The current state of genetic risk models for the development of kidney cancer: a review and validation.
Bju International
Harrison, Hannah H; Li, Nicole N; Saunders, Catherine L CL; Rossi, Sabrina H SH; Dennis, Joe J; Griffin, Simon J SJ; Stewart, Grant D GD; Usher-Smith, Juliet A JA
Genome-wide analysis identifies a novel LINC-PINT splice variant associated with vascular amyloid pathology in Alzheimer's disease.
Acta Neuropathologica Communications
Reddy, Joseph S JS; Allen, Mariet M; Ho, Charlotte C G CCG; Oatman, Stephanie R SR; İş, Özkan Ö; Quicksall, Zachary S ZS; Wang, Xue X; Jin, Jiangli J; Patel, Tulsi A TA; Carnwath, Troy P TP; Nguyen, Thuy T TT; Malphrus, Kimberly G KG; Lincoln, Sarah J SJ; Carrasquillo, Minerva M MM; Crook, Julia E JE; Kanekiyo, Takahisa T; Murray, Melissa E ME; Bu, Guojun G; Dickson, Dennis W DW; Ertekin-Taner, Nilüfer N
A telescope GWAS analysis strategy, based on SNPs-genes-pathways ensamble and on multivariate algorithms, to characterize late onset Alzheimer's disease.
Shared mechanisms for cognitive impairment and physical frailty: A model for complex systems.
Alzheimer'S & Dementia (New York, N. Y.)
Sargent, Lana L; Nalls, Mike M; Amella, Elaine J EJ; Slattum, Patricia W PW; Mueller, Martina M; Bandinelli, Stefania S; Tian, Qu Q; Swift-Scanlan, Theresa T; Lageman, Sarah K SK; Singleton, Andrew A
Genetic analysis of hsCRP in American Indians: The Strong Heart Family Study.
Plos One
Best, Lyle G LG; Balakrishnan, Poojitha P; Cole, Shelley A SA; Haack, Karin K; Kocarnik, Jonathan M JM; Pankratz, Nathan N; Anderson, Matthew Z MZ; Franceschini, Nora N; Howard, Barbara V BV; Lee, Elisa T ET; North, Kari E KE; Umans, Jason G JG; Yracheta, Joseph M JM; Navas-Acien, Ana A; Voruganti, V Saroja VS
Non-coding variability at the APOE locus contributes to the Alzheimer's risk.
Nature Communications
Zhou, Xiaopu X; Chen, Yu Y; Mok, Kin Y KY; Kwok, Timothy C Y TCY; Mok, Vincent C T VCT; Guo, Qihao Q; Ip, Fanny C FC; Chen, Yuewen Y; Mullapudi, Nandita N; , ; Giusti-Rodríguez, Paola P; Sullivan, Patrick F PF; Hardy, John J; Fu, Amy K Y AKY; Li, Yun Y; Ip, Nancy Y NY
A candidate gene study of risk for dementia in older, postmenopausal women: Results from the Women's Health Initiative Memory Study.
International Journal Of Geriatric Psychiatry
Driscoll, Ira I; Snively, Beverly M BM; Espeland, Mark A MA; Shumaker, Sally A SA; Rapp, Stephen R SR; Goveas, Joseph S JS; Casanova, Ramon L RL; Wactawski-Wende, Jean J; Manson, JoAnn E JE; Rossom, Rebecca R; Brooks, Janet J; Hernandez, Dena G DG; Singleton, Andrew B AB; Resnick, Susan M SM
Biothiols and oxidative stress markers and polymorphisms of TOMM40 and APOC1 genes in Alzheimer's disease patients.
Oncotarget
Prendecki, Michal M; Florczak-Wyspianska, Jolanta J; Kowalska, Marta M; Ilkowski, Jan J; Grzelak, Teresa T; Bialas, Katarzyna K; Wiszniewska, Malgorzata M; Kozubski, Wojciech W; Dorszewska, Jolanta J
Population-Wide Genetic Risk Prediction of Complex Diseases: A Pilot Feasibility Study in Macau Population for Precision Public Healthcare Planning.
Scientific Reports
Tsui, Nancy B Y NBY; Cheng, Gregory G; Chung, Teresa T; Lam, Christopher W K CWK; Yee, Anita A; Chung, Peter K C PKC; Kwan, Tsz-Ki TK; Ko, Elaine E; He, Daihai D; Wong, Wing-Tak WT; Lau, Johnson Y N JYN; Lau, Lok Ting LT; Fok, Manson M
Hidden heterogeneity in Alzheimer's disease: Insights from genetic association studies and other analyses.
Experimental Gerontology
Yashin, Anatoliy I AI; Fang, Fang F; Kovtun, Mikhail M; Wu, Deqing D; Duan, Matt M; Arbeev, Konstantin K; Akushevich, Igor I; Kulminski, Alexander A; Culminskaya, Irina I; Zhbannikov, Ilya I; Yashkin, Arseniy A; Stallard, Eric E; Ukraintseva, Svetlana S
A novel SCCA approach via truncated ℓ1-norm and truncated group lasso for brain imaging genetics.
Bioinformatics (Oxford, England)
Du, Lei L; Liu, Kefei K; Zhang, Tuo T; Yao, Xiaohui X; Yan, Jingwen J; Risacher, Shannon L SL; Han, Junwei J; Guo, Lei L; Saykin, Andrew J AJ; Shen, Li L; ,
Genome-wide association interaction analysis for Alzheimer's disease.
Neurobiology Of Aging
Gusareva, Elena S ES; Carrasquillo, Minerva M MM; Bellenguez, Céline C; Cuyvers, Elise E; Colon, Samuel S; Graff-Radford, Neill R NR; Petersen, Ronald C RC; Dickson, Dennis W DW; Mahachie John, Jestinah M JM; Bessonov, Kyrylo K; Van Broeckhoven, Christine C; , ; Harold, Denise D; Williams, Julie J; Amouyel, Philippe P; Sleegers, Kristel K; Ertekin-Taner, Nilüfer N; Lambert, Jean-Charles JC; Van Steen, Kristel K
Overrepresentation of glutamate signaling in Alzheimer's disease: network-based pathway enrichment using meta-analysis of genome-wide association studies.
Plos One
Pérez-Palma, Eduardo E; Bustos, Bernabé I BI; Villamán, Camilo F CF; Alarcón, Marcelo A MA; Avila, Miguel E ME; Ugarte, Giorgia D GD; Reyes, Ariel E AE; Opazo, Carlos C; De Ferrari, Giancarlo V GV; , ; ,
Genetic loci associated with Alzheimer's disease and cerebrospinal fluid biomarkers in a Finnish case-control cohort.
Plos One
Elias-Sonnenschein, Lyzel S LS; Helisalmi, Seppo S; Natunen, Teemu T; Hall, Anette A; Paajanen, Teemu T; Herukka, Sanna-Kaisa SK; Laitinen, Marjo M; Remes, Anne M AM; Koivisto, Anne M AM; Mattila, Kari M KM; Lehtimäki, Terho T; Verhey, Frans R J FR; Visser, Pieter Jelle PJ; Soininen, Hilkka H; Hiltunen, Mikko M
Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained.
Plos Genetics
Wu, Ying Y; Waite, Lindsay L LL; Jackson, Anne U AU; Sheu, Wayne H-H WH; Buyske, Steven S; Absher, Devin D; Arnett, Donna K DK; Boerwinkle, Eric E; Bonnycastle, Lori L LL; Carty, Cara L CL; Cheng, Iona I; Cochran, Barbara B; Croteau-Chonka, Damien C DC; Dumitrescu, Logan L; Eaton, Charles B CB; Franceschini, Nora N; Guo, Xiuqing X; Henderson, Brian E BE; Hindorff, Lucia A LA; Kim, Eric E; Kinnunen, Leena L; Komulainen, Pirjo P; Lee, Wen-Jane WJ; Le Marchand, Loic L; Lin, Yi Y; Lindström, Jaana J; Lingaas-Holmen, Oddgeir O; Mitchell, Sabrina L SL; Narisu, Narisu N; Robinson, Jennifer G JG; Schumacher, Fred F; Stančáková, Alena A; Sundvall, Jouko J; Sung, Yun-Ju YJ; Swift, Amy J AJ; Wang, Wen-Chang WC; Wilkens, Lynne L; Wilsgaard, Tom T; Young, Alicia M AM; Adair, Linda S LS; Ballantyne, Christie M CM; Bůžková, Petra P; Chakravarti, Aravinda A; Collins, Francis S FS; Duggan, David D; Feranil, Alan B AB; Ho, Low-Tone LT; Hung, Yi-Jen YJ; Hunt, Steven C SC; Hveem, Kristian K; Juang, Jyh-Ming J JM; Kesäniemi, Antero Y AY; Kuusisto, Johanna J; Laakso, Markku M; Lakka, Timo A TA; Lee, I-Te IT; Leppert, Mark F MF; Matise, Tara C TC; Moilanen, Leena L; Njølstad, Inger I; Peters, Ulrike U; Quertermous, Thomas T; Rauramaa, Rainer R; Rotter, Jerome I JI; Saramies, Jouko J; Tuomilehto, Jaakko J; Uusitupa, Matti M; Wang, Tzung-Dau TD; Boehnke, Michael M; Haiman, Christopher A CA; Chen, Yii-Der I YD; Kooperberg, Charles C; Assimes, Themistocles L TL; Crawford, Dana C DC; Hsiung, Chao A CA; North, Kari E KE; Mohlke, Karen L KL
Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis.
Human Molecular Genetics
Lee, S Hong SH; Harold, Denise D; Nyholt, Dale R DR; , ; , ; , ; Goddard, Michael E ME; Zondervan, Krina T KT; Williams, Julie J; Montgomery, Grant W GW; Wray, Naomi R NR; Visscher, Peter M PM
Comprehensive search for Alzheimer disease susceptibility loci in the APOE region.
Archives Of Neurology
Jun, Gyungah G; Vardarajan, Badri N BN; Buros, Jacqueline J; Yu, Chang-En CE; Hawk, Michele V MV; Dombroski, Beth A BA; Crane, Paul K PK; Larson, Eric B EB; , ; Mayeux, Richard R; Haines, Jonathan L JL; Lunetta, Kathryn L KL; Pericak-Vance, Margaret A MA; Schellenberg, Gerard D GD; Farrer, Lindsay A LA
Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe project.
Plos One
Musunuru, Kiran K; Romaine, Simon P R SP; Lettre, Guillaume G; Wilson, James G JG; Volcik, Kelly A KA; Tsai, Michael Y MY; Taylor, Herman A HA; Schreiner, Pamela J PJ; Rotter, Jerome I JI; Rich, Stephen S SS; Redline, Susan S; Psaty, Bruce M BM; Papanicolaou, George J GJ; Ordovas, Jose M JM; Liu, Kiang K; Krauss, Ronald M RM; Glazer, Nicole L NL; Gabriel, Stacey B SB; Fornage, Myriam M; Cupples, L Adrienne LA; Buxbaum, Sarah G SG; Boerwinkle, Eric E; Ballantyne, Christie M CM; Kathiresan, Sekar S; Rader, Daniel J DJ
Common variants at 12q14 and 12q24 are associated with hippocampal volume.
Nature Genetics
Bis, Joshua C JC; DeCarli, Charles C; Smith, Albert Vernon AV; van der Lijn, Fedde F; Crivello, Fabrice F; Fornage, Myriam M; Debette, Stephanie S; Shulman, Joshua M JM; Schmidt, Helena H; Srikanth, Velandai V; Schuur, Maaike M; Yu, Lei L; Choi, Seung-Hoan SH; Sigurdsson, Sigurdur S; Verhaaren, Benjamin F J BF; DeStefano, Anita L AL; Lambert, Jean-Charles JC; Jack, Clifford R CR; Struchalin, Maksim M; Stankovich, Jim J; Ibrahim-Verbaas, Carla A CA; Fleischman, Debra D; Zijdenbos, Alex A; den Heijer, Tom T; Mazoyer, Bernard B; Coker, Laura H LH; Enzinger, Christian C; Danoy, Patrick P; Amin, Najaf N; Arfanakis, Konstantinos K; van Buchem, Mark A MA; de Bruijn, Renée F A G RF; Beiser, Alexa A; Dufouil, Carole C; Huang, Juebin J; Cavalieri, Margherita M; Thomson, Russell R; Niessen, Wiro J WJ; Chibnik, Lori B LB; Gislason, Gauti K GK; Hofman, Albert A; Pikula, Aleksandra A; Amouyel, Philippe P; Freeman, Kevin B KB; Phan, Thanh G TG; Oostra, Ben A BA; Stein, Jason L JL; Medland, Sarah E SE; Vasquez, Alejandro Arias AA; Hibar, Derrek P DP; Wright, Margaret J MJ; Franke, Barbara B; Martin, Nicholas G NG; Thompson, Paul M PM; , ; Nalls, Michael A MA; Uitterlinden, Andre G AG; Au, Rhoda R; Elbaz, Alexis A; Beare, Richard J RJ; van Swieten, John C JC; Lopez, Oscar L OL; Harris, Tamara B TB; Chouraki, Vincent V; Breteler, Monique M B MM; De Jager, Philip L PL; Becker, James T JT; Vernooij, Meike W MW; Knopman, David D; Fazekas, Franz F; Wolf, Philip A PA; van der Lugt, Aad A; Gudnason, Vilmundur V; Longstreth, W T WT; Brown, Matthew A MA; Bennett, David A DA; van Duijn, Cornelia M CM; Mosley, Thomas H TH; Schmidt, Reinhold R; Tzourio, Christophe C; Launer, Lenore J LJ; Ikram, M Arfan MA; Seshadri, Sudha S; ,
Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease.
Molecular Psychiatry
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A comprehensive genetic association study of Alzheimer disease in African Americans.
Archives Of Neurology
Logue, Mark W MW; Schu, Matthew M; Vardarajan, Badri N BN; Buros, Jacki J; Green, Robert C RC; Go, Rodney C P RC; Griffith, Patrick P; Obisesan, Thomas O TO; Shatz, Rhonna R; Borenstein, Amy A; Cupples, L Adrienne LA; Lunetta, Kathryn L KL; Fallin, M Daniele MD; Baldwin, Clinton T CT; Farrer, Lindsay A LA; ,
The effect of TOMM40 poly-T length on gray matter volume and cognition in middle-aged persons with APOE ε3/ε3 genotype.
Alzheimer'S & Dementia : The Journal Of The Alzheimer'S Association
Johnson, Sterling C SC; La Rue, Asenath A; Hermann, Bruce P BP; Xu, Guofan G; Koscik, Rebecca L RL; Jonaitis, Erin M EM; Bendlin, Barbara B BB; Hogan, Kirk J KJ; Roses, Allen D AD; Saunders, Ann M AM; Lutz, Michael W MW; Asthana, Sanjay S; Green, Robert C RC; Sager, Mark A MA
TOMM40 poly-T variants and cerebrospinal fluid amyloid beta levels in the elderly.
Neurochemical Research
Pomara, Nunzio N; Bruno, Davide D; Nierenberg, Jay J JJ; Sidtis, John J JJ; Martiniuk, Frank T FT; Mehta, Pankaj D PD; Zetterberg, Henrik H; Blennow, Kaj K
Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease.
Plos One
Jones, Lesley L; Holmans, Peter A PA; Hamshere, Marian L ML; Harold, Denise D; Moskvina, Valentina V; Ivanov, Dobril D; Pocklington, Andrew A; Abraham, Richard R; Hollingworth, Paul P; Sims, Rebecca R; Gerrish, Amy A; Pahwa, Jaspreet Singh JS; Jones, Nicola N; Stretton, Alexandra A; Morgan, Angharad R AR; Lovestone, Simon S; Powell, John J; Proitsi, Petroula P; Lupton, Michelle K MK; Brayne, Carol C; Rubinsztein, David C DC; Gill, Michael M; Lawlor, Brian B; Lynch, Aoibhinn A; Morgan, Kevin K; Brown, Kristelle S KS; Passmore, Peter A PA; Craig, David D; McGuinness, Bernadette B; Todd, Stephen S; Holmes, Clive C; Mann, David D; Smith, A David AD; Love, Seth S; Kehoe, Patrick G PG; Mead, Simon S; Fox, Nick N; Rossor, Martin M; Collinge, John J; Maier, Wolfgang W; Jessen, Frank F; Schürmann, Britta B; Heun, Reinhard R; Kölsch, Heike H; van den Bussche, Hendrik H; Heuser, Isabella I; Peters, Oliver O; Kornhuber, Johannes J; Wiltfang, Jens J; Dichgans, Martin M; Frölich, Lutz L; Hampel, Harald H; Hüll, Michael M; Rujescu, Dan D; Goate, Alison M AM; Kauwe, John S K JS; Cruchaga, Carlos C; Nowotny, Petra P; Morris, John C JC; Mayo, Kevin K; Livingston, Gill G; Bass, Nicholas J NJ; Gurling, Hugh H; McQuillin, Andrew A; Gwilliam, Rhian R; Deloukas, Panos P; Al-Chalabi, Ammar A; Shaw, Christopher E CE; Singleton, Andrew B AB; Guerreiro, Rita R; Mühleisen, Thomas W TW; Nöthen, Markus M MM; Moebus, Susanne S; Jöckel, Karl-Heinz KH; Klopp, Norman N; Wichmann, H-Erich HE; Rüther, Eckhard E; Carrasquillo, Minerva M MM; Pankratz, V Shane VS; Younkin, Steven G SG; Hardy, John J; O'Donovan, Michael C MC; Owen, Michael J MJ; Williams, Julie J
Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities.
Plos Genetics
Naj, Adam C AC; Beecham, Gary W GW; Martin, Eden R ER; Gallins, Paul J PJ; Powell, Eric H EH; Konidari, Ioanna I; Whitehead, Patrice L PL; Cai, Guiqing G; Haroutunian, Vahram V; Scott, William K WK; Vance, Jeffery M JM; Slifer, Michael A MA; Gwirtsman, Harry E HE; Gilbert, John R JR; Haines, Jonathan L JL; Buxbaum, Joseph D JD; Pericak-Vance, Margaret A MA
A TOMM40 variable-length polymorphism predicts the age of late-onset Alzheimer's disease.
The Pharmacogenomics Journal
Roses, A D AD; Lutz, M W MW; Amrine-Madsen, H H; Saunders, A M AM; Crenshaw, D G DG; Sundseth, S S SS; Huentelman, M J MJ; Welsh-Bohmer, K A KA; Reiman, E M EM
Apolipoprotein E/C1 locus variants modify renal cell carcinoma risk.
Cancer Research
Moore, Lee E LE; Brennan, Paul P; Karami, Sara S; Menashe, Idan I; Berndt, Sonja I SI; Dong, Linda M LM; Meisner, Allison A; Yeager, Meredith M; Chanock, Stephen S; Colt, Joanne J; Schwartz, Kendra K; Davis, Faith F; Zaridze, David D; Mattveev, Vsevolod V; Janout, Vladimir V; Kollarova, Hellena H; Bencko, Vladimir V; Navratilova, Marie M; Szeszenia-Dabrowska, Neonilia N; Mates, Dana D; Holcatova, Ivana I; Boffetta, Paolo P; Chow, Wong-Ho WH; Rosenberg, Philip S PS; Rothman, Nathaniel N
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease.
Nature Genetics
Harold, Denise D; Abraham, Richard R; Hollingworth, Paul P; Sims, Rebecca R; Gerrish, Amy A; Hamshere, Marian L ML; Pahwa, Jaspreet Singh JS; Moskvina, Valentina V; Dowzell, Kimberley K; Williams, Amy A; Jones, Nicola N; Thomas, Charlene C; Stretton, Alexandra A; Morgan, Angharad R AR; Lovestone, Simon S; Powell, John J; Proitsi, Petroula P; Lupton, Michelle K MK; Brayne, Carol C; Rubinsztein, David C DC; Gill, Michael M; Lawlor, Brian B; Lynch, Aoibhinn A; Morgan, Kevin K; Brown, Kristelle S KS; Passmore, Peter A PA; Craig, David D; McGuinness, Bernadette B; Todd, Stephen S; Holmes, Clive C; Mann, David D; Smith, A David AD; Love, Seth S; Kehoe, Patrick G PG; Hardy, John J; Mead, Simon S; Fox, Nick N; Rossor, Martin M; Collinge, John J; Maier, Wolfgang W; Jessen, Frank F; Schürmann, Britta B; Heun, Reinhard R; van den Bussche, Hendrik H; Heuser, Isabella I; Kornhuber, Johannes J; Wiltfang, Jens J; Dichgans, Martin M; Frölich, Lutz L; Hampel, Harald H; Hüll, Michael M; Rujescu, Dan D; Goate, Alison M AM; Kauwe, John S K JS; Cruchaga, Carlos C; Nowotny, Petra P; Morris, John C JC; Mayo, Kevin K; Sleegers, Kristel K; Bettens, Karolien K; Engelborghs, Sebastiaan S; De Deyn, Peter P PP; Van Broeckhoven, Christine C; Livingston, Gill G; Bass, Nicholas J NJ; Gurling, Hugh H; McQuillin, Andrew A; Gwilliam, Rhian R; Deloukas, Panagiotis P; Al-Chalabi, Ammar A; Shaw, Christopher E CE; Tsolaki, Magda M; Singleton, Andrew B AB; Guerreiro, Rita R; Mühleisen, Thomas W TW; Nöthen, Markus M MM; Moebus, Susanne S; Jöckel, Karl-Heinz KH; Klopp, Norman N; Wichmann, H-Erich HE; Carrasquillo, Minerva M MM; Pankratz, V Shane VS; Younkin, Steven G SG; Holmans, Peter A PA; O'Donovan, Michael M; Owen, Michael J MJ; Williams, Julie J
Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.
Plos One
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