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2,660 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.
4 matches for
O'Connell KS.
Genome-wide Association Analysis of Parkinson's Disease and Schizophrenia Reveals Shared Genetic Architecture and Identifies Novel Risk Loci
Smeland OB,
Shadrin A,
Bahrami S,
Broce I,
Tesli M,
Frei O,
Wirgenes KV,
O'Connell KS,
Krull F,
Bettella F,
Steen NE,
Sugrue L
and 10 more — show all
Biological psychiatry · 2021 · PMID 32201043
12 pages+
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
Mullins N,
Forstner AJ,
O'Connell KS,
Coombes B,
Coleman JRI,
Qiao Z,
Als TD,
Bigdeli TB,
Børte S,
Bryois J,
Charney AW,
Drange OK
and 305 more — show all
Gandal MJ,
Hagenaars SP,
Ikeda M,
Kamitaki N,
Kim M,
Krebs K,
Panagiotaropoulou G,
Schilder BM,
Sloofman LG,
Steinberg S,
Trubetskoy V,
Winsvold BS,
Won HH,
Abramova L,
Adorjan K,
Agerbo E,
Al Eissa M,
Albani D,
Alliey-Rodriguez N,
Anjorin A,
Antilla V,
Antoniou A,
Awasthi S,
Baek JH,
Bækvad-Hansen M,
Bass N,
Bauer M,
Beins EC,
Bergen SE,
Birner A,
Bøcker Pedersen C,
Bøen E,
Boks MP,
Bosch R,
Brum M,
Brumpton BM,
Brunkhorst-Kanaan N,
Budde M,
Bybjerg-Grauholm J,
Byerley W,
Cairns M,
Casas M,
Cervantes P,
Clarke TK,
Cruceanu C,
Cuellar-Barboza A,
Cunningham J,
Curtis D,
Czerski PM,
Dale AM,
Dalkner N,
David FS,
Degenhardt F,
Djurovic S,
Dobbyn AL,
Douzenis A,
Elvsåshagen T,
Escott-Price V,
Ferrier IN,
Fiorentino A,
Foroud TM,
Forty L,
Frank J,
Frei O,
Freimer NB,
Frisén L,
Gade K,
Garnham J,
Gelernter J,
Giørtz Pedersen M,
Gizer IR,
Gordon SD,
Gordon-Smith K,
Greenwood TA,
Grove J,
Guzman-Parra J,
Ha K,
Haraldsson M,
Hautzinger M,
Heilbronner U,
Hellgren D,
Herms S,
Hoffmann P,
Holmans PA,
Huckins L,
Jamain S,
Johnson JS,
Kalman JL,
Kamatani Y,
Kennedy JL,
Kittel-Schneider S,
Knowles JA,
Kogevinas M,
Koromina M,
Kranz TM,
Kranzler HR,
Kubo M,
Kupka R,
Kushner SA,
Lavebratt C,
Lawrence J,
Leber M,
Lee HJ,
Lee PH,
Levy SE,
Lewis C,
Liao C,
Lucae S,
Lundberg M,
MacIntyre DJ,
Magnusson SH,
Maier W,
Maihofer A,
Malaspina D,
Maratou E,
Martinsson L,
Mattheisen M,
McCarroll SA,
McGregor NW,
McGuffin P,
McKay JD,
Medeiros H,
Medland SE,
Millischer V,
Montgomery GW,
Moran JL,
Morris DW,
Mühleisen TW,
O'Brien N,
O'Donovan C,
Olde Loohuis LM,
Oruc L,
Papiol S,
Pardiñas AF,
Perry A,
Pfennig A,
Porichi E,
Potash JB,
Quested D,
Raj T,
Rapaport MH,
DePaulo JR,
Regeer EJ,
Rice JP,
Rivas F,
Rivera M,
Roth J,
Roussos P,
Ruderfer DM,
Sánchez-Mora C,
Schulte EC,
Senner F,
Sharp S,
Shilling PD,
Sigurdsson E,
Sirignano L,
Slaney C,
Smeland OB,
Smith DJ,
Sobell JL,
Søholm Hansen C,
Soler Artigas M,
Spijker AT,
Stein DJ,
Strauss JS,
Świątkowska B,
Terao C,
Thorgeirsson TE,
Toma C,
Tooney P,
Tsermpini EE,
Vawter MP,
Vedder H,
Walters JTR,
Witt SH,
Xi S,
Xu W,
Yang JMK,
Young AH,
Young H,
Zandi PP,
Zhou H,
Zillich L,
Adolfsson R,
Agartz I,
Alda M,
Alfredsson L,
Babadjanova G,
Backlund L,
Baune BT,
Bellivier F,
Bengesser S,
Berrettini WH,
Blackwood DHR,
Boehnke M,
Børglum AD,
Breen G,
Carr VJ,
Catts S,
Corvin A,
Craddock N,
Dannlowski U,
Dikeos D,
Esko T,
Etain B,
Ferentinos P,
Frye M,
Fullerton JM,
Gawlik M,
Gershon ES,
Goes FS,
Green MJ,
Grigoroiu-Serbanescu M,
Hauser J,
Henskens F,
Hillert J,
Hong KS,
Hougaard DM,
Hultman CM,
Hveem K,
Iwata N,
Jablensky AV,
Jones I,
Jones LA,
Kahn RS,
Kelsoe JR,
Kirov G,
Landén M,
Leboyer M,
Lewis CM,
Li QS,
Lissowska J,
Lochner C,
Loughland C,
Martin NG,
Mathews CA,
Mayoral F,
McElroy SL,
McIntosh AM,
McMahon FJ,
Melle I,
Michie P,
Milani L,
Mitchell PB,
Morken G,
Mors O,
Mortensen PB,
Mowry B,
Müller-Myhsok B,
Myers RM,
Neale BM,
Nievergelt CM,
Nordentoft M,
Nöthen MM,
O'Donovan MC,
Oedegaard KJ,
Olsson T,
Owen MJ,
Paciga SA,
Pantelis C,
Pato C,
Pato MT,
Patrinos GP,
Perlis RH,
Posthuma D,
Ramos-Quiroga JA,
Reif A,
Reininghaus EZ,
Ribasés M,
Rietschel M,
Ripke S,
Rouleau GA,
Saito T,
Schall U,
Schalling M,
Schofield PR,
Schulze TG,
Scott LJ,
Scott RJ,
Serretti A,
Shannon Weickert C,
Smoller JW,
Stefansson H,
Stefansson K,
Stordal E,
Streit F,
Sullivan PF,
Turecki G,
Vaaler AE,
Vieta E,
Vincent JB,
Waldman ID,
Weickert TW,
Werge T,
Wray NR,
Zwart JA,
Biernacka JM,
Nurnberger JI,
Cichon S,
Edenberg HJ,
Stahl EA,
McQuillin A,
Di Florio A,
Ophoff RA,
Andreassen OA
HUNT All-In Psychiatry
Nature genetics · 2021 · PMID 34002096 · open access
12 pages+
The genetic landscape of basal ganglia and implications for common brain disorders
Bahrami S,
Nordengen K,
Rokicki J,
Shadrin AA,
Rahman Z,
Smeland OB,
Jaholkowski PP,
Parker N,
Parekh P,
O'Connell KS,
Elvsåshagen T,
Toft M
and 5 more — show all
Nature communications · 2024 · PMID 39353893 · open access
7 pages
Genome-wide association study identifies 48 common genetic variants associated with handedness
Cuellar-Partida G,
Tung JY,
Eriksson N,
Albrecht E,
Aliev F,
Andreassen OA,
Barroso I,
Beckmann JS,
Boks MP,
Boomsma DI,
Boyd HA,
Breteler MMB
and 106 more — show all
Campbell H,
Chasman DI,
Cherkas LF,
Davies G,
de Geus EJC,
Deary IJ,
Deloukas P,
Dick DM,
Duffy DL,
Eriksson JG,
Esko T,
Feenstra B,
Geller F,
Gieger C,
Giegling I,
Gordon SD,
Han J,
Hansen TF,
Hartmann AM,
Hayward C,
Heikkilä K,
Hicks AA,
Hirschhorn JN,
Hottenga JJ,
Huffman JE,
Hwang LD,
Ikram MA,
Kaprio J,
Kemp JP,
Khaw KT,
Klopp N,
Konte B,
Kutalik Z,
Lahti J,
Li X,
Loos RJF,
Luciano M,
Magnusson SH,
Mangino M,
Marques-Vidal P,
Martin NG,
McArdle WL,
McCarthy MI,
Medina-Gomez C,
Melbye M,
Melville SA,
Metspalu A,
Milani L,
Mooser V,
Nelis M,
Nyholt DR,
O'Connell KS,
Ophoff RA,
Palmer C,
Palotie A,
Palviainen T,
Pare G,
Paternoster L,
Peltonen L,
Penninx BWJH,
Polasek O,
Pramstaller PP,
Prokopenko I,
Raikkonen K,
Ripatti S,
Rivadeneira F,
Rudan I,
Rujescu D,
Smit JH,
Smith GD,
Smoller JW,
Soranzo N,
Spector TD,
Pourcain BS,
Starr JM,
Stefánsson H,
Steinberg S,
Teder-Laving M,
Thorleifsson G,
Stefánsson K,
Timpson NJ,
Uitterlinden AG,
van Duijn CM,
van Rooij FJA,
Vink JM,
Vollenweider P,
Vuoksimaa E,
Waeber G,
Wareham NJ,
Warrington N,
Waterworth D,
Werge T,
Wichmann HE,
Widen E,
Willemsen G,
Wright AF,
Wright MJ,
Xu M,
Zhao JH,
Kraft P,
Hinds DA,
Lindgren CM,
Mägi R,
Neale BM,
Evans DM,
Medland SE
Nature human behaviour · 2021 · PMID 32989287
6 pages
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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.