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Squassina A.
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
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Yang Q,
de Rojas I,
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Chapuis J,
Ahmad S,
Giedraitis V,
Aarsland D,
Garcia-Gonzalez P,
Abdelnour C,
Alarcón-Martín E,
Alcolea D,
Alegret M,
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Armstrong NJ,
Tsolaki A,
Antúnez C,
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Arcaro M,
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Bailly H,
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Beiser A,
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Below JE,
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Grunin M,
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Guetta-Baranes T,
Haapasalo A,
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Haines JL,
Hamilton-Nelson KL,
Hampel H,
Hanon O,
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Hartmann AM,
Hausner L,
Harwood J,
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Helisalmi S,
Heneka MT,
Hernández I,
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Hoffmann P,
Holmes C,
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Jian X,
Johansson C,
Jun GR,
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Lage C,
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Lee CY,
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de Munain AL,
Love S,
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Ulstein I,
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Broeckhoven CV,
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van der Lugt A,
Dongen JV,
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Vandenberghe R,
Verhey F,
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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
Association of Polygenic Score for Schizophrenia and HLA Antigen and Inflammation Genes With Response to Lithium in Bipolar Affective Disorder: A Genome-Wide Association Study
Amare AT,
Schubert KO,
Hou L,
Clark SR,
Papiol S,
Heilbronner U,
Degenhardt F,
Tekola-Ayele F,
Hsu YH,
Shekhtman T,
Adli M,
Akula N
and 100 more — show all
Akiyama K,
Ardau R,
Arias B,
Aubry JM,
Backlund L,
Bhattacharjee AK,
Bellivier F,
Benabarre A,
Bengesser S,
Biernacka JM,
Birner A,
Brichant-Petitjean C,
Cervantes P,
Chen HC,
Chillotti C,
Cichon S,
Cruceanu C,
Czerski PM,
Dalkner N,
Dayer A,
Del Zompo M,
DePaulo JR,
Étain B,
Falkai P,
Forstner AJ,
Frisen L,
Frye MA,
Fullerton JM,
Gard S,
Garnham JS,
Goes FS,
Grigoroiu-Serbanescu M,
Grof P,
Hashimoto R,
Hauser J,
Herms S,
Hoffmann P,
Hofmann A,
Jamain S,
Jiménez E,
Kahn JP,
Kassem L,
Kuo PH,
Kato T,
Kelsoe J,
Kittel-Schneider S,
Kliwicki S,
König B,
Kusumi I,
Laje G,
Landén M,
Lavebratt C,
Leboyer M,
Leckband SG,
Tortorella A,
Manchia M,
Martinsson L,
McCarthy MJ,
McElroy S,
Colom F,
Mitjans M,
Mondimore FM,
Monteleone P,
Nievergelt CM,
Nöthen MM,
Novák T,
O'Donovan C,
Ozaki N,
Ösby U,
Pfennig A,
Potash JB,
Reif A,
Reininghaus E,
Rouleau GA,
Rybakowski JK,
Schalling M,
Schofield PR,
Schweizer BW,
Severino G,
Shilling PD,
Shimoda K,
Simhandl C,
Slaney CM,
Squassina A,
Stamm T,
Stopkova P,
Maj M,
Turecki G,
Vieta E,
Volkert J,
Witt S,
Wright A,
Zandi PP,
Mitchell PB,
Bauer M,
Alda M,
Rietschel M,
McMahon FJ,
Schulze TG,
Baune BT
International Consortium on Lithium Genetics (ConLi+Gen)
JAMA psychiatry · 2018 · PMID 29121268
5 pages
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder
Hou L,
Bergen SE,
Akula N,
Song J,
Hultman CM,
Landén M,
Adli M,
Alda M,
Ardau R,
Arias B,
Aubry JM,
Backlund L
and 127 more — show all
Badner JA,
Barrett TB,
Bauer M,
Baune BT,
Bellivier F,
Benabarre A,
Bengesser S,
Berrettini WH,
Bhattacharjee AK,
Biernacka JM,
Birner A,
Bloss CS,
Brichant-Petitjean C,
Bui ET,
Byerley W,
Cervantes P,
Chillotti C,
Cichon S,
Colom F,
Coryell W,
Craig DW,
Cruceanu C,
Czerski PM,
Davis T,
Dayer A,
Degenhardt F,
Del Zompo M,
DePaulo JR,
Edenberg HJ,
Étain B,
Falkai P,
Foroud T,
Forstner AJ,
Frisén L,
Frye MA,
Fullerton JM,
Gard S,
Garnham JS,
Gershon ES,
Goes FS,
Greenwood TA,
Grigoroiu-Serbanescu M,
Hauser J,
Heilbronner U,
Heilmann-Heimbach S,
Herms S,
Hipolito M,
Hitturlingappa S,
Hoffmann P,
Hofmann A,
Jamain S,
Jiménez E,
Kahn JP,
Kassem L,
Kelsoe JR,
Kittel-Schneider S,
Kliwicki S,
Koller DL,
König B,
Lackner N,
Laje G,
Lang M,
Lavebratt C,
Lawson WB,
Leboyer M,
Leckband SG,
Liu C,
Maaser A,
Mahon PB,
Maier W,
Maj M,
Manchia M,
Martinsson L,
McCarthy MJ,
McElroy SL,
McInnis MG,
McKinney R,
Mitchell PB,
Mitjans M,
Mondimore FM,
Monteleone P,
Mühleisen TW,
Nievergelt CM,
Nöthen MM,
Novák T,
Nurnberger JI Jr,
Nwulia EA,
Ösby U,
Pfennig A,
Potash JB,
Propping P,
Reif A,
Reininghaus E,
Rice J,
Rietschel M,
Rouleau GA,
Rybakowski JK,
Schalling M,
Scheftner WA,
Schofield PR,
Schork NJ,
Schulze TG,
Schumacher J,
Schweizer BW,
Severino G,
Shekhtman T,
Shilling PD,
Simhandl C,
Slaney CM,
Smith EN,
Squassina A,
Stamm T,
Stopkova P,
Streit F,
Strohmaier J,
Szelinger S,
Tighe SK,
Tortorella A,
Turecki G,
Vieta E,
Volkert J,
Witt SH,
Wright A,
Zandi PP,
Zhang P,
Zollner S,
McMahon FJ
Human molecular genetics · 2016 · PMID 27329760
2 pages
Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study
Hou L,
Heilbronner U,
Degenhardt F,
Adli M,
Akiyama K,
Akula N,
Ardau R,
Arias B,
Backlund L,
Banzato CEM,
Benabarre A,
Bengesser S
and 111 more — show all
Bhattacharjee AK,
Biernacka JM,
Birner A,
Brichant-Petitjean C,
Bui ET,
Cervantes P,
Chen GB,
Chen HC,
Chillotti C,
Cichon S,
Clark SR,
Colom F,
Cousins DA,
Cruceanu C,
Czerski PM,
Dantas CR,
Dayer A,
Étain B,
Falkai P,
Forstner AJ,
Frisén L,
Fullerton JM,
Gard S,
Garnham JS,
Goes FS,
Grof P,
Gruber O,
Hashimoto R,
Hauser J,
Herms S,
Hoffmann P,
Hofmann A,
Jamain S,
Jiménez E,
Kahn JP,
Kassem L,
Kittel-Schneider S,
Kliwicki S,
König B,
Kusumi I,
Lackner N,
Laje G,
Landén M,
Lavebratt C,
Leboyer M,
Leckband SG,
Jaramillo CAL,
MacQueen G,
Manchia M,
Martinsson L,
Mattheisen M,
McCarthy MJ,
McElroy SL,
Mitjans M,
Mondimore FM,
Monteleone P,
Nievergelt CM,
Nöthen MM,
Ösby U,
Ozaki N,
Perlis RH,
Pfennig A,
Reich-Erkelenz D,
Rouleau GA,
Schofield PR,
Schubert KO,
Schweizer BW,
Seemüller F,
Severino G,
Shekhtman T,
Shilling PD,
Shimoda K,
Simhandl C,
Slaney CM,
Smoller JW,
Squassina A,
Stamm T,
Stopkova P,
Tighe SK,
Tortorella A,
Turecki G,
Volkert J,
Witt S,
Wright A,
Young LT,
Zandi PP,
Potash JB,
DePaulo JR,
Bauer M,
Reininghaus EZ,
Novák T,
Aubry JM,
Maj M,
Baune BT,
Mitchell PB,
Vieta E,
Frye MA,
Rybakowski JK,
Kuo PH,
Kato T,
Grigoroiu-Serbanescu M,
Reif A,
Del Zompo M,
Bellivier F,
Schalling M,
Wray NR,
Kelsoe JR,
Alda M,
Rietschel M,
McMahon FJ,
Schulze TG
Lancet (London, England) · 2016 · PMID 26806518 · open access
1 page
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
Sims R,
van der Lee SJ,
Naj AC,
Bellenguez C,
Badarinarayan N,
Jakobsdottir J,
Kunkle BW,
Boland A,
Raybould R,
Bis JC,
Martin ER,
Grenier-Boley B
and 437 more — show all
Heilmann-Heimbach S,
Chouraki V,
Kuzma AB,
Sleegers K,
Vronskaya M,
Ruiz A,
Graham RR,
Olaso R,
Hoffmann P,
Grove ML,
Vardarajan BN,
Hiltunen M,
Nöthen MM,
White CC,
Hamilton-Nelson KL,
Epelbaum J,
Maier W,
Choi SH,
Beecham GW,
Dulary C,
Herms S,
Smith AV,
Funk CC,
Derbois C,
Forstner AJ,
Ahmad S,
Li H,
Bacq D,
Harold D,
Satizabal CL,
Valladares O,
Squassina A,
Thomas R,
Brody JA,
Qu L,
Sánchez-Juan P,
Morgan T,
Wolters FJ,
Zhao Y,
Garcia FS,
Denning N,
Fornage M,
Malamon J,
Naranjo MCD,
Majounie E,
Mosley TH,
Dombroski B,
Wallon D,
Lupton MK,
Dupuis J,
Whitehead P,
Fratiglioni L,
Medway C,
Jian X,
Mukherjee S,
Keller L,
Brown K,
Lin H,
Cantwell LB,
Panza F,
McGuinness B,
Moreno-Grau S,
Burgess JD,
Solfrizzi V,
Proitsi P,
Adams HH,
Allen M,
Seripa D,
Pastor P,
Cupples LA,
Price ND,
Hannequin D,
Frank-García A,
Levy D,
Chakrabarty P,
Caffarra P,
Giegling I,
Beiser AS,
Giedraitis V,
Hampel H,
Garcia ME,
Wang X,
Lannfelt L,
Mecocci P,
Eiriksdottir G,
Crane PK,
Pasquier F,
Boccardi V,
Henández I,
Barber RC,
Scherer M,
Tarraga L,
Adams PM,
Leber M,
Chen Y,
Albert MS,
Riedel-Heller S,
Emilsson V,
Beekly D,
Braae A,
Schmidt R,
Blacker D,
Masullo C,
Schmidt H,
Doody RS,
Spalletta G,
Longstreth WT Jr,
Fairchild TJ,
Bossù P,
Lopez OL,
Frosch MP,
Sacchinelli E,
Ghetti B,
Yang Q,
Huebinger RM,
Jessen F,
Li S,
Kamboh MI,
Morris J,
Sotolongo-Grau O,
Katz MJ,
Corcoran C,
Dunstan M,
Braddel A,
Thomas C,
Meggy A,
Marshall R,
Gerrish A,
Chapman J,
Aguilar M,
Taylor S,
Hill M,
Fairén MD,
Hodges A,
Vellas B,
Soininen H,
Kloszewska I,
Daniilidou M,
Uphill J,
Patel Y,
Hughes JT,
Lord J,
Turton J,
Hartmann AM,
Cecchetti R,
Fenoglio C,
Serpente M,
Arcaro M,
Caltagirone C,
Orfei MD,
Ciaramella A,
Pichler S,
Mayhaus M,
Gu W,
Lleó A,
Fortea J,
Blesa R,
Barber IS,
Brookes K,
Cupidi C,
Maletta RG,
Carrell D,
Sorbi S,
Moebus S,
Urbano M,
Pilotto A,
Kornhuber J,
Bosco P,
Todd S,
Craig D,
Johnston J,
Gill M,
Lawlor B,
Lynch A,
Fox NC,
Hardy J,
Albin RL,
Apostolova LG,
Arnold SE,
Asthana S,
Atwood CS,
Baldwin CT,
Barnes LL,
Barral S,
Beach TG,
Becker JT,
Bigio EH,
Bird TD,
Boeve BF,
Bowen JD,
Boxer A,
Burke JR,
Burns JM,
Buxbaum JD,
Cairns NJ,
Cao C,
Carlson CS,
Carlsson CM,
Carney RM,
Carrasquillo MM,
Carroll SL,
Diaz CC,
Chui HC,
Clark DG,
Cribbs DH,
Crocco EA,
DeCarli C,
Dick M,
Duara R,
Evans DA,
Faber KM,
Fallon KB,
Fardo DW,
Farlow MR,
Ferris S,
Foroud TM,
Galasko DR,
Gearing M,
Geschwind DH,
Gilbert JR,
Graff-Radford NR,
Green RC,
Growdon JH,
Hamilton RL,
Harrell LE,
Honig LS,
Huentelman MJ,
Hulette CM,
Hyman BT,
Jarvik GP,
Abner E,
Jin LW,
Jun G,
Karydas A,
Kaye JA,
Kim R,
Kowall NW,
Kramer JH,
LaFerla FM,
Lah JJ,
Leverenz JB,
Levey AI,
Li G,
Lieberman AP,
Lunetta KL,
Lyketsos CG,
Marson DC,
Martiniuk F,
Mash DC,
Masliah E,
McCormick WC,
McCurry SM,
McDavid AN,
McKee AC,
Mesulam M,
Miller BL,
Miller CA,
Miller JW,
Morris JC,
Murrell JR,
Myers AJ,
O'Bryant S,
Olichney JM,
Pankratz VS,
Parisi JE,
Paulson HL,
Perry W,
Peskind E,
Pierce A,
Poon WW,
Potter H,
Quinn JF,
Raj A,
Raskind M,
Reisberg B,
Reitz C,
Ringman JM,
Roberson ED,
Rogaeva E,
Rosen HJ,
Rosenberg RN,
Sager MA,
Saykin AJ,
Schneider JA,
Schneider LS,
Seeley WW,
Smith AG,
Sonnen JA,
Spina S,
Stern RA,
Swerdlow RH,
Tanzi RE,
Thornton-Wells TA,
Trojanowski JQ,
Troncoso JC,
Van Deerlin VM,
Van Eldik LJ,
Vinters HV,
Vonsattel JP,
Weintraub S,
Welsh-Bohmer KA,
Wilhelmsen KC,
Williamson J,
Wingo TS,
Woltjer RL,
Wright CB,
Yu CE,
Yu L,
Garzia F,
Golamaully F,
Septier G,
Engelborghs S,
Vandenberghe R,
De Deyn PP,
Fernadez CM,
Benito YA,
Thonberg H,
Forsell C,
Lilius L,
Kinhult-Stählbom A,
Kilander L,
Brundin R,
Concari L,
Helisalmi S,
Koivisto AM,
Haapasalo A,
Dermecourt V,
Fievet N,
Hanon O,
Dufouil C,
Brice A,
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Aspelund T,
Larson EB,
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Rotter JI,
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Montine TJ,
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Boerwinkle E,
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Rivadeneira F,
Reiman EM,
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Bruni AC,
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Holmes C,
Cruchaga C,
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Bennett DA,
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Passmore P,
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Dickson DW,
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Escott-Price V,
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ARUK Consortium · GERAD/PERADES, CHARGE, ADGC, EADI
Nature genetics · 2017 · PMID 28714976
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