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2,671 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.
10 matches for
Lee MK.
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function
Wyss AB,
Sofer T,
Lee MK,
Terzikhan N,
Nguyen JN,
Lahousse L,
Latourelle JC,
Smith AV,
Bartz TM,
Feitosa MF,
Gao W,
Ahluwalia TS
and 91 more — show all
Tang W,
Oldmeadow C,
Duan Q,
de Jong K,
Wojczynski MK,
Wang XQ,
Noordam R,
Hartwig FP,
Jackson VE,
Wang T,
Obeidat M,
Hobbs BD,
Huan T,
Gui H,
Parker MM,
Hu D,
Mogil LS,
Kichaev G,
Jin J,
Graff M,
Harris TB,
Kalhan R,
Heckbert SR,
Paternoster L,
Burkart KM,
Liu Y,
Holliday EG,
Wilson JG,
Vonk JM,
Sanders JL,
Barr RG,
de Mutsert R,
Menezes AMB,
Adams HHH,
van den Berge M,
Joehanes R,
Levin AM,
Liberto J,
Launer LJ,
Morrison AC,
Sitlani CM,
Celedón JC,
Kritchevsky SB,
Scott RJ,
Christensen K,
Rotter JI,
Bonten TN,
Wehrmeister FC,
Bossé Y,
Xiao S,
Oh S,
Franceschini N,
Brody JA,
Kaplan RC,
Lohman K,
McEvoy M,
Province MA,
Rosendaal FR,
Taylor KD,
Nickle DC,
Williams LK,
Burchard EG,
Wheeler HE,
Wheeler HE,
Sin DD,
Gudnason V,
North KE,
Fornage M,
Psaty BM,
Myers RH,
O'Connor G,
Hansen T,
Laurie CC,
Cassano PA,
Sung J,
Kim WJ,
Attia JR,
Lange L,
Boezen HM,
Thyagarajan B,
Rich SS,
Mook-Kanamori DO,
Horta BL,
Uitterlinden AG,
Im HK,
Cho MH,
Brusselle GG,
Gharib SA,
Dupuis J,
Manichaikul A,
London SJ
Nature communications · 2018 · PMID 30061609 · open access
12 pages+
Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations
Sakornsakolpat P,
Prokopenko D,
Lamontagne M,
Reeve NF,
Guyatt AL,
Jackson VE,
Shrine N,
Qiao D,
Bartz TM,
Kim DK,
Lee MK,
Latourelle JC
and 42 more — show all
Li X,
Morrow JD,
Obeidat M,
Wyss AB,
Bakke P,
Barr RG,
Beaty TH,
Belinsky SA,
Brusselle GG,
Crapo JD,
de Jong K,
DeMeo DL,
Fingerlin TE,
Gharib SA,
Gulsvik A,
Hall IP,
Hokanson JE,
Kim WJ,
Lomas DA,
London SJ,
Meyers DA,
O'Connor GT,
Rennard SI,
Schwartz DA,
Sliwinski P,
Sparrow D,
Strachan DP,
Tal-Singer R,
Tesfaigzi Y,
Vestbo J,
Vonk JM,
Yim JJ,
Zhou X,
Bossé Y,
Manichaikul A,
Lahousse L,
Silverman EK,
Boezen HM,
Wain LV,
Tobin MD,
Hobbs BD,
Cho MH
SpiroMeta Consortium · International COPD Genetics Consortium
Nature genetics · 2019 · PMID 30804561 · open access
12 pages+
Insights into the genetic architecture of the human face
White JD,
Indencleef K,
Naqvi S,
Eller RJ,
Hoskens H,
Roosenboom J,
Lee MK,
Li J,
Mohammed J,
Richmond S,
Quillen EE,
Norton HL
and 11 more — show all
Feingold E,
Swigut T,
Marazita ML,
Peeters H,
Hens G,
Shaffer JR,
Wysocka J,
Walsh S,
Weinberg SM,
Shriver MD,
Claes P
Nature genetics · 2021 · PMID 33288918 · open access
12 pages+
Novel genetic loci affecting facial shape variation in humans
Xiong Z,
Dankova G,
Howe LJ,
Lee MK,
Hysi PG,
de Jong MA,
Zhu G,
Adhikari K,
Li D,
Li Y,
Pan B,
Feingold E
and 37 more — show all
Marazita ML,
Shaffer JR,
McAloney K,
Xu SH,
Jin L,
Wang S,
de Vrij FM,
Lendemeijer B,
Richmond S,
Zhurov A,
Lewis S,
Sharp GC,
Paternoster L,
Thompson H,
Gonzalez-Jose R,
Bortolini MC,
Canizales-Quinteros S,
Gallo C,
Poletti G,
Bedoya G,
Rothhammer F,
Uitterlinden AG,
Ikram MA,
Wolvius E,
Kushner SA,
Nijsten TE,
Palstra RT,
Boehringer S,
Medland SE,
Tang K,
Ruiz-Linares A,
Martin NG,
Spector TD,
Stergiakouli E,
Weinberg SM,
Liu F,
Kayser M
International Visible Trait Genetics (VisiGen) Consortium
eLife · 2019 · PMID 31763980 · open access
5 pages
Genome-wide association analysis identifies six new loci associated with forced vital capacity
Loth DW,
Soler Artigas M,
Gharib SA,
Wain LV,
Franceschini N,
Koch B,
Pottinger TD,
Smith AV,
Duan Q,
Oldmeadow C,
Lee MK,
Strachan DP
and 148 more — show all
James AL,
Huffman JE,
Vitart V,
Ramasamy A,
Wareham NJ,
Kaprio J,
Wang XQ,
Trochet H,
Kähönen M,
Flexeder C,
Albrecht E,
Lopez LM,
de Jong K,
Thyagarajan B,
Alves AC,
Enroth S,
Omenaas E,
Joshi PK,
Fall T,
Viñuela A,
Launer LJ,
Loehr LR,
Fornage M,
Li G,
Wilk JB,
Tang W,
Manichaikul A,
Lahousse L,
Harris TB,
North KE,
Rudnicka AR,
Hui J,
Gu X,
Lumley T,
Wright AF,
Hastie ND,
Campbell S,
Kumar R,
Pin I,
Scott RA,
Pietiläinen KH,
Surakka I,
Liu Y,
Holliday EG,
Schulz H,
Heinrich J,
Davies G,
Vonk JM,
Wojczynski M,
Pouta A,
Johansson A,
Wild SH,
Ingelsson E,
Rivadeneira F,
Völzke H,
Hysi PG,
Eiriksdottir G,
Morrison AC,
Rotter JI,
Gao W,
Postma DS,
White WB,
Rich SS,
Hofman A,
Aspelund T,
Couper D,
Smith LJ,
Psaty BM,
Lohman K,
Burchard EG,
Uitterlinden AG,
Garcia M,
Joubert BR,
McArdle WL,
Musk AB,
Hansel N,
Heckbert SR,
Zgaga L,
van Meurs JB,
Navarro P,
Rudan I,
Oh YM,
Redline S,
Jarvis DL,
Zhao JH,
Rantanen T,
O'Connor GT,
Ripatti S,
Scott RJ,
Karrasch S,
Grallert H,
Gaddis NC,
Starr JM,
Wijmenga C,
Minster RL,
Lederer DJ,
Pekkanen J,
Gyllensten U,
Campbell H,
Morris AP,
Gläser S,
Hammond CJ,
Burkart KM,
Beilby J,
Kritchevsky SB,
Gudnason V,
Hancock DB,
Williams OD,
Polasek O,
Zemunik T,
Kolcic I,
Petrini MF,
Wjst M,
Kim WJ,
Porteous DJ,
Scotland G,
Smith BH,
Viljanen A,
Heliövaara M,
Attia JR,
Sayers I,
Hampel R,
Gieger C,
Deary IJ,
Boezen HM,
Newman A,
Jarvelin MR,
Wilson JF,
Lind L,
Stricker BH,
Teumer A,
Spector TD,
Melén E,
Peters MJ,
Lange LA,
Barr RG,
Bracke KR,
Verhamme FM,
Sung J,
Hiemstra PS,
Cassano PA,
Sood A,
Hayward C,
Dupuis J,
Hall IP,
Brusselle GG,
Tobin MD,
London SJ
Nature genetics · 2014 · PMID 24929828
4 pages
Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape
Goovaerts S,
Hoskens H,
Eller RJ,
Herrick N,
Musolf AM,
Justice CM,
Yuan M,
Naqvi S,
Lee MK,
Vandermeulen D,
Szabo-Rogers HL,
Romitti PA
and 8 more — show all
Nature communications · 2023 · PMID 37973980 · open access
4 pages
Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology
Shaffer JR,
Orlova E,
Lee MK,
Leslie EJ,
Raffensperger ZD,
Heike CL,
Cunningham ML,
Hecht JT,
Kau CH,
Nidey NL,
Moreno LM,
Wehby GL
and 14 more — show all
Murray JC,
Laurie CA,
Laurie CC,
Cole J,
Ferrara T,
Ferrara T,
Santorico S,
Klein O,
Mio W,
Feingold E,
Hallgrimsson B,
Spritz RA,
Marazita ML,
Weinberg SM
PLoS genetics · 2016 · PMID 27560520 · open access
3 pages
Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis
Hobbs BD,
de Jong K,
Lamontagne M,
Bossé Y,
Shrine N,
Artigas MS,
Wain LV,
Hall IP,
Jackson VE,
Wyss AB,
London SJ,
North KE
and 64 more — show all
Franceschini N,
Strachan DP,
Beaty TH,
Hokanson JE,
Crapo JD,
Castaldi PJ,
Chase RP,
Bartz TM,
Heckbert SR,
Psaty BM,
Gharib SA,
Zanen P,
Lammers JW,
Oudkerk M,
Groen HJ,
Locantore N,
Tal-Singer R,
Rennard SI,
Vestbo J,
Timens W,
Paré PD,
Latourelle JC,
Dupuis J,
O'Connor GT,
Wilk JB,
Kim WJ,
Lee MK,
Oh YM,
Vonk JM,
de Koning HJ,
Leng S,
Belinsky SA,
Tesfaigzi Y,
Manichaikul A,
Wang XQ,
Rich SS,
Barr RG,
Sparrow D,
Litonjua AA,
Bakke P,
Gulsvik A,
Lahousse L,
Brusselle GG,
Stricker BH,
Uitterlinden AG,
Ampleford EJ,
Bleecker ER,
Woodruff PG,
Meyers DA,
Qiao D,
Lomas DA,
Yim JJ,
Kim DK,
Hawrylkiewicz I,
Sliwinski P,
Hardin M,
Fingerlin TE,
Schwartz DA,
Postma DS,
MacNee W,
Tobin MD,
Silverman EK,
Boezen HM,
Cho MH
COPDGene Investigators · ECLIPSE Investigators and 5 more consortia
Nature genetics · 2017 · PMID 28166215
3 pages
Investigating the shared genetics of non-syndromic cleft lip/palate and facial morphology
Howe LJ,
Lee MK,
Sharp GC,
Davey Smith G,
St Pourcain B,
Shaffer JR,
Ludwig KU,
Mangold E,
Marazita ML,
Feingold E,
Zhurov A,
Stergiakouli E
and 5 more — show all
PLoS genetics · 2018 · PMID 30067744 · open access
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.