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661 matches for
Er J,
showing the first 20.
Association analyses based on false discovery rate implicate new loci for coronary artery disease
Nelson CP,
Goel A,
Butterworth AS,
Kanoni S,
Webb TR,
Marouli E,
Zeng L,
Ntalla I,
Lai FY,
Hopewell JC,
Giannakopoulou O,
Jiang T
and 50 more — show all
Hamby SE,
Di Angelantonio E,
Assimes TL,
Bottinger EP,
Chambers JC,
Clarke R,
Palmer CNA,
Cubbon RM,
Ellinor P,
Ermel R,
Evangelou E,
Franks PW,
Grace C,
Gu D,
Hingorani AD,
Howson JMM,
Ingelsson E,
Kastrati A,
Kessler T,
Kyriakou T,
Lehtimäki T,
Lu X,
Lu Y,
März W,
McPherson R,
Metspalu A,
Pujades-Rodriguez M,
Ruusalepp A,
Schadt EE,
Schmidt AF,
Sweeting MJ,
Zalloua PA,
AlGhalayini K,
Keavney BD,
Kooner JS,
Loos RJF,
Patel RS,
Rutter MK,
Tomaszewski M,
Tzoulaki I,
Zeggini E,
Erdmann J,
Dedoussis G,
Björkegren JLM,
Schunkert H,
Farrall M,
Danesh J,
Samani NJ,
Watkins H,
Deloukas P
EPIC-CVD Consortium · CARDIoGRAMplusC4D and 1 more consortia
Nature genetics · 2017 · PMID 28714975
12 pages+
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney
Wain LV,
Vaez A,
Jansen R,
Joehanes R,
van der Most PJ,
Erzurumluoglu AM,
O'Reilly PF,
Cabrera CP,
Warren HR,
Rose LM,
Verwoert GC,
Hottenga JJ
and 239 more — show all
Strawbridge RJ,
Esko T,
Arking DE,
Hwang SJ,
Guo X,
Kutalik Z,
Trompet S,
Shrine N,
Teumer A,
Ried JS,
Bis JC,
Smith AV,
Amin N,
Nolte IM,
Lyytikäinen LP,
Mahajan A,
Wareham NJ,
Hofer E,
Joshi PK,
Kristiansson K,
Traglia M,
Havulinna AS,
Goel A,
Nalls MA,
Sõber S,
Vuckovic D,
Luan J,
Del Greco M F,
Ayers KL,
Marrugat J,
Ruggiero D,
Lopez LM,
Niiranen T,
Enroth S,
Jackson AU,
Nelson CP,
Huffman JE,
Zhang W,
Marten J,
Gandin I,
Harris SE,
Zemunik T,
Lu Y,
Evangelou E,
Shah N,
de Borst MH,
Mangino M,
Prins BP,
Campbell A,
Li-Gao R,
Chauhan G,
Oldmeadow C,
Abecasis G,
Abedi M,
Barbieri CM,
Barnes MR,
Batini C,
Beilby J,
Blake T,
Boehnke M,
Bottinger EP,
Braund PS,
Brown M,
Brumat M,
Campbell H,
Chambers JC,
Cocca M,
Collins F,
Connell J,
Cordell HJ,
Damman JJ,
Davies G,
de Geus EJ,
de Mutsert R,
Deelen J,
Demirkale Y,
Doney ASF,
Doney ASF,
Dörr M,
Farrall M,
Ferreira T,
Frånberg M,
Gao H,
Giedraitis V,
Gieger C,
Giulianini F,
Gow AJ,
Hamsten A,
Harris TB,
Hofman A,
Holliday EG,
Hui J,
Jarvelin MR,
Johansson Å,
Johnson AD,
Jousilahti P,
Jula A,
Kähönen M,
Kathiresan S,
Khaw KT,
Kolcic I,
Koskinen S,
Langenberg C,
Larson M,
Launer LJ,
Lehne B,
Liewald DCM,
Lin L,
Lind L,
Mach F,
Mamasoula C,
Menni C,
Menni C,
Mifsud B,
Milaneschi Y,
Morgan A,
Morris AD,
Morrison AC,
Munson PJ,
Nandakumar P,
Nguyen QT,
Nutile T,
Oldehinkel AJ,
Oostra BA,
Org E,
Org E,
Padmanabhan S,
Palotie A,
Paré G,
Pattie A,
Penninx BWJH,
Poulter N,
Pramstaller PP,
Raitakari OT,
Ren M,
Rice K,
Ridker PM,
Riese H,
Ripatti S,
Robino A,
Rotter JI,
Rudan I,
Saba Y,
Saint Pierre A,
Sala CF,
Sarin AP,
Schmidt R,
Scott R,
Seelen MA,
Shields DC,
Siscovick D,
Sorice R,
Stanton A,
Stott DJ,
Sundström J,
Swertz M,
Taylor KD,
Thom S,
Tzoulaki I,
Tzourio C,
Uitterlinden AG,
Uitterlinden AG,
Völker U,
Vollenweider P,
Wild S,
Willemsen G,
Wright AF,
Yao J,
Thériault S,
Conen D,
Attia J,
Sever P,
Debette S,
Mook-Kanamori DO,
Zeggini E,
Spector TD,
van der Harst P,
Palmer CNA,
Vergnaud AC,
Loos RJF,
Polasek O,
Polasek O,
Starr JM,
Girotto G,
Hayward C,
Kooner JS,
Lindgren CM,
Vitart V,
Samani NJ,
Tuomilehto J,
Gyllensten U,
Knekt P,
Deary IJ,
Ciullo M,
Elosua R,
Elosua R,
Keavney BD,
Hicks AA,
Scott RA,
Gasparini P,
Laan M,
Liu Y,
Watkins H,
Hartman CA,
Salomaa V,
Toniolo D,
Perola M,
Wilson JF,
Schmidt H,
Zhao JH,
Lehtimäki T,
Lehtimäki T,
van Duijn CM,
Gudnason V,
Psaty BM,
Peters A,
Rettig R,
James A,
Jukema JW,
Strachan DP,
Palmas W,
Metspalu A,
Ingelsson E,
Boomsma DI,
Franco OH,
Bochud M,
Newton-Cheh C,
Munroe PB,
Elliott P,
Chasman DI,
Chakravarti A,
Knight J,
Knight J,
Morris AP,
Levy D,
Tobin MD,
Snieder H,
Caulfield MJ,
Ehret GB
BIOS Consortium · Understanding Society Scientific Group
Hypertension (Dallas, Tex. : 1979) · 2017 · PMID 28739976
12 pages+
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis
Manousaki D,
Dudding T,
Haworth S,
Hsu YH,
Liu CT,
Medina-Gómez C,
Voortman T,
van der Velde N,
Melhus H,
Robinson-Cohen C,
Cousminer DL,
Nethander M
and 41 more — show all
Vandenput L,
Noordam R,
Forgetta V,
Greenwood CMT,
Biggs ML,
Psaty BM,
Rotter JI,
Zemel BS,
Mitchell JA,
Taylor B,
Lorentzon M,
Karlsson M,
Jaddoe VVW,
Tiemeier H,
Campos-Obando N,
Franco OH,
Utterlinden AG,
Broer L,
van Schoor NM,
Ham AC,
Ikram MA,
Karasik D,
de Mutsert R,
Rosendaal FR,
den Heijer M,
Wang TJ,
Lind L,
Orwoll ES,
Mook-Kanamori DO,
Michaëlsson K,
Kestenbaum B,
Ohlsson C,
Mellström D,
de Groot LCPGM,
Grant SFA,
Kiel DP,
Zillikens MC,
Rivadeneira F,
Sawcer S,
Timpson NJ,
Richards JB
American journal of human genetics · 2017 · PMID 28757204
12 pages+
Association analysis identifies 65 new breast cancer risk loci
Michailidou K,
Lindström S,
Dennis J,
Beesley J,
Hui S,
Kar S,
Lemaçon A,
Soucy P,
Glubb D,
Rostamianfar A,
Bolla MK,
Wang Q
and 347 more — show all
Tyrer J,
Dicks E,
Lee A,
Wang Z,
Allen J,
Keeman R,
Eilber U,
French JD,
Qing Chen X,
Fachal L,
McCue K,
McCart Reed AE,
Ghoussaini M,
Carroll JS,
Jiang X,
Finucane H,
Adams M,
Adank MA,
Ahsan H,
Aittomäki K,
Anton-Culver H,
Antonenkova NN,
Arndt V,
Aronson KJ,
Arun B,
Auer PL,
Bacot F,
Barrdahl M,
Baynes C,
Beckmann MW,
Behrens S,
Benitez J,
Bermisheva M,
Bernstein L,
Blomqvist C,
Bogdanova NV,
Bojesen SE,
Bonanni B,
Børresen-Dale AL,
Brand JS,
Brauch H,
Brennan P,
Brenner H,
Brinton L,
Broberg P,
Brock IW,
Broeks A,
Brooks-Wilson A,
Brucker SY,
Brüning T,
Burwinkel B,
Butterbach K,
Cai Q,
Cai H,
Caldés T,
Canzian F,
Carracedo A,
Carter BD,
Castelao JE,
Chan TL,
David Cheng TY,
Seng Chia K,
Choi JY,
Christiansen H,
Clarke CL,
Collée M,
Conroy DM,
Cordina-Duverger E,
Cornelissen S,
Cox DG,
Cox A,
Cross SS,
Cunningham JM,
Czene K,
Daly MB,
Devilee P,
Doheny KF,
Dörk T,
Dos-Santos-Silva I,
Dumont M,
Durcan L,
Dwek M,
Eccles DM,
Ekici AB,
Eliassen AH,
Ellberg C,
Elvira M,
Engel C,
Eriksson M,
Fasching PA,
Figueroa J,
Flesch-Janys D,
Fletcher O,
Flyger H,
Fritschi L,
Gaborieau V,
Gabrielson M,
Gago-Dominguez M,
Gao YT,
Gapstur SM,
García-Sáenz JA,
Gaudet MM,
Georgoulias V,
Giles GG,
Glendon G,
Goldberg MS,
Goldgar DE,
González-Neira A,
Grenaker Alnæs GI,
Grip M,
Gronwald J,
Grundy A,
Guénel P,
Haeberle L,
Hahnen E,
Haiman CA,
Håkansson N,
Hamann U,
Hamel N,
Hankinson S,
Harrington P,
Hart SN,
Hartikainen JM,
Hartman M,
Hein A,
Heyworth J,
Hicks B,
Hillemanns P,
Ho DN,
Hollestelle A,
Hooning MJ,
Hoover RN,
Hopper JL,
Hou MF,
Hsiung CN,
Huang G,
Humphreys K,
Ishiguro J,
Ito H,
Iwasaki M,
Iwata H,
Jakubowska A,
Janni W,
John EM,
Johnson N,
Jones K,
Jones M,
Jukkola-Vuorinen A,
Kaaks R,
Kabisch M,
Kaczmarek K,
Kang D,
Kasuga Y,
Kerin MJ,
Khan S,
Khusnutdinova E,
Kiiski JI,
Kim SW,
Knight JA,
Kosma VM,
Kristensen VN,
Krüger U,
Kwong A,
Lambrechts D,
Le Marchand L,
Lee E,
Lee MH,
Lee JW,
Neng Lee C,
Lejbkowicz F,
Li J,
Lilyquist J,
Lindblom A,
Lissowska J,
Lo WY,
Loibl S,
Long J,
Lophatananon A,
Lubinski J,
Luccarini C,
Lux MP,
Ma ESK,
MacInnis RJ,
Maishman T,
Makalic E,
Malone KE,
Kostovska IM,
Mannermaa A,
Manoukian S,
Manson JE,
Margolin S,
Mariapun S,
Martinez ME,
Matsuo K,
Mavroudis D,
McKay J,
McLean C,
Meijers-Heijboer H,
Meindl A,
Menéndez P,
Menon U,
Meyer J,
Miao H,
Miller N,
Taib NAM,
Muir K,
Mulligan AM,
Mulot C,
Neuhausen SL,
Nevanlinna H,
Neven P,
Nielsen SF,
Noh DY,
Nordestgaard BG,
Norman A,
Olopade OI,
Olson JE,
Olsson H,
Olswold C,
Orr N,
Pankratz VS,
Park SK,
Park-Simon TW,
Lloyd R,
Perez JIA,
Peterlongo P,
Peto J,
Phillips KA,
Pinchev M,
Plaseska-Karanfilska D,
Prentice R,
Presneau N,
Prokofyeva D,
Pugh E,
Pylkäs K,
Rack B,
Radice P,
Rahman N,
Rennert G,
Rennert HS,
Rhenius V,
Romero A,
Romm J,
Ruddy KJ,
Rüdiger T,
Rudolph A,
Ruebner M,
Rutgers EJT,
Saloustros E,
Sandler DP,
Sangrajrang S,
Sawyer EJ,
Schmidt DF,
Schmutzler RK,
Schneeweiss A,
Schoemaker MJ,
Schumacher F,
Schürmann P,
Scott RJ,
Scott C,
Seal S,
Seynaeve C,
Shah M,
Sharma P,
Shen CY,
Sheng G,
Sherman ME,
Shrubsole MJ,
Shu XO,
Smeets A,
Sohn C,
Southey MC,
Spinelli JJ,
Stegmaier C,
Stewart-Brown S,
Stone J,
Stram DO,
Surowy H,
Swerdlow A,
Tamimi R,
Taylor JA,
Tengström M,
Teo SH,
Beth Terry M,
Tessier DC,
Thanasitthichai S,
Thöne K,
Tollenaar RAEM,
Tomlinson I,
Tong L,
Torres D,
Truong T,
Tseng CC,
Tsugane S,
Ulmer HU,
Ursin G,
Untch M,
Vachon C,
van Asperen CJ,
Van Den Berg D,
van den Ouweland AMW,
van der Kolk L,
van der Luijt RB,
Vincent D,
Vollenweider J,
Waisfisz Q,
Wang-Gohrke S,
Weinberg CR,
Wendt C,
Whittemore AS,
Wildiers H,
Willett W,
Winqvist R,
Wolk A,
Wu AH,
Xia L,
Yamaji T,
Yang XR,
Har Yip C,
Yoo KY,
Yu JC,
Zheng W,
Zheng Y,
Zhu B,
Ziogas A,
Ziv E,
Lakhani SR,
Antoniou AC,
Droit A,
Andrulis IL,
Amos CI,
Couch FJ,
Pharoah PDP,
Chang-Claude J,
Hall P,
Hunter DJ,
Milne RL,
García-Closas M,
Schmidt MK,
Chanock SJ,
Dunning AM,
Edwards SL,
Bader GD,
Chenevix-Trench G,
Simard J,
Kraft P,
Easton DF
NBCS Collaborators · ABCTB Investigators and 1 more consortia
Nature · 2017 · PMID 29059683 · open access
12 pages+
Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks
Demenais F,
Margaritte-Jeannin P,
Barnes KC,
Cookson WOC,
Altmüller J,
Ang W,
Barr RG,
Beaty TH,
Becker AB,
Beilby J,
Bisgaard H,
Bjornsdottir US
and 163 more — show all
Bleecker E,
Bønnelykke K,
Boomsma DI,
Bouzigon E,
Brightling CE,
Brossard M,
Brusselle GG,
Burchard E,
Burkart KM,
Bush A,
Chan-Yeung M,
Chung KF,
Couto Alves A,
Curtin JA,
Custovic A,
Daley D,
de Jongste JC,
Del-Rio-Navarro BE,
Donohue KM,
Duijts L,
Eng C,
Eriksson JG,
Farrall M,
Fedorova Y,
Feenstra B,
Ferreira MA,
Freidin MB,
Gajdos Z,
Gauderman J,
Gehring U,
Geller F,
Genuneit J,
Gharib SA,
Gilliland F,
Granell R,
Graves PE,
Gudbjartsson DF,
Haahtela T,
Heckbert SR,
Heederik D,
Heinrich J,
Heliövaara M,
Henderson J,
Himes BE,
Hirose H,
Hirschhorn JN,
Hofman A,
Holt P,
Hottenga J,
Hudson TJ,
Hui J,
Imboden M,
Ivanov V,
Jaddoe VWV,
James A,
Janson C,
Jarvelin MR,
Jarvis D,
Jones G,
Jonsdottir I,
Jousilahti P,
Kabesch M,
Kähönen M,
Kantor DB,
Karunas AS,
Khusnutdinova E,
Koppelman GH,
Kozyrskyj AL,
Kreiner E,
Kubo M,
Kumar R,
Kumar A,
Kuokkanen M,
Lahousse L,
Laitinen T,
Laprise C,
Lathrop M,
Lau S,
Lee YA,
Lehtimäki T,
Letort S,
Levin AM,
Li G,
Liang L,
Loehr LR,
London SJ,
Loth DW,
Manichaikul A,
Marenholz I,
Martinez FJ,
Matheson MC,
Mathias RA,
Matsumoto K,
Mbarek H,
McArdle WL,
Melbye M,
Melén E,
Meyers D,
Michel S,
Mohamdi H,
Musk AW,
Myers RA,
Nieuwenhuis MAE,
Noguchi E,
O'Connor GT,
Ogorodova LM,
Palmer CD,
Palotie A,
Park JE,
Pennell CE,
Pershagen G,
Polonikov A,
Postma DS,
Probst-Hensch N,
Puzyrev VP,
Raby BA,
Raitakari OT,
Ramasamy A,
Rich SS,
Robertson CF,
Romieu I,
Salam MT,
Salomaa V,
Schlünssen V,
Scott R,
Selivanova PA,
Sigsgaard T,
Simpson A,
Siroux V,
Smith LJ,
Solodilova M,
Standl M,
Stefansson K,
Strachan DP,
Stricker BH,
Takahashi A,
Thompson PJ,
Thorleifsson G,
Thorsteinsdottir U,
Tiesler CMT,
Torgerson DG,
Tsunoda T,
Uitterlinden AG,
van der Valk RJP,
Vaysse A,
Vedantam S,
von Berg A,
von Mutius E,
Vonk JM,
Waage J,
Wareham NJ,
Weiss ST,
White WB,
Wickman M,
Widén E,
Willemsen G,
Williams LK,
Wouters IM,
Yang JJ,
Zhao JH,
Moffatt MF,
Ober C,
Nicolae DL
Australian Asthma Genetics Consortium (AAGC) collaborators
Nature genetics · 2018 · PMID 29273806 · open access
12 pages+
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
Turcot V,
Lu Y,
Highland HM,
Schurmann C,
Justice AE,
Fine RS,
Bradfield JP,
Esko T,
Giri A,
Graff M,
Guo X,
Hendricks AE
and 390 more — show all
Karaderi T,
Lempradl A,
Locke AE,
Mahajan A,
Marouli E,
Sivapalaratnam S,
Young KL,
Alfred T,
Feitosa MF,
Masca NGD,
Manning AK,
Medina-Gomez C,
Mudgal P,
Ng MCY,
Reiner AP,
Vedantam S,
Willems SM,
Winkler TW,
Abecasis G,
Aben KK,
Alam DS,
Alharthi SE,
Allison M,
Amouyel P,
Asselbergs FW,
Auer PL,
Balkau B,
Bang LE,
Barroso I,
Bastarache L,
Benn M,
Bergmann S,
Bielak LF,
Blüher M,
Boehnke M,
Boeing H,
Boerwinkle E,
Böger CA,
Bork-Jensen J,
Bots ML,
Bottinger EP,
Bowden DW,
Brandslund I,
Breen G,
Brilliant MH,
Broer L,
Brumat M,
Burt AA,
Butterworth AS,
Campbell PT,
Cappellani S,
Carey DJ,
Catamo E,
Caulfield MJ,
Chambers JC,
Chasman DI,
Chen YI,
Chowdhury R,
Christensen C,
Chu AY,
Cocca M,
Collins FS,
Cook JP,
Corley J,
Corominas Galbany J,
Cox AJ,
Crosslin DS,
Cuellar-Partida G,
D'Eustacchio A,
Danesh J,
Davies G,
Bakker PIW,
Groot MCH,
Mutsert R,
Deary IJ,
Dedoussis G,
Demerath EW,
Heijer M,
Hollander AI,
Ruijter HM,
Dennis JG,
Denny JC,
Di Angelantonio E,
Drenos F,
Du M,
Dubé MP,
Dunning AM,
Easton DF,
Edwards TL,
Ellinghaus D,
Ellinor PT,
Elliott P,
Evangelou E,
Farmaki AE,
Farooqi IS,
Faul JD,
Fauser S,
Feng S,
Ferrannini E,
Ferrieres J,
Florez JC,
Ford I,
Fornage M,
Franco OH,
Franke A,
Franks PW,
Friedrich N,
Frikke-Schmidt R,
Galesloot TE,
Gan W,
Gandin I,
Gasparini P,
Gibson J,
Giedraitis V,
Gjesing AP,
Gordon-Larsen P,
Gorski M,
Grabe HJ,
Grant SFA,
Grarup N,
Griffiths HL,
Grove ML,
Gudnason V,
Gustafsson S,
Haessler J,
Hakonarson H,
Hammerschlag AR,
Hansen T,
Harris KM,
Harris TB,
Hattersley AT,
Have CT,
Hayward C,
He L,
Heard-Costa NL,
Heath AC,
Heid IM,
Helgeland Ø,
Hernesniemi J,
Hewitt AW,
Holmen OL,
Hovingh GK,
Howson JMM,
Hu Y,
Huang PL,
Huffman JE,
Ikram MA,
Ingelsson E,
Jackson AU,
Jansson JH,
Jarvik GP,
Jensen GB,
Jia Y,
Johansson S,
Jørgensen ME,
Jørgensen T,
Jukema JW,
Kahali B,
Kahn RS,
Kähönen M,
Kamstrup PR,
Kanoni S,
Kaprio J,
Karaleftheri M,
Kardia SLR,
Karpe F,
Kathiresan S,
Kee F,
Kiemeney LA,
Kim E,
Kitajima H,
Komulainen P,
Kooner JS,
Kooperberg C,
Korhonen T,
Kovacs P,
Kuivaniemi H,
Kutalik Z,
Kuulasmaa K,
Kuusisto J,
Laakso M,
Lakka TA,
Lamparter D,
Lange EM,
Lange LA,
Langenberg C,
Larson EB,
Lee NR,
Lehtimäki T,
Lewis CE,
Li H,
Li J,
Li-Gao R,
Lin H,
Lin KH,
Lin LA,
Lin X,
Lind L,
Lindström J,
Linneberg A,
Liu CT,
Liu DJ,
Liu Y,
Lo KS,
Lophatananon A,
Lotery AJ,
Loukola A,
Luan J,
Lubitz SA,
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12 pages+
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23andMe Research Team
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12 pages+
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Nature genetics · 2018 · PMID 29942086
12 pages+
Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis
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Amaral AFS
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23andMe Research Team · AAGC collaborators
Nature genetics · 2018 · PMID 30013184
12 pages+
PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity
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Nature communications · 2018 · PMID 30046033 · open access
12 pages+
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function
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Nature communications · 2018 · PMID 30061609 · open access
12 pages+
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
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Million Veteran Program
Nature genetics · 2018 · PMID 30224653
12 pages+
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
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Nature genetics · 2018 · PMID 30297969
12 pages+
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation
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Lifelines Cohort Study
Nature communications · 2018 · PMID 30367059 · open access
12 pages+
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders
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LifeLines Cohort Study · CHARGE Inflammation Working Group
American journal of human genetics · 2018 · PMID 30388399
12 pages+
Questions about this list
Why is my paper here? I never gave you permission.
Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
cites your work, and links to the paper on PubMed — which is what a citation is.
Your title and author list come from Europe PMC, the same public record a library
catalogue uses.
Why are all the authors listed instead of "et al."?
Because a study that needed 622 people is a different kind of study from one that
needed four, and "et al." erases that. Twelve names show and the rest are one click
away. Everyone is searchable, including the 187th name on a consortium paper —
that person exists and may be looking for it.
My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
inconsistent across databases; where two people share a form of a name we cannot
separate them, and we would rather be corrected than guess.
My paper is not here. Does that mean you rejected it?
No. This catalogue is assembled from what a small team could read, and it is
thinnest outside European-ancestry cohorts. A paper is absent because nobody has got
to it, not because it was assessed and turned down.
Which pages rest on a paper?
Each row lists them, up to six, and links to each one. The count beside a row is
how many pages cite it in total.
How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
resting on it and disappears if that page stops — there is no separate list to
keep in step, because the citation lives on the page that makes the claim.