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Brambilla P.
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
Berndt SI,
Gustafsson S,
Mägi R,
Ganna A,
Wheeler E,
Feitosa MF,
Justice AE,
Monda KL,
Croteau-Chonka DC,
Day FR,
Esko T,
Fall T
and 310 more — show all
Ferreira T,
Gentilini D,
Jackson AU,
Luan J,
Randall JC,
Vedantam S,
Willer CJ,
Winkler TW,
Wood AR,
Workalemahu T,
Hu YJ,
Lee SH,
Liang L,
Lin DY,
Min JL,
Neale BM,
Thorleifsson G,
Yang J,
Albrecht E,
Amin N,
Bragg-Gresham JL,
Cadby G,
den Heijer M,
Eklund N,
Fischer K,
Goel A,
Hottenga JJ,
Huffman JE,
Jarick I,
Johansson Å,
Johnson T,
Kanoni S,
Kleber ME,
König IR,
Kristiansson K,
Kutalik Z,
Lamina C,
Lecoeur C,
Li G,
Mangino M,
McArdle WL,
Medina-Gomez C,
Müller-Nurasyid M,
Ngwa JS,
Nolte IM,
Paternoster L,
Pechlivanis S,
Perola M,
Peters MJ,
Preuss M,
Rose LM,
Shi J,
Shungin D,
Smith AV,
Strawbridge RJ,
Surakka I,
Teumer A,
Trip MD,
Tyrer J,
Van Vliet-Ostaptchouk JV,
Vandenput L,
Waite LL,
Zhao JH,
Absher D,
Asselbergs FW,
Atalay M,
Attwood AP,
Balmforth AJ,
Basart H,
Beilby J,
Bonnycastle LL,
Brambilla P,
Bruinenberg M,
Campbell H,
Chasman DI,
Chines PS,
Collins FS,
Connell JM,
Cookson WO,
de Faire U,
de Vegt F,
Dei M,
Dimitriou M,
Edkins S,
Estrada K,
Evans DM,
Farrall M,
Ferrario MM,
Ferrières J,
Franke L,
Frau F,
Gejman PV,
Grallert H,
Grönberg H,
Gudnason V,
Hall AS,
Hall P,
Hartikainen AL,
Hayward C,
Heard-Costa NL,
Heath AC,
Hebebrand J,
Homuth G,
Hu FB,
Hunt SE,
Hyppönen E,
Iribarren C,
Jacobs KB,
Jansson JO,
Jula A,
Kähönen M,
Kathiresan S,
Kee F,
Khaw KT,
Kivimäki M,
Koenig W,
Kraja AT,
Kumari M,
Kuulasmaa K,
Kuusisto J,
Laitinen JH,
Lakka TA,
Langenberg C,
Launer LJ,
Lind L,
Lindström J,
Liu J,
Liuzzi A,
Lokki ML,
Lorentzon M,
Madden PA,
Magnusson PK,
Manunta P,
Marek D,
März W,
Mateo Leach I,
McKnight B,
Medland SE,
Mihailov E,
Milani L,
Montgomery GW,
Mooser V,
Mühleisen TW,
Munroe PB,
Musk AW,
Narisu N,
Navis G,
Nicholson G,
Nohr EA,
Ong KK,
Oostra BA,
Palmer CN,
Palotie A,
Peden JF,
Pedersen N,
Peters A,
Polasek O,
Pouta A,
Pramstaller PP,
Prokopenko I,
Pütter C,
Radhakrishnan A,
Raitakari O,
Rendon A,
Rivadeneira F,
Rudan I,
Saaristo TE,
Sambrook JG,
Sanders AR,
Sanna S,
Saramies J,
Schipf S,
Schreiber S,
Schunkert H,
Shin SY,
Signorini S,
Sinisalo J,
Skrobek B,
Soranzo N,
Stančáková A,
Stark K,
Stephens JC,
Stirrups K,
Stolk RP,
Stumvoll M,
Swift AJ,
Theodoraki EV,
Thorand B,
Tregouet DA,
Tremoli E,
Van der Klauw MM,
van Meurs JB,
Vermeulen SH,
Viikari J,
Virtamo J,
Vitart V,
Waeber G,
Wang Z,
Widén E,
Wild SH,
Willemsen G,
Winkelmann BR,
Witteman JC,
Wolffenbuttel BH,
Wong A,
Wright AF,
Zillikens MC,
Amouyel P,
Boehm BO,
Boerwinkle E,
Boomsma DI,
Caulfield MJ,
Chanock SJ,
Cupples LA,
Cusi D,
Dedoussis GV,
Erdmann J,
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Franks PW,
Froguel P,
Gieger C,
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Hamsten A,
Harris TB,
Hengstenberg C,
Hicks AA,
Hingorani A,
Hinney A,
Hofman A,
Hovingh KG,
Hveem K,
Illig T,
Jarvelin MR,
Jöckel KH,
Keinanen-Kiukaanniemi SM,
Kiemeney LA,
Kuh D,
Laakso M,
Lehtimäki T,
Levinson DF,
Martin NG,
Metspalu A,
Morris AD,
Nieminen MS,
Njølstad I,
Ohlsson C,
Oldehinkel AJ,
Ouwehand WH,
Palmer LJ,
Penninx B,
Power C,
Province MA,
Psaty BM,
Qi L,
Rauramaa R,
Ridker PM,
Ripatti S,
Salomaa V,
Samani NJ,
Snieder H,
Sørensen TI,
Spector TD,
Stefansson K,
Tönjes A,
Tuomilehto J,
Uitterlinden AG,
Uusitupa M,
van der Harst P,
Vollenweider P,
Wallaschofski H,
Wareham NJ,
Watkins H,
Wichmann HE,
Wilson JF,
Abecasis GR,
Assimes TL,
Barroso I,
Boehnke M,
Borecki IB,
Deloukas P,
Fox CS,
Frayling T,
Groop LC,
Haritunian T,
Heid IM,
Hunter D,
Kaplan RC,
Karpe F,
Moffatt MF,
Mohlke KL,
O'Connell JR,
Pawitan Y,
Schadt EE,
Schlessinger D,
Steinthorsdottir V,
Strachan DP,
Thorsteinsdottir U,
van Duijn CM,
Visscher PM,
Di Blasio AM,
Hirschhorn JN,
Lindgren CM,
Morris AP,
Meyre D,
Scherag A,
McCarthy MI,
Speliotes EK,
North KE,
Loos RJ,
Ingelsson E
Nature genetics · 2013 · PMID 23563607 · open access
12 pages+
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
Beecham AH,
Patsopoulos NA,
Xifara DK,
Davis MF,
Kemppinen A,
Cotsapas C,
Shah TS,
Spencer C,
Booth D,
Goris A,
Oturai A,
Saarela J
and 181 more — show all
Fontaine B,
Hemmer B,
Martin C,
Zipp F,
D'Alfonso S,
Martinelli-Boneschi F,
Taylor B,
Harbo HF,
Kockum I,
Hillert J,
Olsson T,
Ban M,
Oksenberg JR,
Hintzen R,
Barcellos LF,
Agliardi C,
Alfredsson L,
Alizadeh M,
Anderson C,
Andrews R,
Søndergaard HB,
Baker A,
Band G,
Baranzini SE,
Barizzone N,
Barrett J,
Bellenguez C,
Bergamaschi L,
Bernardinelli L,
Berthele A,
Biberacher V,
Binder TM,
Blackburn H,
Bomfim IL,
Brambilla P,
Broadley S,
Brochet B,
Brundin L,
Buck D,
Butzkueven H,
Caillier SJ,
Camu W,
Carpentier W,
Cavalla P,
Celius EG,
Coman I,
Comi G,
Corrado L,
Cosemans L,
Cournu-Rebeix I,
Cree BA,
Cusi D,
Damotte V,
Defer G,
Delgado SR,
Deloukas P,
di Sapio A,
Dilthey AT,
Donnelly P,
Dubois B,
Duddy M,
Edkins S,
Elovaara I,
Esposito F,
Evangelou N,
Fiddes B,
Field J,
Franke A,
Freeman C,
Frohlich IY,
Galimberti D,
Gieger C,
Gourraud PA,
Graetz C,
Graham A,
Grummel V,
Guaschino C,
Hadjixenofontos A,
Hakonarson H,
Halfpenny C,
Hall G,
Hall P,
Hamsten A,
Harley J,
Harrower T,
Hawkins C,
Hellenthal G,
Hillier C,
Hobart J,
Hoshi M,
Hunt SE,
Jagodic M,
Jelčić I,
Jochim A,
Kendall B,
Kermode A,
Kilpatrick T,
Koivisto K,
Konidari I,
Korn T,
Kronsbein H,
Langford C,
Larsson M,
Lathrop M,
Lebrun-Frenay C,
Lechner-Scott J,
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Leone MA,
Leppä V,
Liberatore G,
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Lill CM,
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Link J,
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Lycke J,
Macciardi F,
Männistö S,
Manrique CP,
Martin R,
Martinelli V,
Mason D,
Mazibrada G,
McCabe C,
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Moutsianas L,
Myhr KM,
Nagels G,
Nicholas R,
Nilsson P,
Piehl F,
Pirinen M,
Price SE,
Quach H,
Reunanen M,
Robberecht W,
Robertson NP,
Rodegher M,
Rog D,
Salvetti M,
Schnetz-Boutaud NC,
Sellebjerg F,
Selter RC,
Schaefer C,
Shaunak S,
Shen L,
Shields S,
Siffrin V,
Slee M,
Sorensen PS,
Sorosina M,
Sospedra M,
Spurkland A,
Strange A,
Sundqvist E,
Thijs V,
Thorpe J,
Ticca A,
Tienari P,
van Duijn C,
Visser EM,
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Westerlind H,
Wiley JS,
Wilkins A,
Wilson JF,
Winkelmann J,
Zajicek J,
Zindler E,
Haines JL,
Pericak-Vance MA,
Ivinson AJ,
Stewart G,
Hafler D,
Hauser SL,
Compston A,
McVean G,
De Jager P,
Sawcer SJ,
McCauley JL
International Multiple Sclerosis Genetics Consortium (IMSGC) · Wellcome Trust Case Control Consortium 2 (WTCCC2) and 1 more consortia
Nature genetics · 2013 · PMID 24076602 · open access
12 pages+
Discovery and refinement of loci associated with lipid levels
Willer CJ,
Schmidt EM,
Sengupta S,
Peloso GM,
Gustafsson S,
Kanoni S,
Ganna A,
Chen J,
Buchkovich ML,
Mora S,
Beckmann JS,
Bragg-Gresham JL
and 247 more — show all
Chang HY,
Demirkan A,
Den Hertog HM,
Do R,
Donnelly LA,
Ehret GB,
Esko T,
Feitosa MF,
Ferreira T,
Fischer K,
Fontanillas P,
Fraser RM,
Freitag DF,
Gurdasani D,
Heikkilä K,
Hyppönen E,
Isaacs A,
Jackson AU,
Johansson Å,
Johnson T,
Kaakinen M,
Kettunen J,
Kleber ME,
Li X,
Luan J,
Lyytikäinen LP,
Magnusson PKE,
Mangino M,
Mihailov E,
Montasser ME,
Müller-Nurasyid M,
Nolte IM,
O'Connell JR,
Palmer CD,
Perola M,
Petersen AK,
Sanna S,
Saxena R,
Service SK,
Shah S,
Shungin D,
Sidore C,
Song C,
Strawbridge RJ,
Surakka I,
Tanaka T,
Teslovich TM,
Thorleifsson G,
Van den Herik EG,
Voight BF,
Volcik KA,
Waite LL,
Wong A,
Wu Y,
Zhang W,
Absher D,
Asiki G,
Barroso I,
Been LF,
Bolton JL,
Bonnycastle LL,
Brambilla P,
Burnett MS,
Cesana G,
Dimitriou M,
Doney ASF,
Döring A,
Elliott P,
Epstein SE,
Ingi Eyjolfsson G,
Gigante B,
Goodarzi MO,
Grallert H,
Gravito ML,
Groves CJ,
Hallmans G,
Hartikainen AL,
Hayward C,
Hernandez D,
Hicks AA,
Holm H,
Hung YJ,
Illig T,
Jones MR,
Kaleebu P,
Kastelein JJP,
Khaw KT,
Kim E,
Klopp N,
Komulainen P,
Kumari M,
Langenberg C,
Lehtimäki T,
Lin SY,
Lindström J,
Loos RJF,
Mach F,
McArdle WL,
Meisinger C,
Mitchell BD,
Müller G,
Nagaraja R,
Narisu N,
Nieminen TVM,
Nsubuga RN,
Olafsson I,
Ong KK,
Palotie A,
Papamarkou T,
Pomilla C,
Pouta A,
Rader DJ,
Reilly MP,
Ridker PM,
Rivadeneira F,
Rudan I,
Ruokonen A,
Samani N,
Scharnagl H,
Seeley J,
Silander K,
Stančáková A,
Stirrups K,
Swift AJ,
Tiret L,
Uitterlinden AG,
van Pelt LJ,
Vedantam S,
Wainwright N,
Wijmenga C,
Wild SH,
Willemsen G,
Wilsgaard T,
Wilson JF,
Young EH,
Zhao JH,
Adair LS,
Arveiler D,
Assimes TL,
Bandinelli S,
Bennett F,
Bochud M,
Boehm BO,
Boomsma DI,
Borecki IB,
Bornstein SR,
Bovet P,
Burnier M,
Campbell H,
Chakravarti A,
Chambers JC,
Chen YI,
Collins FS,
Cooper RS,
Danesh J,
Dedoussis G,
de Faire U,
Feranil AB,
Ferrières J,
Ferrucci L,
Freimer NB,
Gieger C,
Groop LC,
Gudnason V,
Gyllensten U,
Hamsten A,
Harris TB,
Hingorani A,
Hirschhorn JN,
Hofman A,
Hovingh GK,
Hsiung CA,
Humphries SE,
Hunt SC,
Hveem K,
Iribarren C,
Järvelin MR,
Jula A,
Kähönen M,
Kaprio J,
Kesäniemi A,
Kivimaki M,
Kooner JS,
Koudstaal PJ,
Krauss RM,
Kuh D,
Kuusisto J,
Kyvik KO,
Laakso M,
Lakka TA,
Lind L,
Lindgren CM,
Martin NG,
März W,
McCarthy MI,
McKenzie CA,
Meneton P,
Metspalu A,
Moilanen L,
Morris AD,
Munroe PB,
Njølstad I,
Pedersen NL,
Power C,
Pramstaller PP,
Price JF,
Psaty BM,
Quertermous T,
Rauramaa R,
Saleheen D,
Salomaa V,
Sanghera DK,
Saramies J,
Schwarz PEH,
Sheu WH,
Shuldiner AR,
Siegbahn A,
Spector TD,
Stefansson K,
Strachan DP,
Tayo BO,
Tremoli E,
Tuomilehto J,
Uusitupa M,
van Duijn CM,
Vollenweider P,
Wallentin L,
Wareham NJ,
Whitfield JB,
Wolffenbuttel BHR,
Ordovas JM,
Boerwinkle E,
Palmer CNA,
Thorsteinsdottir U,
Chasman DI,
Rotter JI,
Franks PW,
Ripatti S,
Cupples LA,
Sandhu MS,
Rich SS,
Boehnke M,
Deloukas P,
Kathiresan S,
Mohlke KL,
Ingelsson E,
Abecasis GR
Global Lipids Genetics Consortium
Nature genetics · 2013 · PMID 24097068 · open access
12 pages+
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
and 433 more — show all
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,
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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,
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Verweij N,
Vonk JM,
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Wennauer R,
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Willenborg C,
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Campbell H,
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Chakravarti A,
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Crawford DC,
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Farrall M,
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Ford I,
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Gansevoort RT,
Gejman PV,
Gieger C,
Golay A,
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Gudnason V,
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Hall AS,
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Hengstenberg C,
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Hindorff LA,
Hingorani AD,
Hofman A,
Hovingh GK,
Humphries SE,
Hunt SC,
Hypponen E,
Jacobs KB,
Jarvelin MR,
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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,
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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,
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Electronic Medical Records and Genomics (eMEMERGEGE) Consortium · MIGen Consortium and 2 more consortia
Nature genetics · 2014 · PMID 25282103 · open access
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.