Publications:

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Polygenic risk score penetrance & recurrence risk in familial Alzheimer disease.

Annals Of Clinical And Translational Neurology

Qiao, Min M; Lee, Annie J AJ; Reyes-Dumeyer, Dolly D; Tosto, Giuseppe G; Faber, Kelley K; Goate, Alison A; Renton, Alan A; Chao, Michael M; Boeve, Brad B; Cruchaga, Carlos C; Pericak-Vance, Margaret M; Haines, Jonathan L JL; Rosenberg, Roger R; Tsuang, Debby D; Sweet, Robert A RA; Bennett, David A DA; Wilson, Robert S RS; Foroud, Tatiana T; Mayeux, Richard R; Vardarajan, Badri N BN

Publication Date: 2023-03-22

Variant appearance in text: rs769449

PubMed Link: 36946865

Variant Present in the following documents:

• Main text
• ACN3-10-744.pdf

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Characteristics of circulating small noncoding RNAs in plasma and serum during human aging.

Aging Medicine (Milton (N.S.W))

Xiao, Ping P; Shi, Zhangyue Z; Liu, Chenang C; Hagen, Darren E DE

Publication Date: 2023-03

Variant appearance in text: rs769449

PubMed Link: 36911092

Variant Present in the following documents:

• AGM2-6-35-s002.xlsx, sheet 3

View BVdb publication page

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Host Genetic Variants Linked to COVID-19 Neurological Complications and Susceptibility in Young Adults-A Preliminary Analysis.

Journal Of Personalized Medicine

Kazantseva, Anastasiya A; Enikeeva, Renata R; Takhirova, Zalina Z; Davydova, Yuliya Y; Mustafin, Rustam R; Malykh, Sergey S; Karunas, Alexandra A; Kanapin, Alexander A; Khusnutdinova, Elza E

Publication Date: 2023-01-06

Variant appearance in text: rs769449

PubMed Link: 36675784

Variant Present in the following documents:

• jpm-13-00123.pdf

View BVdb publication page

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Genetic studies of plasma analytes identify novel potential biomarkers for several complex traits.

Scientific Reports

Deming, Yuetiva Y; Xia, Jian J; Cai, Yefei Y; Lord, Jenny J; Del-Aguila, Jorge L JL; Fernandez, Maria Victoria MV; Carrell, David D; Black, Kathleen K; Budde, John J; Ma, ShengMei S; Saef, Benjamin B; Howells, Bill B; Bertelsen, Sarah S; Bailey, Matthew M; Ridge, Perry G PG; , ; Holtzman, David D; Morris, John C JC; Bales, Kelly K; Pickering, Eve H EH; Lee, Jin-Moo JM; Heitsch, Laura L; Kauwe, John J; Goate, Alison A; Piccio, Laura L; Cruchaga, Carlos C

Publication Date: 2016-01-04

Variant appearance in text: rs769449

PubMed Link: 36647296

Variant Present in the following documents:

• srep18092-s1.pdf
• srep18092.pdf

View BVdb publication page

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Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects.

Nature Communications

Krohn, Lynne L; Heilbron, Karl K; Blauwendraat, Cornelis C; Reynolds, Regina H RH; Yu, Eric E; Senkevich, Konstantin K; Rudakou, Uladzislau U; Estiar, Mehrdad A MA; Gustavsson, Emil K EK; Brolin, Kajsa K; Ruskey, Jennifer A JA; Freeman, Kathryn K; Asayesh, Farnaz F; Chia, Ruth R; Arnulf, Isabelle I; Hu, Michele T M MTM; Montplaisir, Jacques Y JY; Gagnon, Jean-François JF; Desautels, Alex A; Dauvilliers, Yves Y; Gigli, Gian Luigi GL; Valente, Mariarosaria M; Janes, Francesco F; Bernardini, Andrea A; Högl, Birgit B; Stefani, Ambra A; Ibrahim, Abubaker A; Šonka, Karel K; Kemlink, David D; Oertel, Wolfgang W; Janzen, Annette A; Plazzi, Giuseppe G; Biscarini, Francesco F; Antelmi, Elena E; Figorilli, Michela M; Puligheddu, Monica M; Mollenhauer, Brit B; Trenkwalder, Claudia C; Sixel-Döring, Friederike F; Cochen De Cock, Valérie V; Monaca, Christelle Charley CC; Heidbreder, Anna A; Ferini-Strambi, Luigi L; Dijkstra, Femke F; Viaene, Mineke M; Abril, Beatriz B; Boeve, Bradley F BF; , ; Scholz, Sonja W SW; Ryten, Mina M; Bandres-Ciga, Sara S; Noyce, Alastair A; Cannon, Paul P; Pihlstrøm, Lasse L; Nalls, Mike A MA; Singleton, Andrew B AB; Rouleau, Guy A GA; Postuma, Ronald B RB; Gan-Or, Ziv Z

Publication Date: 2022-12-05

Variant appearance in text: rs769449

PubMed Link: 36470867

Variant Present in the following documents:

• Main text
• 41467_2022_34732_MOESM2_ESM.pdf
• 41467_2022_Article_34732.pdf

View BVdb publication page

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Interpretable deep learning translation of GWAS and multi-omics findings to identify pathobiology and drug repurposing in Alzheimer's disease.

Cell Reports

Xu, Jielin J; Mao, Chengsheng C; Hou, Yuan Y; Luo, Yuan Y; Binder, Jessica L JL; Zhou, Yadi Y; Bekris, Lynn M LM; Shin, Jiyoung J; Hu, Ming M; Wang, Fei F; Eng, Charis C; Oprea, Tudor I TI; Flanagan, Margaret E ME; Pieper, Andrew A AA; Cummings, Jeffrey J; Leverenz, James B JB; Cheng, Feixiong F

Publication Date: 2022-11-29

Variant appearance in text: rs769449

PubMed Link: 36450252

Variant Present in the following documents:

• Main text
• nihms-1854082.pdf

View BVdb publication page

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The influence of 17q21.31 and APOE genetic ancestry on neurodegenerative disease risk.

Frontiers In Aging Neuroscience

Harerimana, Nadia V NV; Goate, Alison M AM; Bowles, Kathryn R KR

Publication Date: 2022

Variant appearance in text: rs769449

PubMed Link: 36337698

Variant Present in the following documents:

• Main text
• fnagi-14-1021918.pdf

View BVdb publication page

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APOE ɛ4 allele and TOMM40-APOC1 variants jointly contribute to survival to older ages.

Aging Cell

Kulminski, Alexander M AM; Jain-Washburn, Ethan E; Philipp, Ian I; He, Liang L; Loika, Yury Y; Loiko, Elena E; Bagley, Olivia O; Ukraintseva, Svetlana S; Yashin, Anatoliy A; Arbeev, Konstantin K; Stallard, Eric E; Feitosa, Mary F MF; Schupf, Nicole N; Christensen, Kaare K; Culminskaya, Irina I

Publication Date: 2022-11-03

Variant appearance in text: rs769449

PubMed Link: 36330582

Variant Present in the following documents:

• Main text
• ACEL-21-e13730.pdf

View BVdb publication page

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Exploring the role of non-coding RNAs as potential candidate biomarkers in the cross-talk between diabetes mellitus and Alzheimer's disease.

Frontiers In Aging Neuroscience

Ghiam, Shokoofeh S; Eslahchi, Changiz C; Shahpasand, Koorosh K; Habibi-Rezaei, Mehran M; Gharaghani, Sajjad S

Publication Date: 2022

Variant appearance in text: rs769449

PubMed Link: 36092798

Variant Present in the following documents:

• Main text
• fnagi-14-955461.pdf

View BVdb publication page

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A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts.

Human Genome Variation

Irum, Bushra B; Kabir, Firoz F; Shoshany, Nadav N; Khan, Shahid Y SY; Rauf, Bushra B; Naeem, Muhammad Asif MA; Qaiser, Tanveer A TA; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA

Publication Date: 2022-09-08

Variant appearance in text: rs769449

PubMed Link: 36075891

Variant Present in the following documents:

• 41439_2022_208_MOESM5_ESM.xlsx, sheet 2

View BVdb publication page

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TOMM40 genetic variants associated with healthy aging and longevity: a systematic review.

Bmc Geriatrics

Chen, Sunny S; Sarasua, Sara M SM; Davis, Nicole J NJ; DeLuca, Jane M JM; Boccuto, Luigi L; Thielke, Stephen M SM; Yu, Chang-En CE

Publication Date: 2022-08-13

Variant appearance in text: rs769449

PubMed Link: 35964003

Variant Present in the following documents:

• Main text
• 12877_2022_Article_3337.pdf

View BVdb publication page

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Inter- and intra-chromosomal modulators of the APOE ɛ2 and ɛ4 effects on the Alzheimer's disease risk.

Geroscience

Nazarian, Alireza A; Philipp, Ian I; Culminskaya, Irina I; He, Liang L; Kulminski, Alexander M AM

Publication Date: 2022-07-09

Variant appearance in text: rs769449

PubMed Link: 35809216

Variant Present in the following documents:

• Main text
• 11357_2022_Article_617.pdf

View BVdb publication page

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Brain Radiotoxicity-Related 15CAcBRT Gene Expression Signature Predicts Survival Prognosis of Glioblastoma Patients.

Neuro-Oncology

Reyes-González, Jesús J; Barajas-Olmos, Francisco F; García-Ortiz, Humberto H; Magraner-Pardo, Lorena L; Pons, Tirso T; Moreno, Sergio S; Aguirre-Cruz, Lucinda L; Reyes-Abrahantes, Andy A; Martínez-Hernández, Angélica A; Contreras-Cubas, Cecilia C; Barrios-Payan, Jorge J; Ruiz-Garcia, Henry J HJ; Hernandez-Pando, Rogelio R; Quiñones-Hinojosa, Alfredo A; Orozco, Lorena L; Abrahantes-Pérez, María Del Carmen MDC

Publication Date: 2022-07-08

Variant appearance in text: rs769449

PubMed Link: 35802478

Variant Present in the following documents:

• noac171_suppl_suplementary_table_s7.xlsx, sheet 1

View BVdb publication page

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Genome-Wide Association Study of Incident Dementia in a Community-Based Sample of Older Subjects.

Journal Of Alzheimer'S Disease : Jad

Harper, Jordan D JD; Fan, Kang-Hsien KH; Aslam, M Muaaz MM; Snitz, Beth E BE; DeKosky, Steven T ST; Lopez, Oscar L OL; Feingold, Eleanor E; Kamboh, M Ilyas MI

Publication Date: 2022

Variant appearance in text: rs769449

PubMed Link: 35694926

Variant Present in the following documents:

• Main text
• jad-88-jad220293.pdf

View BVdb publication page

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Genome- and epigenome-wide studies of plasma protein biomarkers for Alzheimer's disease implicate TBCA and TREM2 in disease risk.

Alzheimer'S & Dementia (Amsterdam, Netherlands)

Hillary, Robert F RF; Gadd, Danni A DA; McCartney, Daniel L DL; Shi, Liu L; Campbell, Archie A; Walker, Rosie M RM; Ritchie, Craig W CW; Deary, Ian J IJ; Evans, Kathryn L KL; Nevado-Holgado, Alejo J AJ; Hayward, Caroline C; Porteous, David J DJ; McIntosh, Andrew M AM; Lovestone, Simon S; Robinson, Matthew R MR; Marioni, Riccardo E RE

Publication Date: 2022

Variant appearance in text: rs769449

PubMed Link: 35475137

Variant Present in the following documents:

• Main text
• DAD2-14-e12280.pdf

View BVdb publication page

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Machine learning methods applied to genotyping data capture interactions between single nucleotide variants in late onset Alzheimer's disease.

Alzheimer'S & Dementia (Amsterdam, Netherlands)

Arnal Segura, Magdalena M; Bini, Giorgio G; Fernandez Orth, Dietmar D; Samaras, Eleftherios E; Kassis, Maya M; Aisopos, Fotis F; Rambla De Argila, Jordi J; Paliouras, George G; Garrard, Peter P; Giambartolomei, Claudia C; Tartaglia, Gian Gaetano GG

Publication Date: 2022

Variant appearance in text: rs769449

PubMed Link: 35415203

Variant Present in the following documents:

• Main text
• DAD2-14-e12300.pdf

View BVdb publication page

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APOE and KLF14 genetic variants are sex-specific for low high-density lipoprotein cholesterol identified by a genome-wide association study.

Genetics And Molecular Biology

Lee, Ying-Hui YH; Chang, Ya-Sian YS; Hsieh, Chih-Chang CC; Wang, Rong-Tsorng RT; Chang, Jan-Gowth JG; Chen, Chung-Jen CJ; Chang, Shun-Jen SJ

Publication Date: 2022

Variant appearance in text: rs769449

PubMed Link: 35238325

Variant Present in the following documents:

• Main text
• 1415-4757-GMB-45-1-e20210280.pdf

View BVdb publication page

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Increased brain volume from higher cereal and lower coffee intake: shared genetic determinants and impacts on cognition and metabolism.

Cerebral Cortex (New York, N.Y. : 1991)

Kang, Jujiao J; Jia, Tianye T; Jiao, Zeyu Z; Shen, Chun C; Xie, Chao C; Cheng, Wei W; Sahakian, Barbara J BJ; Waxman, David D; Feng, Jianfeng J

Publication Date: 2022-11-09

Variant appearance in text: rs769449

PubMed Link: 35136970

Variant Present in the following documents:

• supplementary_materials_revised_submit_bhac005.pdf

View BVdb publication page

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Genetic Regulatory Networks of Apolipoproteins and Associated Medical Risks.

Frontiers In Cardiovascular Medicine

Basavaraju, Preethi P; Balasubramani, Rubadevi R; Kathiresan, Divya Sri DS; Devaraj, Ilakkiyapavai I; Babu, Kavipriya K; Alagarsamy, Vasanthakumar V; Puthamohan, Vinayaga Moorthi VM

Publication Date: 2021

Variant appearance in text: rs769449

PubMed Link: 35071357

Variant Present in the following documents:

• Main text

View BVdb publication page

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Missing lnc(RNAs) in Alzheimer's Disease?

Genes

Policarpo, Rafaela R; d'Ydewalle, Constantin C

Publication Date: 2021-12-23

Variant appearance in text: rs769449

PubMed Link: 35052379

Variant Present in the following documents:

• Main text

View BVdb publication page

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Missing lnc(RNAs) in Alzheimer's Disease?

Genes

Policarpo, Rafaela R; d'Ydewalle, Constantin C

Publication Date: 2021-12-23

Variant appearance in text: rs769449

PubMed Link: 35052379

Variant Present in the following documents:

• Main text

View BVdb publication page

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Modulated anti-VEGF therapy under the influence of lipid metabolizing proteins in Age related macular degeneration: a pilot study.

Scientific Reports

Sharma, Kaushal K; Battu, Priya P; Singh, Ramandeep R; Sharma, Suresh Kumar SK; Anand, Akshay A

Publication Date: 2022-01-13

Variant appearance in text: rs769449

PubMed Link: 35027571

Variant Present in the following documents:

• Main text
• 41598_2021_Article_4269.pdf

View BVdb publication page

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Modulated anti-VEGF therapy under the influence of lipid metabolizing proteins in Age related macular degeneration: a pilot study.

Scientific Reports

Sharma, Kaushal K; Battu, Priya P; Singh, Ramandeep R; Sharma, Suresh Kumar SK; Anand, Akshay A

Publication Date: 2022-01-13

Variant appearance in text: rs769449

PubMed Link: 35027571

Variant Present in the following documents:

• Main text
• 41598_2021_Article_4269.pdf

View BVdb publication page

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Association between clinical symptoms and apolipoprotein A1 or apolipoprotein B levels is regulated by apolipoprotein E variant rs429358 in patients with chronic schizophrenia.

Annals Of General Psychiatry

Rao, Wenwang W; Meng, Xiangfei X; Li, Keqing K; Zhang, Yunshu Y; Zhang, Xiang Yang XY

Publication Date: 2021-12-20

Variant appearance in text: rs769449

PubMed Link: 34930329

Variant Present in the following documents:

• Main text
• 12991_2021_Article_376.pdf

View BVdb publication page

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Association between clinical symptoms and apolipoprotein A1 or apolipoprotein B levels is regulated by apolipoprotein E variant rs429358 in patients with chronic schizophrenia.

Annals Of General Psychiatry

Rao, Wenwang W; Meng, Xiangfei X; Li, Keqing K; Zhang, Yunshu Y; Zhang, Xiang Yang XY

Publication Date: 2021-12-20

Variant appearance in text: rs769449

PubMed Link: 34930329

Variant Present in the following documents:

• Main text
• 12991_2021_Article_376.pdf

View BVdb publication page

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Genome-wide analysis of common and rare variants via multiple knockoffs at biobank scale, with an application to Alzheimer disease genetics.

American Journal Of Human Genetics

He, Zihuai Z; Le Guen, Yann Y; Liu, Linxi L; Lee, Justin J; Ma, Shiyang S; Yang, Andrew C AC; Liu, Xiaoxia X; Rutledge, Jarod J; Losada, Patricia Moran PM; Song, Bowen B; Belloy, Michael E ME; Butler, Robert R RR; Longo, Frank M FM; Tang, Hua H; Mormino, Elizabeth C EC; Wyss-Coray, Tony T; Greicius, Michael D MD; Ionita-Laza, Iuliana I

Publication Date: 2021-12-02

Variant appearance in text: rs769449

PubMed Link: 34767756

Variant Present in the following documents:

• Main text
• main.pdf
• mmc2.pdf

View BVdb publication page

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Genome-wide analysis of common and rare variants via multiple knockoffs at biobank scale, with an application to Alzheimer disease genetics.

American Journal Of Human Genetics

He, Zihuai Z; Le Guen, Yann Y; Liu, Linxi L; Lee, Justin J; Ma, Shiyang S; Yang, Andrew C AC; Liu, Xiaoxia X; Rutledge, Jarod J; Losada, Patricia Moran PM; Song, Bowen B; Belloy, Michael E ME; Butler, Robert R RR; Longo, Frank M FM; Tang, Hua H; Mormino, Elizabeth C EC; Wyss-Coray, Tony T; Greicius, Michael D MD; Ionita-Laza, Iuliana I

Publication Date: 2021-12-02

Variant appearance in text: rs769449

PubMed Link: 34767756

Variant Present in the following documents:

• Main text
• main.pdf
• mmc2.pdf

View BVdb publication page

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Association and Gene-Gene Interactions Study of Late-Onset Alzheimer's Disease in the Russian Population.

Genes

Bocharova, Anna A; Vagaitseva, Kseniya K; Marusin, Andrey A; Zhukova, Natalia N; Zhukova, Irina I; Minaycheva, Larisa L; Makeeva, Oksana O; Stepanov, Vadim V

Publication Date: 2021-10-19

Variant appearance in text: rs769449

PubMed Link: 34681041

Variant Present in the following documents:

• Main text
• genes-12-01647.pdf

View BVdb publication page

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Analysis of genes (TMEM106B, GRN, ABCC9, KCNMB2, and APOE) implicated in risk for LATE-NC and hippocampal sclerosis provides pathogenetic insights: a retrospective genetic association study.

Acta Neuropathologica Communications

Dugan, Adam J AJ; Nelson, Peter T PT; Katsumata, Yuriko Y; Shade, Lincoln M P LMP; Boehme, Kevin L KL; Teylan, Merilee A MA; Cykowski, Matthew D MD; Mukherjee, Shubhabrata S; Kauwe, John S K JSK; Hohman, Timothy J TJ; Schneider, Julie A JA; , ; Fardo, David W DW

Publication Date: 2021-09-15

Variant appearance in text: rs769449

PubMed Link: 34526147

Variant Present in the following documents:

• Main text
• 40478_2021_Article_1250.pdf

View BVdb publication page

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Identifying Imaging Genetics Biomarkers of Alzheimer's Disease by Multi-Task Sparse Canonical Correlation Analysis and Regression.

Frontiers In Genetics

Ke, Fengchun F; Kong, Wei W; Wang, Shuaiqun S

Publication Date: 2021

Variant appearance in text: rs769449

PubMed Link: 34422007

Variant Present in the following documents:

• Main text
• fgene-12-706986.pdf

View BVdb publication page

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GWAS-Top Polymorphisms Associated With Late-Onset Alzheimer Disease in Brazil: Pointing Out Possible New Culprits Among Non-Coding RNAs.

Frontiers In Molecular Biosciences

Kretzschmar, Gabriela Canalli GC; Alencar, Nina Moura NM; da Silva, Saritha Suellen Lopes SSL; Sulzbach, Carla Daniela CD; Meissner, Caroline Grisbach CG; Petzl-Erler, Maria Luiza ML; Souza, Ricardo Lehtonen R RLR; Boldt, Angelica Beate Winter ABW

Publication Date: 2021

Variant appearance in text: rs769449

PubMed Link: 34291080

Variant Present in the following documents:

• Main text
• fmolb-08-632314.pdf

View BVdb publication page

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Sleeping pattern and activities of daily living modulate protein expression in AMD.

Plos One

Sharma, Kaushal K; Singh, Ramandeep R; Sharma, Suresh Kumar SK; Anand, Akshay A

Publication Date: 2021

Variant appearance in text: rs769449

PubMed Link: 34061866

Variant Present in the following documents:

• Main text

View BVdb publication page

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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

Publication Date: 2021-05-21

Variant appearance in text: rs769449

PubMed Link: 34020725

Variant Present in the following documents:

• 40478_2021_1199_MOESM1_ESM.pdf

View BVdb publication page

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A Mendelian randomization study of the role of lipoprotein subfractions in coronary artery disease.

Elife

Zhao, Qingyuan Q; Wang, Jingshu J; Miao, Zhen Z; Zhang, Nancy R NR; Hennessy, Sean S; Small, Dylan S DS; Rader, Daniel J DJ

Publication Date: 2021-04-26

Variant appearance in text: rs769449

PubMed Link: 33899735

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic Variability in Molecular Pathways Implicated in Alzheimer's Disease: A Comprehensive Review.

Frontiers In Aging Neuroscience

Vogrinc, David D; Goričar, Katja K; Dolžan, Vita V

Publication Date: 2021

Variant appearance in text: rs769449

PubMed Link: 33815092

Variant Present in the following documents:

• Main text
• fnagi-13-646901.pdf

View BVdb publication page

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Integrated genetic analyses revealed novel human longevity loci and reduced risks of multiple diseases in a cohort study of 15,651 Chinese individuals.

Aging Cell

Liu, Xiaomin X; Song, Zijun Z; Li, Yan Y; Yao, Yao Y; Fang, Mingyan M; Bai, Chen C; An, Peng P; Chen, Huashuai H; Chen, Zhihua Z; Tang, Biyao B; Shen, Juan J; Gao, Xiaotong X; Zhang, Mingrong M; Chen, Pengyu P; Zhang, Tao T; Jia, Huijue H; Liu, Xiao X; Hou, Yong Y; Yang, Huanming H; Wang, Jian J; Wang, Fudi F; Xu, Xun X; Min, Junxia J; Nie, Chao C; Zeng, Yi Y

Publication Date: 2021-03

Variant appearance in text: rs769449

PubMed Link: 33657282

Variant Present in the following documents:

• Main text
• ACEL-20-e13323-s014.xlsx, sheet 1

View BVdb publication page

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Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture.

Nature Genetics

Chia, Ruth R; Sabir, Marya S MS; Bandres-Ciga, Sara S; Saez-Atienzar, Sara S; Reynolds, Regina H RH; Gustavsson, Emil E; Walton, Ronald L RL; Ahmed, Sarah S; Viollet, Coralie C; Ding, Jinhui J; Makarious, Mary B MB; Diez-Fairen, Monica M; Portley, Makayla K MK; Shah, Zalak Z; Abramzon, Yevgeniya Y; Hernandez, Dena G DG; Blauwendraat, Cornelis C; Stone, David J DJ; Eicher, John J; Parkkinen, Laura L; Ansorge, Olaf O; Clark, Lorraine L; Honig, Lawrence S LS; Marder, Karen K; Lemstra, Afina A; St George-Hyslop, Peter P; Londos, Elisabet E; Morgan, Kevin K; Lashley, Tammaryn T; Warner, Thomas T TT; Jaunmuktane, Zane Z; Galasko, Douglas D; Santana, Isabel I; Tienari, Pentti J PJ; Myllykangas, Liisa L; Oinas, Minna M; Cairns, Nigel J NJ; Morris, John C JC; Halliday, Glenda M GM; Van Deerlin, Vivianna M VM; Trojanowski, John Q JQ; Grassano, Maurizio M; Calvo, Andrea A; Mora, Gabriele G; Canosa, Antonio A; Floris, Gianluca G; Bohannan, Ryan C RC; Brett, Francesca F; Gan-Or, Ziv Z; Geiger, Joshua T JT; Moore, Anni A; May, Patrick P; Krüger, Rejko R; Goldstein, David S DS; Lopez, Grisel G; Tayebi, Nahid N; Sidransky, Ellen E; , ; Norcliffe-Kaufmann, Lucy L; Palma, Jose-Alberto JA; Kaufmann, Horacio H; Shakkottai, Vikram G VG; Perkins, Matthew M; Newell, Kathy L KL; Gasser, Thomas T; Schulte, Claudia C; Landi, Francesco F; Salvi, Erika E; Cusi, Daniele D; Masliah, Eliezer E; Kim, Ronald C RC; Caraway, Chad A CA; Monuki, Edwin S ES; Brunetti, Maura M; Dawson, Ted M TM; Rosenthal, Liana S LS; Albert, Marilyn S MS; Pletnikova, Olga O; Troncoso, Juan C JC; Flanagan, Margaret E ME; Mao, Qinwen Q; Bigio, Eileen H EH; Rodríguez-Rodríguez, Eloy E; Infante, Jon J; Lage, Carmen C; González-Aramburu, Isabel I; Sanchez-Juan, Pascual P; Ghetti, Bernardino B; Keith, Julia J; Black, Sandra E SE; Masellis, Mario M; Rogaeva, Ekaterina E; Duyckaerts, Charles C; Brice, Alexis A; Lesage, Suzanne S; Xiromerisiou, Georgia G; Barrett, Matthew J MJ; Tilley, Bension S BS; Gentleman, Steve S; Logroscino, Giancarlo G; Serrano, Geidy E GE; Beach, Thomas G TG; McKeith, Ian G IG; Thomas, Alan J AJ; Attems, Johannes J; Morris, Christopher M CM; Palmer, Laura L; Love, Seth S; Troakes, Claire C; Al-Sarraj, Safa S; Hodges, Angela K AK; Aarsland, Dag D; Klein, Gregory G; Kaiser, Scott M SM; Woltjer, Randy R; Pastor, Pau P; Bekris, Lynn M LM; Leverenz, James B JB; Besser, Lilah M LM; Kuzma, Amanda A; Renton, Alan E AE; Goate, Alison A; Bennett, David A DA; Scherzer, Clemens R CR; Morris, Huw R HR; Ferrari, Raffaele R; Albani, Diego D; Pickering-Brown, Stuart S; Faber, Kelley K; Kukull, Walter A WA; Morenas-Rodriguez, Estrella E; Lleó, Alberto A; Fortea, Juan J; Alcolea, Daniel D; Clarimon, Jordi J; Nalls, Mike A MA; Ferrucci, Luigi L; Resnick, Susan M SM; Tanaka, Toshiko T; Foroud, Tatiana M TM; Graff-Radford, Neill R NR; Wszolek, Zbigniew K ZK; Ferman, Tanis T; Boeve, Bradley F BF; Hardy, John A JA; Topol, Eric J EJ; Torkamani, Ali A; Singleton, Andrew B AB; Ryten, Mina M; Dickson, Dennis W DW; Chiò, Adriano A; Ross, Owen A OA; Gibbs, J Raphael JR; Dalgard, Clifton L CL; Traynor, Bryan J BJ; Scholz, Sonja W SW

Publication Date: 2021-03

Variant appearance in text: rs769449

PubMed Link: 33589841

Variant Present in the following documents:

• Main text

View BVdb publication page

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Gene variants associated with obstructive sleep apnea (OSA) in relation to sudden infant death syndrome (SIDS).

International Journal Of Legal Medicine

Kerz, J J; Schürmann, P P; Rothämel, T T; Dörk, T T; Klintschar, M M

Publication Date: 2021-07

Variant appearance in text: rs769449

PubMed Link: 33559002

Variant Present in the following documents:

• Main text
• 414_2020_Article_2480.pdf

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Exome-Wide Association Study Identifies FN3KRP and PGP as New Candidate Longevity Genes.

The Journals Of Gerontology. Series A, Biological Sciences And Medical Sciences

Torres, Guillermo G GG; Nygaard, Marianne M; Caliebe, Amke A; Blanché, Hélène H; Chantalat, Sophie S; Galan, Pilar P; Lieb, Wolfgang W; Christiansen, Lene L; Deleuze, Jean-François JF; Christensen, Kaare K; Strauch, Konstantin K; Müller-Nurasyid, Martina M; Peters, Annette A; Nöthen, Markus M MM; Hoffmann, Per P; Flachsbart, Friederike F; Schreiber, Stefan S; Ellinghaus, David D; Franke, Andre A; Dose, Janina J; Nebel, Almut A

Publication Date: 2021-04-30

Variant appearance in text: rs769449

PubMed Link: 33491046

Variant Present in the following documents:

• Main text
• glab023.pdf

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Multivariate genome wide association and network analysis of subcortical imaging phenotypes in Alzheimer's disease.

Bmc Genomics

Meng, Xianglian X; Li, Jin J; Zhang, Qiushi Q; Chen, Feng F; Bian, Chenyuan C; Yao, Xiaohui X; Yan, Jingwen J; Xu, Zhe Z; Risacher, Shannon L SL; Saykin, Andrew J AJ; Liang, Hong H; Shen, Li L; ,

Publication Date: 2020-12-29

Variant appearance in text: rs769449

PubMed Link: 33372590

Variant Present in the following documents:

• Main text

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Genetic Variants behind Cardiovascular Diseases and Dementia.

Genes

Ho, Wei-Min WM; Wu, Yah-Yuan YY; Chen, Yi-Chun YC

Publication Date: 2020-12-18

Variant appearance in text: rs769449

PubMed Link: 33352859

Variant Present in the following documents:

• Main text

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APOE and Alzheimer's disease: advances in genetics, pathophysiology, and therapeutic approaches.

The Lancet. Neurology

Serrano-Pozo, Alberto A; Das, Sudeshna S; Hyman, Bradley T BT

Publication Date: 2021-01

Variant appearance in text: rs769449

PubMed Link: 33340485

Variant Present in the following documents:

• Main text
• nihms-1684246.pdf

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Functional genomic analyses uncover APOE-mediated regulation of brain and cerebrospinal fluid beta-amyloid levels in Parkinson disease.

Acta Neuropathologica Communications

Ibanez, Laura L; Bahena, Jorge A JA; Yang, Chengran C; Dube, Umber U; Farias, Fabiana H G FHG; Budde, John P JP; Bergmann, Kristy K; Brenner-Webster, Carol C; Morris, John C JC; Perrin, Richard J RJ; Cairns, Nigel J NJ; O'Donnell, John J; Álvarez, Ignacio I; Diez-Fairen, Monica M; Aguilar, Miquel M; Miller, Rebecca R; Davis, Albert A AA; Pastor, Pau P; Kotzbauer, Paul P; Campbell, Meghan C MC; Perlmutter, Joel S JS; Rhinn, Herve H; Harari, Oscar O; Cruchaga, Carlos C; Benitez, Bruno A BA

Publication Date: 2020-11-19

Variant appearance in text: rs769449

PubMed Link: 33213513

Variant Present in the following documents:

• Main text

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Genetic associations of in vivo pathology influence Alzheimer's disease susceptibility.

Alzheimer'S Research & Therapy

Seo, Jieun J; Byun, Min Soo MS; Yi, Dahyun D; Lee, Jun Ho JH; Jeon, So Yeon SY; Shin, Seong A SA; Kim, Yu Kyeong YK; Kang, Koung Mi KM; Sohn, Chul-Ho CH; Jung, Gijung G; Park, Jong-Chan JC; Han, Sun-Ho SH; Byun, Jayoung J; Mook-Jung, Inhee I; Lee, Dong Young DY; Choi, Murim M; ,

Publication Date: 2020-11-19

Variant appearance in text: rs769449

PubMed Link: 33213512

Variant Present in the following documents:

• Main text

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Matrix metalloproteinase-degraded type I collagen is associated with APOE/TOMM40 variants and preclinical dementia.

Neurology. Genetics

Tang, Man-Hung Eric ME; Blair, Joseph P M JPM; Bager, Cecilie Liv CL; Bay-Jensen, Anne-Christine AC; Henriksen, Kim K; Christiansen, Claus C; Karsdal, Morten Asser MA

Publication Date: 2020-10

Variant appearance in text: rs769449

PubMed Link: 33134509

Variant Present in the following documents:

• Main text
• NG2020014308.pdf

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