF,
Kutalik Z,
Mangino M,
Raychaudhuri S,
Scherag A,
Smith AV,
Welch R,
Zhao JH,
Aben KK,
Absher DM,
Amin N,
Dixon AL,
Fisher E,
Glazer NL,
Goddard ME,
Heard-Costa NL,
Hoesel V,
Hottenga JJ,
Johansson A,
Johnson T,
Ketkar S,
Lamina C,
Li S,
Moffatt MF,
Myers RH,
Narisu N,
Perry JR,
Peters MJ,
Preuss M,
Ripatti S,
Rivadeneira F,
Sandholt C,
Scott LJ,
Timpson NJ,
Tyrer JP,
van Wingerden S,
Watanabe RM,
White CC,
Wiklund F,
Barlassina C,
Chasman DI,
Cooper MN,
Jansson JO,
Lawrence RW,
Pellikka N,
Prokopenko I,
Shi J,
Thiering E,
Alavere H,
Alibrandi MT,
Almgren P,
Arnold AM,
Aspelund T,
Atwood LD,
Balkau B,
Balmforth AJ,
Bennett AJ,
Ben-Shlomo Y,
Bergman RN,
Bergmann S,
Biebermann H,
Blakemore AI,
Boes T,
Bonnycastle LL,
Bornstein SR,
Brown MJ,
Buchanan TA,
Busonero F,
Campbell H,
Cappuccio FP,
Cavalcanti-Proença C,
Chen YD,
Chen CM,
Chines PS,
Clarke R,
Coin L,
Connell J,
Day IN,
den Heijer M,
Duan J,
Ebrahim S,
Elliott P,
Elliott P,
Elosua R,
Eiriksdottir G,
Erdos MR,
Eriksson JG,
Facheris MF,
Felix SB,
Fischer-Posovszky P,
Folsom AR,
Friedrich N,
Freimer NB,
Fu M,
Gaget S,
Gejman PV,
Geus EJ,
Gieger C,
Gjesing AP,
Goel A,
Goyette P,
Grallert H,
Grässler J,
Greenawalt DM,
Groves CJ,
Gudnason V,
Guiducci C,
Hartikainen AL,
Hassanali N,
Hall AS,
Havulinna AS,
Hayward C,
Heath AC,
Hengstenberg C,
Hicks AA,
Hinney A,
Hofman A,
Homuth G,
Hui J,
Igl W,
Iribarren C,
Isomaa B,
Jacobs KB,
Jarick I,
Jewell E,
John U,
Jørgensen T,
Jousilahti P,
Jula A,
Kaakinen M,
Kajantie E,
Kaplan LM,
Kathiresan S,
Kettunen J,
Kinnunen L,
Knowles JW,
Kolcic I,
König IR,
Koskinen S,
Kovacs P,
Kuusisto J,
Kraft P,
Kvaløy K,
Laitinen J,
Lantieri O,
Lanzani C,
Launer LJ,
Lecoeur C,
Lehtimäki T,
Lettre G,
Liu J,
Lokki ML,
Lorentzon M,
Luben RN,
Ludwig B,
Manunta P,
Marek D,
Marre M,
Martin NG,
McArdle WL,
McCarthy A,
McKnight B,
Meitinger T,
Melander O,
Meyre D,
Midthjell K,
Montgomery GW,
Morken MA,
Morris AP,
Mulic R,
Ngwa JS,
Nelis M,
Neville MJ,
Nyholt DR,
O'Donnell CJ,
O'Rahilly S,
Ong KK,
Oostra B,
Paré G,
Parker AN,
Perola M,
Pichler I,
Pietiläinen KH,
Platou CG,
Polasek O,
Pouta A,
Rafelt S,
Raitakari O,
Rayner NW,
Ridderstråle M,
Rief W,
Ruokonen A,
Robertson NR,
Rzehak P,
Salomaa V,
Sanders AR,
Sandhu MS,
Sanna S,
Saramies J,
Savolainen MJ,
Scherag S,
Schipf S,
Schreiber S,
Schunkert H,
Silander K,
Sinisalo J,
Siscovick DS,
Smit JH,
Soranzo N,
Sovio U,
Stephens J,
Surakka I,
Swift AJ,
Tammesoo ML,
Tardif JC,
Teder-Laving M,
Teslovich TM,
Thompson JR,
Thomson B,
Tönjes A,
Tuomi T,
van Meurs JB,
van Ommen GJ,
Vatin V,
Viikari J,
Visvikis-Siest S,
Vitart V,
Vogel CI,
Voight BF,
Waite LL,
Wallaschofski H,
Walters GB,
Widen E,
Wiegand S,
Wild SH,
Willemsen G,
Witte DR,
Witteman JC,
Xu J,
Zhang Q,
Zgaga L,
Ziegler A,
Zitting P,
Beilby JP,
Farooqi IS,
Hebebrand J,
Huikuri HV,
James AL,
James AL,
Kähönen M,
Levinson DF,
Macciardi F,
Nieminen MS,
Ohlsson C,
Palmer LJ,
Ridker PM,
Stumvoll M,
Beckmann JS,
Boeing H,
Boerwinkle E,
Boomsma DI,
Caulfield MJ,
Chanock SJ,
Collins FS,
Cupples LA,
Smith GD,
Erdmann J,
Froguel P,
Grönberg H,
Gyllensten U,
Hall P,
Hansen T,
Harris TB,
Hattersley AT,
Hayes RB,
Heinrich J,
Hu FB,
Hveem K,
Illig T,
Jarvelin MR,
Kaprio J,
Karpe F,
Khaw KT,
Kiemeney LA,
Krude H,
Laakso M,
Lawlor DA,
Metspalu A,
Munroe PB,
Ouwehand WH,
Pedersen O,
Penninx BW,
Peters A,
Pramstaller PP,
Quertermous T,
Reinehr T,
Rissanen A,
Rudan I,
Samani NJ,
Schwarz PE,
Schwarz PE,
Shuldiner AR,
Spector TD,
Tuomilehto J,
Uda M,
Uitterlinden A,
Valle TT,
Wabitsch M,
Waeber G,
Wareham NJ,
Watkins H,
Wilson JF,
Wright AF,
Zillikens MC,
Chatterjee N,
McCarroll SA,
Purcell S,
Schadt EE,
Visscher PM,
Assimes TL,
Borecki IB,
Deloukas P,
Fox CS,
Groop LC,
Haritunians T,
Hunter DJ,
Kaplan RC,
Mohlke KL,
O'Connell JR,
Peltonen L,
Schlessinger D,
Strachan DP,
van Duijn CM,
Wichmann HE,
Frayling TM,
Thorsteinsdottir U,
Abecasis GR,
Barroso I,
Boehnke M,
Stefansson K,
North KE,
McCarthy MI,
Hirschhorn JN,
Ingelsson E,
Loos RJ
MAGIC · Procardis Consortium
Nature genetics · 2010 · PMID 20935630 · open access
페이지 11개
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
Genome-Wide Meta-Analysis Identifies Three Novel Susceptibility Loci and Reveals Ethnic Heterogeneity of Genetic Susceptibility for IgA Nephropathy
Li M,
Wang L,
Shi DC,
Foo JN,
Zhong Z,
Khor CC,
Lanzani C,
Citterio L,
Salvi E,
Yin PR,
Bei JX,
Wang L
외 13명 — 모두 보기
Liao YH,
Chen J,
Chen QK,
Xu G,
Jiang GR,
Wan JX,
Chen MH,
Chen N,
Zhang H,
Zeng YX,
Liu ZH,
Liu JJ,
Yu XQ
Journal of the American Society of Nephrology : JASN · 2020 · PMID 32912934
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.