For researchers
Is your paper here?
2,657 papers hold this site up. Every variant and condition page names
the research it was written from, and this is that list, gathered from the pages themselves.
Search your name, your journal, or a PMID.
11 matches for
Dei M.
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,
Eriksson JG,
Franks PW,
Froguel P,
Gieger C,
Gyllensten U,
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+
Complex genetic signatures in immune cells underlie autoimmunity and inform therapy
Orrù V,
Steri M,
Sidore C,
Marongiu M,
Serra V,
Olla S,
Sole G,
Lai S,
Dei M,
Mulas A,
Virdis F,
Piras MG
and 16 more — show all
Lobina M,
Marongiu M,
Pitzalis M,
Deidda F,
Loizedda A,
Onano S,
Zoledziewska M,
Sawcer S,
Devoto M,
Gorospe M,
Abecasis GR,
Floris M,
Pala M,
Schlessinger D,
Fiorillo E,
Cucca F
Nature genetics · 2020 · PMID 32929287
12 pages+
Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways
Soranzo N,
Sanna S,
Wheeler E,
Gieger C,
Radke D,
Dupuis J,
Bouatia-Naji N,
Langenberg C,
Prokopenko I,
Stolerman E,
Sandhu MS,
Heeney MM
and 165 more — show all
Devaney JM,
Reilly MP,
Ricketts SL,
Stewart AF,
Voight BF,
Willenborg C,
Wright B,
Altshuler D,
Arking D,
Balkau B,
Barnes D,
Boerwinkle E,
Böhm B,
Bonnefond A,
Bonnycastle LL,
Boomsma DI,
Bornstein SR,
Böttcher Y,
Bumpstead S,
Burnett-Miller MS,
Campbell H,
Cao A,
Chambers J,
Clark R,
Collins FS,
Coresh J,
de Geus EJ,
Dei M,
Deloukas P,
Döring A,
Egan JM,
Elosua R,
Ferrucci L,
Forouhi N,
Fox CS,
Franklin C,
Franzosi MG,
Gallina S,
Goel A,
Graessler J,
Grallert H,
Greinacher A,
Hadley D,
Hall A,
Hamsten A,
Hayward C,
Heath S,
Herder C,
Homuth G,
Hottenga JJ,
Hunter-Merrill R,
Illig T,
Jackson AU,
Jula A,
Kleber M,
Knouff CW,
Kong A,
Kooner J,
Köttgen A,
Kovacs P,
Krohn K,
Kühnel B,
Kuusisto J,
Laakso M,
Lathrop M,
Lecoeur C,
Li M,
Li M,
Loos RJ,
Luan J,
Lyssenko V,
Mägi R,
Magnusson PK,
Mälarstig A,
Mangino M,
Martínez-Larrad MT,
März W,
McArdle WL,
McPherson R,
Meisinger C,
Meitinger T,
Melander O,
Mohlke KL,
Mooser VE,
Morken MA,
Narisu N,
Nathan DM,
Nauck M,
O'Donnell C,
Oexle K,
Olla N,
Pankow JS,
Payne F,
Peden JF,
Pedersen NL,
Peltonen L,
Perola M,
Polasek O,
Porcu E,
Rader DJ,
Rathmann W,
Ripatti S,
Rocheleau G,
Roden M,
Rudan I,
Salomaa V,
Saxena R,
Schlessinger D,
Schunkert H,
Schwarz P,
Seedorf U,
Selvin E,
Serrano-Ríos M,
Shrader P,
Silveira A,
Siscovick D,
Song K,
Spector TD,
Stefansson K,
Steinthorsdottir V,
Strachan DP,
Strawbridge R,
Stumvoll M,
Surakka I,
Swift AJ,
Tanaka T,
Teumer A,
Thorleifsson G,
Thorsteinsdottir U,
Tönjes A,
Usala G,
Vitart V,
Völzke H,
Wallaschofski H,
Waterworth DM,
Watkins H,
Wichmann HE,
Wild SH,
Willemsen G,
Williams GH,
Wilson JF,
Winkelmann J,
Wright AF,
Zabena C,
Zhao JH,
Epstein SE,
Erdmann J,
Hakonarson HH,
Kathiresan S,
Khaw KT,
Roberts R,
Samani NJ,
Fleming MD,
Sladek R,
Abecasis G,
Boehnke M,
Froguel P,
Groop L,
McCarthy MI,
Kao WH,
Florez JC,
Uda M,
Wareham NJ,
Barroso I,
Meigs JB
WTCCC
Diabetes · 2010 · PMID 20858683 · open access
5 pages
Common variants at ten loci modulate the QT interval duration in the QTSCD Study
Pfeufer A,
Sanna S,
Arking DE,
Müller M,
Gateva V,
Fuchsberger C,
Ehret GB,
Orrú M,
Pattaro C,
Köttgen A,
Perz S,
Usala G
and 32 more — show all
Barbalic M,
Li M,
Pütz B,
Scuteri A,
Prineas RJ,
Sinner MF,
Gieger C,
Najjar SS,
Kao WH,
Mühleisen TW,
Dei M,
Happle C,
Möhlenkamp S,
Crisponi L,
Erbel R,
Jöckel KH,
Naitza S,
Steinbeck G,
Marroni F,
Hicks AA,
Lakatta E,
Müller-Myhsok B,
Pramstaller PP,
Wichmann HE,
Schlessinger D,
Boerwinkle E,
Meitinger T,
Uda M,
Coresh J,
Kääb S,
Abecasis GR,
Chakravarti A
Nature genetics · 2009 · PMID 19305409
4 pages
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
Heid IM,
Jackson AU,
Randall JC,
Winkler TW,
Qi L,
Steinthorsdottir V,
Thorleifsson G,
Zillikens MC,
Speliotes EK,
Mägi R,
Workalemahu T,
White CC
and 290 more — show all
Bouatia-Naji N,
Harris TB,
Berndt SI,
Ingelsson E,
Willer CJ,
Weedon MN,
Luan J,
Vedantam S,
Esko T,
Kilpeläinen TO,
Kutalik Z,
Li S,
Monda KL,
Dixon AL,
Holmes CC,
Kaplan LM,
Liang L,
Min JL,
Moffatt MF,
Molony C,
Nicholson G,
Schadt EE,
Zondervan KT,
Feitosa MF,
Ferreira T,
Lango Allen H,
Weyant RJ,
Wheeler E,
Wood AR,
Estrada K,
Goddard ME,
Lettre G,
Mangino M,
Nyholt DR,
Purcell S,
Smith AV,
Visscher PM,
Yang J,
McCarroll SA,
Nemesh J,
Voight BF,
Absher D,
Amin N,
Aspelund T,
Coin L,
Glazer NL,
Hayward C,
Heard-Costa NL,
Hottenga JJ,
Johansson A,
Johnson T,
Kaakinen M,
Kapur K,
Ketkar S,
Knowles JW,
Kraft P,
Kraja AT,
Lamina C,
Leitzmann MF,
McKnight B,
Morris AP,
Ong KK,
Perry JR,
Peters MJ,
Polasek O,
Prokopenko I,
Rayner NW,
Ripatti S,
Rivadeneira F,
Robertson NR,
Sanna S,
Sovio U,
Surakka I,
Teumer A,
van Wingerden S,
Vitart V,
Zhao JH,
Cavalcanti-Proença C,
Chines PS,
Fisher E,
Kulzer JR,
Lecoeur C,
Narisu N,
Sandholt C,
Scott LJ,
Silander K,
Stark K,
Tammesoo ML,
Teslovich TM,
Timpson NJ,
Watanabe RM,
Welch R,
Chasman DI,
Cooper MN,
Jansson JO,
Kettunen J,
Lawrence RW,
Pellikka N,
Perola M,
Vandenput L,
Alavere H,
Almgren P,
Atwood LD,
Bennett AJ,
Biffar R,
Bonnycastle LL,
Bornstein SR,
Buchanan TA,
Campbell H,
Day IN,
Dei M,
Dörr M,
Elliott P,
Erdos MR,
Eriksson JG,
Freimer NB,
Fu M,
Gaget S,
Geus EJ,
Gjesing AP,
Grallert H,
Grässler J,
Groves CJ,
Guiducci C,
Hartikainen AL,
Hassanali N,
Havulinna AS,
Herzig KH,
Hicks AA,
Hui J,
Igl W,
Jousilahti P,
Jula A,
Kajantie E,
Kinnunen L,
Kolcic I,
Koskinen S,
Kovacs P,
Kroemer HK,
Krzelj V,
Kuusisto J,
Kvaloy K,
Laitinen J,
Lantieri O,
Lathrop GM,
Lokki ML,
Luben RN,
Ludwig B,
McArdle WL,
McCarthy A,
Morken MA,
Nelis M,
Neville MJ,
Paré G,
Parker AN,
Peden JF,
Pichler I,
Pietiläinen KH,
Platou CG,
Pouta A,
Ridderstråle M,
Samani NJ,
Saramies J,
Sinisalo J,
Smit JH,
Strawbridge RJ,
Stringham HM,
Swift AJ,
Teder-Laving M,
Thomson B,
Usala G,
van Meurs JB,
van Ommen GJ,
Vatin V,
Volpato CB,
Wallaschofski H,
Walters GB,
Widen E,
Wild SH,
Willemsen G,
Witte DR,
Zgaga L,
Zitting P,
Beilby JP,
James AL,
James AL,
Kähönen M,
Lehtimäki T,
Nieminen MS,
Ohlsson C,
Palmer LJ,
Raitakari O,
Ridker PM,
Stumvoll M,
Tönjes A,
Viikari J,
Balkau B,
Ben-Shlomo Y,
Bergman RN,
Boeing H,
Smith GD,
Ebrahim S,
Froguel P,
Hansen T,
Hengstenberg C,
Hveem K,
Isomaa B,
Jørgensen T,
Karpe F,
Khaw KT,
Laakso M,
Lawlor DA,
Marre M,
Meitinger T,
Metspalu A,
Midthjell K,
Pedersen O,
Salomaa V,
Schwarz PE,
Schwarz PE,
Tuomi T,
Tuomilehto J,
Valle TT,
Wareham NJ,
Arnold AM,
Beckmann JS,
Bergmann S,
Boerwinkle E,
Boomsma DI,
Caulfield MJ,
Collins FS,
Eiriksdottir G,
Gudnason V,
Gyllensten U,
Hamsten A,
Hattersley AT,
Hofman A,
Hu FB,
Illig T,
Iribarren C,
Jarvelin MR,
Kao WH,
Kaprio J,
Launer LJ,
Munroe PB,
Oostra B,
Penninx BW,
Pramstaller PP,
Psaty BM,
Quertermous T,
Rissanen A,
Rudan I,
Shuldiner AR,
Soranzo N,
Spector TD,
Syvanen AC,
Uda M,
Uitterlinden A,
Völzke H,
Vollenweider P,
Wilson JF,
Witteman JC,
Wright AF,
Abecasis GR,
Boehnke M,
Borecki IB,
Deloukas P,
Frayling TM,
Groop LC,
Haritunians T,
Hunter DJ,
Kaplan RC,
North KE,
O'Connell JR,
Peltonen L,
Schlessinger D,
Strachan DP,
Hirschhorn JN,
Assimes TL,
Wichmann HE,
Thorsteinsdottir U,
van Duijn CM,
Stefansson K,
Cupples LA,
Loos RJ,
Barroso I,
McCarthy MI,
Fox CS,
Mohlke KL,
Lindgren CM
MAGIC
Nature genetics · 2010 · PMID 20935629
3 pages
Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits
Scuteri A,
Sanna S,
Chen WM,
Uda M,
Albai G,
Strait J,
Najjar S,
Nagaraja R,
Orrú M,
Usala G,
Dei M,
Lai S
and 13 more — show all
Maschio A,
Busonero F,
Mulas A,
Ehret GB,
Fink AA,
Weder AB,
Cooper RS,
Galan P,
Chakravarti A,
Schlessinger D,
Cao A,
Lakatta E,
Abecasis GR
PLoS genetics · 2007 · PMID 17658951 · open access
2 pages
The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts
Li S,
Sanna S,
Maschio A,
Busonero F,
Usala G,
Mulas A,
Lai S,
Dei M,
Orrù M,
Albai G,
Bandinelli S,
Schlessinger D
and 12 more — show all
Lakatta E,
Scuteri A,
Najjar SS,
Guralnik J,
Naitza S,
Crisponi L,
Cao A,
Abecasis G,
Ferrucci L,
Uda M,
Chen WM,
Nagaraja R
PLoS genetics · 2007 · PMID 17997608 · open access
2 pages
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia
Uda M,
Galanello R,
Sanna S,
Lettre G,
Sankaran VG,
Chen W,
Usala G,
Busonero F,
Maschio A,
Albai G,
Piras MG,
Sestu N
and 18 more — show all
Lai S,
Dei M,
Mulas A,
Crisponi L,
Naitza S,
Asunis I,
Deiana M,
Nagaraja R,
Perseu L,
Satta S,
Cipollina MD,
Sollaino C,
Moi P,
Hirschhorn JN,
Orkin SH,
Abecasis GR,
Schlessinger D,
Cao A
Proceedings of the National Academy of Sciences of the United States of America · 2008 · PMID 18245381
2 pages
Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia
Sanna S,
Busonero F,
Maschio A,
McArdle PF,
Usala G,
Dei M,
Lai S,
Mulas A,
Piras MG,
Perseu L,
Masala M,
Marongiu M
and 8 more — show all
Human molecular genetics · 2009 · PMID 19419973
1 page
Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis
Sanna S,
Pitzalis M,
Zoledziewska M,
Zara I,
Sidore C,
Murru R,
Whalen MB,
Busonero F,
Maschio A,
Costa G,
Melis MC,
Deidda F
and 30 more — show all
Poddie F,
Morelli L,
Farina G,
Li Y,
Dei M,
Lai S,
Mulas A,
Cuccuru G,
Porcu E,
Liang L,
Zavattari P,
Moi L,
Deriu E,
Urru MF,
Bajorek M,
Satta MA,
Cocco E,
Ferrigno P,
Sotgiu S,
Pugliatti M,
Traccis S,
Angius A,
Angius A,
Melis M,
Rosati G,
Abecasis GR,
Uda M,
Marrosu MG,
Schlessinger D,
Cucca F
Nature genetics · 2010 · PMID 20453840
1 page
Overexpression of the Cytokine BAFF and Autoimmunity Risk
Steri M,
Orrù V,
Idda ML,
Pitzalis M,
Pala M,
Zara I,
Sidore C,
Faà V,
Floris M,
Deiana M,
Asunis I,
Porcu E
and 69 more — show all
Mulas A,
Piras MG,
Lobina M,
Lai S,
Marongiu M,
Serra V,
Marongiu M,
Sole G,
Busonero F,
Maschio A,
Cusano R,
Cuccuru G,
Deidda F,
Poddie F,
Farina G,
Dei M,
Virdis F,
Olla S,
Satta MA,
Pani M,
Delitala A,
Cocco E,
Frau J,
Coghe G,
Lorefice L,
Fenu G,
Ferrigno P,
Ban M,
Barizzone N,
Leone M,
Guerini FR,
Piga M,
Firinu D,
Kockum I,
Lima Bomfim I,
Olsson T,
Alfredsson L,
Suarez A,
Carreira PE,
Castillo-Palma MJ,
Marcus JH,
Congia M,
Angius A,
Melis M,
Gonzalez A,
Alarcón Riquelme ME,
da Silva BM,
Marchini M,
Danieli MG,
Del Giacco S,
Mathieu A,
Pani A,
Montgomery SB,
Rosati G,
Hillert J,
Sawcer S,
D'Alfonso S,
Todd JA,
Novembre J,
Abecasis GR,
Whalen MB,
Marrosu MG,
Meloni A,
Sanna S,
Gorospe M,
Schlessinger D,
Fiorillo E,
Zoledziewska M,
Cucca F
The New England journal of medicine · 2017 · PMID 28445677
1 page
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.