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10 matches for
Shadrin A.
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+
Vertex-wise multivariate genome-wide association study identifies 780 unique genetic loci associated with cortical morphology
Shadrin AA,
Kaufmann T,
van der Meer D,
Palmer CE,
Makowski C,
Loughnan R,
Jernigan TL,
Seibert TM,
Hagler DJ,
Smeland OB,
Motazedi E,
Chu Y
and 10 more — show all
NeuroImage · 2021 · PMID 34560273
12 pages+
The genetic architecture of human cortical folding
van der Meer D,
Kaufmann T,
Shadrin AA,
Makowski C,
Frei O,
Roelfs D,
Monereo-Sánchez J,
Linden DEJ,
Rokicki J,
Alnæs D,
de Leeuw C,
Thompson WK
and 5 more — show all
Science advances · 2021 · PMID 34910505 · open access
12 pages+
The genetic architecture of human cerebellar morphology supports a key role for the cerebellum in human evolution and psychopathology
Moberget T,
van der Meer D,
Bahrami S,
Roelfs D,
Frei O,
Kaufmann T,
Fernandez-Cabello S,
Kim M,
Wolfers T,
Diedrichsen J,
Smeland OB,
Shadrin A
and 3 more — show all
Communications biology · 2026 · PMID 41703085 · open access
12 pages+
The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition
van der Meer D,
Gurholt TP,
Sønderby IE,
Shadrin AA,
Hindley G,
Rahman Z,
de Lange AG,
Frei O,
Leinhard OD,
Linge J,
Simon R,
Beck D
and 6 more — show all
Communications biology · 2022 · PMID 36402844 · open access
10 pages
New insights into the genetic etiology of Alzheimer's disease and related dementias
Bellenguez C,
Küçükali F,
Jansen IE,
Kleineidam L,
Moreno-Grau S,
Amin N,
Naj AC,
Campos-Martin R,
Grenier-Boley B,
Andrade V,
Holmans PA,
Boland A
and 391 more — show all
Damotte V,
van der Lee SJ,
Costa MR,
Kuulasmaa T,
Yang Q,
de Rojas I,
Bis JC,
Yaqub A,
Prokic I,
Chapuis J,
Ahmad S,
Giedraitis V,
Aarsland D,
Garcia-Gonzalez P,
Abdelnour C,
Alarcón-Martín E,
Alcolea D,
Alegret M,
Alvarez I,
Álvarez V,
Armstrong NJ,
Tsolaki A,
Antúnez C,
Appollonio I,
Arcaro M,
Archetti S,
Pastor AA,
Arosio B,
Athanasiu L,
Bailly H,
Banaj N,
Baquero M,
Barral S,
Beiser A,
Pastor AB,
Below JE,
Benchek P,
Benussi L,
Berr C,
Besse C,
Bessi V,
Binetti G,
Bizarro A,
Blesa R,
Boada M,
Boerwinkle E,
Borroni B,
Boschi S,
Bossù P,
Bråthen G,
Bressler J,
Bresner C,
Brodaty H,
Brookes KJ,
Brusco LI,
Buiza-Rueda D,
Bûrger K,
Burholt V,
Bush WS,
Calero M,
Cantwell LB,
Chene G,
Chung J,
Cuccaro ML,
Carracedo Á,
Cecchetti R,
Cervera-Carles L,
Charbonnier C,
Chen HH,
Chillotti C,
Ciccone S,
Claassen JAHR,
Clark C,
Conti E,
Corma-Gómez A,
Costantini E,
Custodero C,
Daian D,
Dalmasso MC,
Daniele A,
Dardiotis E,
Dartigues JF,
de Deyn PP,
de Paiva Lopes K,
de Witte LD,
Debette S,
Deckert J,
Del Ser T,
Denning N,
DeStefano A,
Dichgans M,
Diehl-Schmid J,
Diez-Fairen M,
Rossi PD,
Djurovic S,
Duron E,
Düzel E,
Dufouil C,
Eiriksdottir G,
Engelborghs S,
Escott-Price V,
Espinosa A,
Ewers M,
Faber KM,
Fabrizio T,
Nielsen SF,
Fardo DW,
Farotti L,
Fenoglio C,
Fernández-Fuertes M,
Ferrari R,
Ferreira CB,
Ferri E,
Fin B,
Fischer P,
Fladby T,
Fließbach K,
Fongang B,
Fornage M,
Fortea J,
Foroud TM,
Fostinelli S,
Fox NC,
Franco-Macías E,
Bullido MJ,
Frank-García A,
Froelich L,
Fulton-Howard B,
Galimberti D,
García-Alberca JM,
García-González P,
Garcia-Madrona S,
Garcia-Ribas G,
Ghidoni R,
Giegling I,
Giorgio G,
Goate AM,
Goldhardt O,
Gomez-Fonseca D,
González-Pérez A,
Graff C,
Grande G,
Green E,
Grimmer T,
Grünblatt E,
Grunin M,
Gudnason V,
Guetta-Baranes T,
Haapasalo A,
Hadjigeorgiou G,
Haines JL,
Hamilton-Nelson KL,
Hampel H,
Hanon O,
Hardy J,
Hartmann AM,
Hausner L,
Harwood J,
Heilmann-Heimbach S,
Helisalmi S,
Heneka MT,
Hernández I,
Herrmann MJ,
Hoffmann P,
Holmes C,
Holstege H,
Vilas RH,
Hulsman M,
Humphrey J,
Biessels GJ,
Jian X,
Johansson C,
Jun GR,
Kastumata Y,
Kauwe J,
Kehoe PG,
Kilander L,
Ståhlbom AK,
Kivipelto M,
Koivisto A,
Kornhuber J,
Kosmidis MH,
Kukull WA,
Kuksa PP,
Kunkle BW,
Kuzma AB,
Lage C,
Laukka EJ,
Launer L,
Lauria A,
Lee CY,
Lehtisalo J,
Lerch O,
Lleó A,
Longstreth W Jr,
Lopez O,
de Munain AL,
Love S,
Löwemark M,
Luckcuck L,
Lunetta KL,
Ma Y,
Macías J,
MacLeod CA,
Maier W,
Mangialasche F,
Spallazzi M,
Marquié M,
Marshall R,
Martin ER,
Montes AM,
Rodríguez CM,
Masullo C,
Mayeux R,
Mead S,
Mecocci P,
Medina M,
Meggy A,
Mehrabian S,
Mendoza S,
Menéndez-González M,
Mir P,
Moebus S,
Mol M,
Molina-Porcel L,
Montrreal L,
Morelli L,
Moreno F,
Morgan K,
Mosley T,
Nöthen MM,
Muchnik C,
Mukherjee S,
Nacmias B,
Ngandu T,
Nicolas G,
Nordestgaard BG,
Olaso R,
Orellana A,
Orsini M,
Ortega G,
Padovani A,
Paolo C,
Papenberg G,
Parnetti L,
Pasquier F,
Pastor P,
Peloso G,
Pérez-Cordón A,
Pérez-Tur J,
Pericard P,
Peters O,
Pijnenburg YAL,
Pineda JA,
Piñol-Ripoll G,
Pisanu C,
Polak T,
Popp J,
Posthuma D,
Priller J,
Puerta R,
Quenez O,
Quintela I,
Thomassen JQ,
Rábano A,
Rainero I,
Rajabli F,
Ramakers I,
Real LM,
Reinders MJT,
Reitz C,
Reyes-Dumeyer D,
Ridge P,
Riedel-Heller S,
Riederer P,
Roberto N,
Rodriguez-Rodriguez E,
Rongve A,
Allende IR,
Rosende-Roca M,
Royo JL,
Rubino E,
Rujescu D,
Sáez ME,
Sakka P,
Saltvedt I,
Sanabria Á,
Sánchez-Arjona MB,
Sanchez-Garcia F,
Juan PS,
Sánchez-Valle R,
Sando SB,
Sarnowski C,
Satizabal CL,
Scamosci M,
Scarmeas N,
Scarpini E,
Scheltens P,
Scherbaum N,
Scherer M,
Schmid M,
Schneider A,
Schott JM,
Selbæk G,
Seripa D,
Serrano M,
Sha J,
Shadrin AA,
Skrobot O,
Slifer S,
Snijders GJL,
Soininen H,
Solfrizzi V,
Solomon A,
Song Y,
Sorbi S,
Sotolongo-Grau O,
Spalletta G,
Spottke A,
Squassina A,
Stordal E,
Tartan JP,
Tárraga L,
Tesí N,
Thalamuthu A,
Thomas T,
Tosto G,
Traykov L,
Tremolizzo L,
Tybjærg-Hansen A,
Uitterlinden A,
Ullgren A,
Ulstein I,
Valero S,
Valladares O,
Broeckhoven CV,
Vance J,
Vardarajan BN,
van der Lugt A,
Dongen JV,
van Rooij J,
van Swieten J,
Vandenberghe R,
Verhey F,
Vidal JS,
Vogelgsang J,
Vyhnalek M,
Wagner M,
Wallon D,
Wang LS,
Wang R,
Weinhold L,
Wiltfang J,
Windle G,
Woods B,
Yannakoulia M,
Zare H,
Zhao Y,
Zhang X,
Zhu C,
Zulaica M,
Farrer LA,
Psaty BM,
Ghanbari M,
Raj T,
Sachdev P,
Mather K,
Jessen F,
Ikram MA,
de Mendonça A,
Hort J,
Tsolaki M,
Pericak-Vance MA,
Amouyel P,
Williams J,
Frikke-Schmidt R,
Clarimon J,
Deleuze JF,
Rossi G,
Seshadri S,
Andreassen OA,
Ingelsson M,
Hiltunen M,
Sleegers K,
Schellenberg GD,
van Duijn CM,
Sims R,
van der Flier WM,
Ruiz A,
Ramirez A,
Lambert JC
EADB · GR@ACE and 7 more consortia
Nature genetics · 2022 · PMID 35379992 · open access
9 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
Large-scale brainstem neuroimaging and genetic analyses provide new insights into the neuronal mechanisms of hypertension
Gurholt TP,
Elvsåshagen T,
Bahrami S,
Rahman Z,
Shadrin A,
Askeland-Gjerde DE,
van der Meer D,
Frei O,
Kaufmann T,
Sønderby IE,
Halvorsen S,
Westlye LT
and 1 more — show all
HGG advances · 2025 · PMID 39663699 · open access
7 pages
Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers
Jansen IE,
van der Lee SJ,
Gomez-Fonseca D,
de Rojas I,
Dalmasso MC,
Grenier-Boley B,
Zettergren A,
Mishra A,
Ali M,
Andrade V,
Bellenguez C,
Kleineidam L
and 134 more — show all
Küçükali F,
Sung YJ,
Tesí N,
Vromen EM,
Wightman DP,
Alcolea D,
Alegret M,
Alvarez I,
Amouyel P,
Athanasiu L,
Bahrami S,
Bailly H,
Belbin O,
Bergh S,
Bertram L,
Biessels GJ,
Blennow K,
Blesa R,
Boada M,
Boland A,
Buerger K,
Carracedo Á,
Cervera-Carles L,
Chene G,
Claassen JAHR,
Debette S,
Deleuze JF,
de Deyn PP,
Diehl-Schmid J,
Djurovic S,
Dols-Icardo O,
Dufouil C,
Duron E,
Düzel E,
Fladby T,
Fortea J,
Frölich L,
García-González P,
Garcia-Martinez M,
Giegling I,
Goldhardt O,
Gobom J,
Grimmer T,
Haapasalo A,
Hampel H,
Hanon O,
Hausner L,
Heilmann-Heimbach S,
Helisalmi S,
Heneka MT,
Hernández I,
Herukka SK,
Holstege H,
Jarholm J,
Kern S,
Knapskog AB,
Koivisto AM,
Kornhuber J,
Kuulasmaa T,
Lage C,
Laske C,
Leinonen V,
Lewczuk P,
Lleó A,
de Munain AL,
Lopez-Garcia S,
Maier W,
Marquié M,
Mol MO,
Montrreal L,
Moreno F,
Moreno-Grau S,
Nicolas G,
Nöthen MM,
Orellana A,
Pålhaugen L,
Papma JM,
Pasquier F,
Perneczky R,
Peters O,
Pijnenburg YAL,
Popp J,
Posthuma D,
Pozueta A,
Priller J,
Puerta R,
Quintela I,
Ramakers I,
Rodriguez-Rodriguez E,
Rujescu D,
Saltvedt I,
Sanchez-Juan P,
Scheltens P,
Scherbaum N,
Schmid M,
Schneider A,
Selbæk G,
Selnes P,
Shadrin A,
Skoog I,
Soininen H,
Tárraga L,
Teipel S,
Tijms B,
Tsolaki M,
Van Broeckhoven C,
Van Dongen J,
van Swieten JC,
Vandenberghe R,
Vidal JS,
Visser PJ,
Vogelgsang J,
Waern M,
Wagner M,
Wiltfang J,
Wittens MMJ,
Zetterberg H,
Zulaica M,
van Duijn CM,
Bjerke M,
Engelborghs S,
Jessen F,
Teunissen CE,
Pastor P,
Hiltunen M,
Ingelsson M,
Andreassen OA,
Clarimón J,
Sleegers K,
Ruiz A,
Ramirez A,
Cruchaga C,
Lambert JC,
van der Flier W
EADB consortium · GR@ACE study group
Acta neuropathologica · 2022 · PMID 36066633 · open access
3 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
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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.
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It is rebuilt from the pages every hour. A paper appears the moment a page starts
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