연구자에게
내 논문이 여기 있나요?
논문 2,675편이 이 사이트를 떠받치고 있습니다. 모든 변이·질환 페이지가
자기가 어떤 연구로부터 쓰였는지 밝히며, 이것이 그 목록을 페이지들에서 모은 것입니다.
성함이나 학술지명, PMID로 찾아보십시오.
Jorgenson E에 대해
35건, 그중 15건 표시.
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology
Ferreira MA,
Vonk JM,
Baurecht H,
Marenholz I,
Tian C,
Hoffman JD,
Helmer Q,
Tillander A,
Ullemar V,
van Dongen J,
Lu Y,
Rüschendorf F
외 54명 — 모두 보기
Esparza-Gordillo J,
Medway CW,
Mountjoy E,
Burrows K,
Hummel O,
Grosche S,
Brumpton BM,
Witte JS,
Hottenga JJ,
Willemsen G,
Zheng J,
Rodríguez E,
Hotze M,
Franke A,
Revez JA,
Beesley J,
Matheson MC,
Dharmage SC,
Bain LM,
Fritsche LG,
Gabrielsen ME,
Balliu B,
Nielsen JB,
Zhou W,
Hveem K,
Langhammer A,
Holmen OL,
Løset M,
Abecasis GR,
Willer CJ,
Arnold A,
Homuth G,
Schmidt CO,
Thompson PJ,
Martin NG,
Duffy DL,
Novak N,
Schulz H,
Karrasch S,
Gieger C,
Strauch K,
Melles RB,
Hinds DA,
Hübner N,
Weidinger S,
Magnusson PKE,
Jansen R,
Jorgenson E,
Lee YA,
Boomsma DI,
Almqvist C,
Karlsson R,
Koppelman GH,
Paternoster L
23andMe Research Team · AAGC collaborators 외 컨소시엄 2곳
Nature genetics · 2017 · PMID 29083406 · open access
페이지 10개
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
Wray NR,
Ripke S,
Mattheisen M,
Trzaskowski M,
Byrne EM,
Abdellaoui A,
Adams MJ,
Agerbo E,
Air TM,
Andlauer TMF,
Bacanu SA,
Bækvad-Hansen M
외 205명 — 모두 보기
Beekman AFT,
Bigdeli TB,
Binder EB,
Blackwood DRH,
Bryois J,
Buttenschøn HN,
Bybjerg-Grauholm J,
Cai N,
Castelao E,
Christensen JH,
Clarke TK,
Coleman JIR,
Colodro-Conde L,
Couvy-Duchesne B,
Craddock N,
Crawford GE,
Crowley CA,
Dashti HS,
Davies G,
Deary IJ,
Degenhardt F,
Derks EM,
Direk N,
Dolan CV,
Dunn EC,
Eley TC,
Eriksson N,
Escott-Price V,
Kiadeh FHF,
Finucane HK,
Forstner AJ,
Frank J,
Gaspar HA,
Gill M,
Giusti-Rodríguez P,
Goes FS,
Gordon SD,
Grove J,
Hall LS,
Hannon E,
Hansen CS,
Hansen TF,
Herms S,
Hickie IB,
Hoffmann P,
Homuth G,
Horn C,
Hottenga JJ,
Hougaard DM,
Hu M,
Hyde CL,
Ising M,
Jansen R,
Jansen R,
Jin F,
Jorgenson E,
Knowles JA,
Kohane IS,
Kraft J,
Kretzschmar WW,
Krogh J,
Kutalik Z,
Lane JM,
Li Y,
Li Y,
Lind PA,
Liu X,
Lu L,
MacIntyre DJ,
MacKinnon DF,
Maier RM,
Maier W,
Marchini J,
Mbarek H,
McGrath P,
McGuffin P,
Medland SE,
Mehta D,
Middeldorp CM,
Mihailov E,
Milaneschi Y,
Milani L,
Mill J,
Mondimore FM,
Montgomery GW,
Mostafavi S,
Mullins N,
Nauck M,
Ng B,
Nivard MG,
Nyholt DR,
O'Reilly PF,
Oskarsson H,
Owen MJ,
Painter JN,
Pedersen CB,
Pedersen MG,
Peterson RE,
Pettersson E,
Peyrot WJ,
Pistis G,
Posthuma D,
Purcell SM,
Quiroz JA,
Qvist P,
Rice JP,
Riley BP,
Rivera M,
Saeed Mirza S,
Saxena R,
Schoevers R,
Schulte EC,
Shen L,
Shi J,
Shyn SI,
Sigurdsson E,
Sinnamon GBC,
Smit JH,
Smith DJ,
Stefansson H,
Steinberg S,
Stockmeier CA,
Streit F,
Strohmaier J,
Tansey KE,
Teismann H,
Teumer A,
Thompson W,
Thomson PA,
Thorgeirsson TE,
Tian C,
Traylor M,
Treutlein J,
Trubetskoy V,
Uitterlinden AG,
Umbricht D,
Van der Auwera S,
van Hemert AM,
Viktorin A,
Visscher PM,
Wang Y,
Webb BT,
Weinsheimer SM,
Wellmann J,
Willemsen G,
Witt SH,
Wu Y,
Xi HS,
Yang J,
Zhang F,
Arolt V,
Baune BT,
Berger K,
Boomsma DI,
Cichon S,
Dannlowski U,
de Geus ECJ,
DePaulo JR,
Domenici E,
Domschke K,
Esko T,
Grabe HJ,
Hamilton SP,
Hayward C,
Heath AC,
Hinds DA,
Kendler KS,
Kloiber S,
Lewis G,
Li QS,
Lucae S,
Madden PFA,
Magnusson PK,
Martin NG,
McIntosh AM,
Metspalu A,
Mors O,
Mortensen PB,
Müller-Myhsok B,
Nordentoft M,
Nöthen MM,
O'Donovan MC,
Paciga SA,
Pedersen NL,
Penninx BWJH,
Perlis RH,
Porteous DJ,
Potash JB,
Preisig M,
Rietschel M,
Schaefer C,
Schulze TG,
Smoller JW,
Stefansson K,
Tiemeier H,
Uher R,
Völzke H,
Weissman MM,
Werge T,
Winslow AR,
Lewis CM,
Levinson DF,
Breen G,
Børglum AD,
Sullivan PF
eQTLGen · 23andMe 외 컨소시엄 1곳
Nature genetics · 2018 · PMID 29700475 · open access
페이지 10개
Age-of-onset information helps identify 76 genetic variants associated with allergic disease
Ferreira MAR,
Vonk JM,
Baurecht H,
Marenholz I,
Tian C,
Hoffman JD,
Helmer Q,
Tillander A,
Ullemar V,
Lu Y,
Grosche S,
Rüschendorf F
외 28명 — 모두 보기
Granell R,
Brumpton BM,
Fritsche LG,
Bhatta L,
Gabrielsen ME,
Nielsen JB,
Zhou W,
Hveem K,
Langhammer A,
Holmen OL,
Løset M,
Abecasis GR,
Willer CJ,
Emami NC,
Cavazos TB,
Witte JS,
Szwajda A,
Hinds DA,
Hübner N,
Weidinger S,
Magnusson PK,
Jorgenson E,
Karlsson R,
Paternoster L,
Boomsma DI,
Almqvist C,
Lee YA,
Koppelman GH
23andMe Research Team · collaborators of the SHARE study
PLoS genetics · 2020 · PMID 32603359 · open access
페이지 7개
Genome-wide association study of prostate-specific antigen levels identifies novel loci independent of prostate cancer
Hoffmann TJ,
Passarelli MN,
Graff RE,
Emami NC,
Sakoda LC,
Jorgenson E,
Habel LA,
Shan J,
Ranatunga DK,
Quesenberry CP,
Chao CR,
Ghai NR
외 17명 — 모두 보기
Aaronson D,
Presti J,
Nordström T,
Wang Z,
Berndt SI,
Chanock SJ,
Mosley JD,
Klein RJ,
Middha M,
Lilja H,
Melander O,
Kvale MN,
Kwok PY,
Schaefer C,
Risch N,
Van Den Eeden SK,
Witte JS
Nature communications · 2017 · PMID 28139693 · open access
페이지 5개
A large multiethnic genome-wide association study of prostate cancer identifies novel risk variants and substantial ethnic differences
Hoffmann TJ,
Van Den Eeden SK,
Sakoda LC,
Jorgenson E,
Habel LA,
Graff RE,
Passarelli MN,
Cario CL,
Emami NC,
Chao CR,
Ghai NR,
Shan J
외 23명 — 모두 보기
Ranatunga DK,
Quesenberry CP,
Aaronson D,
Presti J,
Wang Z,
Berndt SI,
Chanock SJ,
McDonnell SK,
French AJ,
Schaid DJ,
Thibodeau SN,
Li Q,
Freedman ML,
Penney KL,
Mucci LA,
Haiman CA,
Henderson BE,
Seminara D,
Kvale MN,
Kwok PY,
Schaefer C,
Risch N,
Witte JS
Cancer discovery · 2015 · PMID 26034056
페이지 3개
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
Kowalski MH,
Qian H,
Hou Z,
Rosen JD,
Tapia AL,
Shan Y,
Jain D,
Argos M,
Arnett DK,
Avery C,
Barnes KC,
Becker LC
외 66명 — 모두 보기
Bien SA,
Bis JC,
Blangero J,
Boerwinkle E,
Bowden DW,
Buyske S,
Cai J,
Cho MH,
Choi SH,
Choquet H,
Cupples LA,
Cushman M,
Daya M,
de Vries PS,
Ellinor PT,
Faraday N,
Fornage M,
Gabriel S,
Ganesh SK,
Graff M,
Gupta N,
He J,
Heckbert SR,
Hidalgo B,
Hodonsky CJ,
Irvin MR,
Johnson AD,
Jorgenson E,
Kaplan R,
Kardia SLR,
Kelly TN,
Kooperberg C,
Lasky-Su JA,
Loos RJF,
Lubitz SA,
Mathias RA,
McHugh CP,
Montgomery C,
Moon JY,
Morrison AC,
Palmer ND,
Pankratz N,
Papanicolaou GJ,
Peralta JM,
Peyser PA,
Rich SS,
Rotter JI,
Silverman EK,
Smith JA,
Smith NL,
Taylor KD,
Thornton TA,
Tiwari HK,
Tracy RP,
Wang T,
Weiss ST,
Weng LC,
Wiggins KL,
Wilson JG,
Yanek LR,
Zöllner S,
North KE,
Auer PL,
Raffield LM,
Reiner AP,
Li Y
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium · TOPMed Hematology & Hemostasis Working Group
PLoS genetics · 2019 · PMID 31869403 · open access
페이지 3개
Identification of 31 loci for mammographic density phenotypes and their associations with breast cancer risk
Sieh W,
Rothstein JH,
Klein RJ,
Alexeeff SE,
Sakoda LC,
Jorgenson E,
McBride RB,
Graff RE,
McGuire V,
Achacoso N,
Acton L,
Liang RY
외 8명 — 모두 보기
Nature communications · 2020 · PMID 33037222 · open access
페이지 3개
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative
Little A,
Hu Y,
Sun Q,
Jain D,
Broome J,
Chen MH,
Thibord F,
McHugh C,
Surendran P,
Blackwell TW,
Brody JA,
Bhan A
외 55명 — 모두 보기
Chami N,
de Vries PS,
Ekunwe L,
Heard-Costa N,
Hobbs BD,
Manichaikul A,
Moon JY,
Preuss MH,
Ryan K,
Wang Z,
Wheeler M,
Yanek LR,
Abecasis GR,
Almasy L,
Beaty TH,
Becker LC,
Blangero J,
Boerwinkle E,
Butterworth AS,
Choquet H,
Correa A,
Curran JE,
Faraday N,
Fornage M,
Glahn DC,
Hou L,
Jorgenson E,
Kooperberg C,
Lewis JP,
Lloyd-Jones DM,
Loos RJF,
Min YI,
Mitchell BD,
Morrison AC,
Nickerson DA,
North KE,
O'Connell JR,
Pankratz N,
Psaty BM,
Vasan RS,
Rich SS,
Rotter JI,
Smith AV,
Smith NL,
Tang H,
Tracy RP,
Conomos MP,
Laurie CA,
Mathias RA,
Li Y,
Auer PL,
Thornton T,
Reiner AP,
Johnson AD,
Raffield LM
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Human molecular genetics · 2022 · PMID 34553764
페이지 2개
A multiethnic genome-wide analysis of 19,420 individuals identifies novel loci associated with axial length and shared genetic influences with refractive error and myopia
Jiang C,
Melles RB,
Yin J,
Fan Q,
Guo X,
Cheng CY,
He M,
Mackey DA,
Guggenheim JA,
Klaver C,
Nair KS,
Jorgenson E
외 1명 — 모두 보기
Consortium for Refractive Error and Myopia (CREAM)
Frontiers in genetics · 2023 · PMID 37351342 · open access
페이지 2개
Genome-wide meta-analyses of smoking behaviors in African Americans
David SP,
Hamidovic A,
Chen GK,
Bergen AW,
Wessel J,
Kasberger JL,
Brown WM,
Petruzella S,
Thacker EL,
Kim Y,
Nalls MA,
Tranah GJ
외 68명 — 모두 보기
Sung YJ,
Ambrosone CB,
Arnett D,
Bandera EV,
Becker DM,
Becker L,
Berndt SI,
Bernstein L,
Blot WJ,
Broeckel U,
Buxbaum SG,
Caporaso N,
Casey G,
Chanock SJ,
Deming SL,
Diver WR,
Eaton CB,
Evans DS,
Evans MK,
Fornage M,
Franceschini N,
Harris TB,
Henderson BE,
Hernandez DG,
Hitsman B,
Hu JJ,
Hunt SC,
Ingles SA,
John EM,
Kittles R,
Kolb S,
Kolonel LN,
Le Marchand L,
Liu Y,
Lohman KK,
McKnight B,
Millikan RC,
Murphy A,
Neslund-Dudas C,
Nyante S,
Press M,
Psaty BM,
Rao DC,
Redline S,
Rodriguez-Gil JL,
Rybicki BA,
Signorello LB,
Singleton AB,
Smoller J,
Snively B,
Spring B,
Stanford JL,
Strom SS,
Swan GE,
Taylor KD,
Thun MJ,
Wilson AF,
Witte JS,
Yamamura Y,
Yanek LR,
Yu K,
Zheng W,
Zheng W,
Ziegler RG,
Zonderman AB,
Jorgenson E,
Haiman CA,
Furberg H
Translational psychiatry · 2012 · PMID 22832964 · open access
페이지 1개
Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry
Hauser MA,
Allingham RR,
Aung T,
Van Der Heide CJ,
Taylor KD,
Rotter JI,
Wang SJ,
Bonnemaijer PWM,
Williams SE,
Abdullahi SM,
Abu-Amero KK,
Anderson MG
외 81명 — 모두 보기
Akafo S,
Alhassan MB,
Asimadu I,
Ayyagari R,
Bakayoko S,
Nyamsi PB,
Bowden DW,
Bromley WC,
Budenz DL,
Carmichael TR,
Challa P,
Chen YI,
Chuka-Okosa CM,
Cooke Bailey JN,
Costa VP,
Cruz DA,
DuBiner H,
Ervin JF,
Feldman RM,
Flamme-Wiese M,
Gaasterland DE,
Garnai SJ,
Girkin CA,
Guirou N,
Guo X,
Haines JL,
Hammond CJ,
Herndon L,
Hoffmann TJ,
Hulette CM,
Hydara A,
Igo RP Jr,
Jorgenson E,
Kabwe J,
Kilangalanga NJ,
Kizor-Akaraiwe N,
Kuchtey RW,
Lamari H,
Li Z,
Liebmann JM,
Liu Y,
Loos RJF,
Melo MB,
Moroi SE,
Msosa JM,
Mullins RF,
Nadkarni G,
Napo A,
Ng MCY,
Nunes HF,
Obeng-Nyarkoh E,
Okeke A,
Okeke S,
Olaniyi O,
Olawoye O,
Oliveira MB,
Pasquale LR,
Perez-Grossmann RA,
Pericak-Vance MA,
Qin X,
Ramsay M,
Resnikoff S,
Richards JE,
Schimiti RB,
Sim KS,
Sponsel WE,
Svidnicki PV,
Thiadens AAHJ,
Uche NJ,
van Duijn CM,
de Vasconcellos JPC,
Wiggs JL,
Zangwill LM,
Risch N,
Milea D,
Ashaye A,
Klaver CCW,
Weinreb RN,
Ashley Koch AE,
Fingert JH,
Khor CC
Genetics of Glaucoma in People of African Descent (GGLAD) Consortium
JAMA · 2019 · PMID 31688885
페이지 1개
A Large-Scale Association Study Detects Novel Rare Variants, Risk Genes, Functional Elements, and Polygenic Architecture of Prostate Cancer Susceptibility
Emami NC,
Cavazos TB,
Rashkin SR,
Cario CL,
Graff RE,
Tai CG,
Mefford JA,
Kachuri L,
Wan E,
Wong S,
Aaronson D,
Presti J
외 14명 — 모두 보기
Habel LA,
Shan J,
Ranatunga DK,
Chao CR,
Ghai NR,
Jorgenson E,
Sakoda LC,
Kvale MN,
Kwok PY,
Schaefer C,
Risch N,
Hoffmann TJ,
Van Den Eeden SK,
Witte JS
Cancer research · 2021 · PMID 33293427
페이지 1개
Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program
Mikhaylova AV,
McHugh CP,
Polfus LM,
Raffield LM,
Boorgula MP,
Blackwell TW,
Brody JA,
Broome J,
Chami N,
Chen MH,
Conomos MP,
Cox C
외 81명 — 모두 보기
Curran JE,
Daya M,
Ekunwe L,
Glahn DC,
Heard-Costa N,
Highland HM,
Hobbs BD,
Ilboudo Y,
Jain D,
Lange LA,
Miller-Fleming TW,
Min N,
Moon JY,
Preuss MH,
Rosen J,
Ryan K,
Smith AV,
Sun Q,
Surendran P,
de Vries PS,
Walter K,
Wang Z,
Wheeler M,
Yanek LR,
Zhong X,
Abecasis GR,
Almasy L,
Barnes KC,
Beaty TH,
Becker LC,
Blangero J,
Boerwinkle E,
Butterworth AS,
Chavan S,
Cho MH,
Choquet H,
Correa A,
Cox N,
DeMeo DL,
Faraday N,
Fornage M,
Gerszten RE,
Hou L,
Johnson AD,
Jorgenson E,
Kaplan R,
Kooperberg C,
Kundu K,
Laurie CA,
Lettre G,
Lewis JP,
Li B,
Li Y,
Lloyd-Jones DM,
Loos RJF,
Manichaikul A,
Meyers DA,
Mitchell BD,
Morrison AC,
Ngo D,
Nickerson DA,
Nongmaithem S,
North KE,
O'Connell JR,
Ortega VE,
Pankratz N,
Perry JA,
Psaty BM,
Rich SS,
Soranzo N,
Rotter JI,
Silverman EK,
Smith NL,
Tang H,
Tracy RP,
Thornton TA,
Vasan RS,
Zein J,
Mathias RA,
Reiner AP,
Auer PL
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
American journal of human genetics · 2021 · PMID 34582791
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.