Publications:

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Complexity of Sex Differences and Their Impact on Alzheimer's Disease.

Biomedicines

Kadlecova, Marion M; Freude, Kristine K; Haukedal, Henriette H

Publication Date: 2023-04-24

Variant appearance in text: rs2282649

PubMed Link: 37238932

Variant Present in the following documents:

• biomedicines-11-01261.pdf

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Golgi fragmentation - One of the earliest organelle phenotypes in Alzheimer's disease neurons.

Frontiers In Neuroscience

Haukedal, Henriette H; Corsi, Giulia I GI; Gadekar, Veerendra P VP; Doncheva, Nadezhda T NT; Kedia, Shekhar S; de Haan, Noortje N; Chandrasekaran, Abinaya A; Jensen, Pia P; Schiønning, Pernille P; Vallin, Sarah S; Marlet, Frederik Ravnkilde FR; Poon, Anna A; Pires, Carlota C; Agha, Fawzi Khoder FK; Wandall, Hans H HH; Cirera, Susanna S; Simonsen, Anja Hviid AH; Nielsen, Troels Tolstrup TT; Nielsen, Jørgen Erik JE; Hyttel, Poul P; Muddashetty, Ravi R; Aldana, Blanca I BI; Gorodkin, Jan J; Nair, Deepak D; Meyer, Morten M; Larsen, Martin Røssel MR; Freude, Kristine K

Publication Date: 2023

Variant appearance in text: rs2282649

PubMed Link: 36875643

Variant Present in the following documents:

• Main text
• fnins-17-1120086.pdf

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Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem

Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS

Publication Date: 2022-11

Variant appearance in text: rs2282649

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

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JAK-STAT signaling in inflammatory breast cancer enables chemotherapy-resistant cell states.

Cancer Research

Stevens, Laura E LE; Peluffo, Guillermo G; Qiu, Xintao X; Temko, Daniel D; Fassl, Anne A; Li, Zheqi Z; Trinh, Anne A; Seehawer, Marco M; Jovanovic, Bojana B; Aleckovic, Masa M; Wilde, Callahan M CM; Geck, Renee C RC; Shu, Shaokun S; Kingston, Natalie L NL; Harper, Nicholas W NW; Almendro, Vanessa V; Pyke, Alanna L AL; Egri, Shawn B SB; Papanastasiou, Malvina M; Clement, Kendell K; Zhou, Ningxuan N; Walker, Sarah S; Salas, Jacqueline J; Park, So Yeon SY; Frank, David A DA; Meissner, Alexander A; Jaffe, Jacob D JD; Sicinski, Piotr P; Toker, Alex A; Michor, Franziska F; Long, Henry W HW; Overmoyer, Beth A BA; Polyak, Kornelia K

Publication Date: 2022-11-21

Variant appearance in text: SORL1: 5239+73C>T; rs2282649

PubMed Link: 36409824

Variant Present in the following documents:

• can-22-0423_supplementary_table_s3_suppst3.xlsx, sheet 1

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SORL1 Polymorphisms in Mexican Patients with Alzheimer's Disease.

Genes

Toral-Rios, Danira D; Ruiz-Sánchez, Elizabeth E; Rodríguez, Nancy Lucero Martínez NLM; Maury-Rosillo, Marlene M; Rosas-Carrasco, Óscar Ó; Becerril-Pérez, Fernando F; Mena-Barranco, Francisco F; Carvajal-García, Rosa R; Silva-Adaya, Daniela D; Delgado-Namorado, Yair Y; Ramos-Palacios, Gerardo G; Sánchez-Torres, Carmen C; Campos-Peña, Victoria V

Publication Date: 2022-03-25

Variant appearance in text: rs2282649

PubMed Link: 35456392

Variant Present in the following documents:

• Main text
• genes-13-00587.pdf

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Association between Alzheimer's disease genes and trajectories of cognitive function decline in Han Chinese in Taiwan.

Aging

Hsieh, Tsung-Jen TJ; Lee, Wei-Ju WJ; Liao, Yi-Chu YC; Hsu, Chih-Cheng CC; Fang, Yao-Hwei YH; Chen, Tzu-Yu TY; Lin, Yung-Shuan YS; Chang, I-Shou IS; Wang, Shuu-Jiun SJ; Hsiung, Chao A CA; Fuh, Jong-Ling JL; ,

Publication Date: 2021-07-02

Variant appearance in text: rs2282649

PubMed Link: 34214049

Variant Present in the following documents:

• Main text
• aging-13-203204.pdf

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Case Report: A Variant Non-ketotic Hyperglycinemia With GLRX5 Mutations: Manifestation of Deficiency of Activities of the Respiratory Chain Enzymes.

Frontiers In Genetics

Feng, Wei-Xing WX; Zhuo, Xiu-Wei XW; Liu, Zhi-Mei ZM; Li, Jiu-Wei JW; Zhang, Wei-Hua WH; Wu, Yun Y; Han, Tong-Li TL; Fang, Fang F

Publication Date: 2021

Variant appearance in text: SORL1: 5239+73C>T; rs2282649

PubMed Link: 34054912

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

View BVdb publication page

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Expression of an alternatively spliced variant of SORL1 in neuronal dendrites is decreased in patients with Alzheimer's disease.

Acta Neuropathologica Communications

Monti, Giulia G; Kjolby, Mads M; Jensen, Anne Mette G AMG; Allen, Mariet M; Reiche, Juliane J; Møller, Peter L PL; Comaposada-Baró, Raquel R; Zolkowski, Bartlomiej E BE; Vieira, Cármen C; Jørgensen, Margarita Melnikova MM; Holm, Ida E IE; Valdmanis, Paul N PN; Wellner, Niels N; Vægter, Christian B CB; Lincoln, Sarah J SJ; Nykjær, Anders A; Ertekin-Taner, Nilüfer N; Young, Jessica E JE; Nyegaard, Mette M; Andersen, Olav M OM

Publication Date: 2021-03-16

Variant appearance in text: rs2282649

PubMed Link: 33726851

Variant Present in the following documents:

• Main text
• 40478_2021_Article_1140.pdf

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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: rs2282649

PubMed Link: 33352859

Variant Present in the following documents:

• Main text
• genes-11-01514.pdf

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Cognitive Processing Speed Is Strongly Related to Driving Skills, Financial Abilities, and Other Instrumental Activities of Daily Living in Persons With Mild Cognitive Impairment and Mild Dementia.

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

Wadley, Virginia G VG; Bull, Tyler P TP; Zhang, Yue Y; Barba, Cheyanne C; Bryan, R Nick RN; Crowe, Michael M; Desiderio, Lisa L; Deutsch, Georg G; Erus, Guray G; Geldmacher, David S DS; Go, Rodney R; Lassen-Greene, Caroline L CL; Mamaeva, Olga A OA; Marson, Daniel C DC; McLaughlin, Marianne M; Nasrallah, Ilya M IM; Owsley, Cynthia C; Passler, Jesse J; Perry, Rodney T RT; Pilonieta, Giovanna G; Steward, Kayla A KA; Kennedy, Richard E RE

Publication Date: 2021-09-13

Variant appearance in text: rs2282649

PubMed Link: 33313639

Variant Present in the following documents:

• Main text

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Pharmacogenomics of Cognitive Dysfunction and Neuropsychiatric Disorders in Dementia.

International Journal Of Molecular Sciences

Cacabelos, Ramon R

Publication Date: 2020-04-26

Variant appearance in text: rs2282649

PubMed Link: 32357528

Variant Present in the following documents:

• Main text
• ijms-21-03059.pdf

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The Association Between Sortilin and Inflammation in Patients with Coronary Heart Disease.

Journal Of Inflammation Research

Han, Wenxiu W; Wei, Zhijie Z; Zhang, Hailiang H; Geng, Chunmei C; Dang, Ruili R; Yang, Mengqi M; Zhang, Jun J; Wang, Changshui C; Jiang, Pei P

Publication Date: 2020

Variant appearance in text: rs2282649

PubMed Link: 32104044

Variant Present in the following documents:

• Main text
• jir-13-71.pdf

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Mutant Huntingtin Affects Diabetes and Alzheimer's Markers in Human and Cell Models of Huntington's Disease.

Cells

Chaves, Gepoliano G; Stanley, John J; Pourmand, Nader N

Publication Date: 2019-08-23

Variant appearance in text: rs2282649

PubMed Link: 31450785

Variant Present in the following documents:

• cells-08-00962-s001.pdf

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Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology

Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P

Publication Date: 2018

Variant appearance in text: SORL1: 5239+73C>T; rs2282649

PubMed Link: 30319441

Variant Present in the following documents:

• Table_7.xlsx, sheet 1
• Table_5.xlsx, sheet 1
• Table_6.xlsx, sheet 1

View BVdb publication page

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Genetic Risk for Age-Related Cognitive Impairment Does Not Predict Cognitive Performance in Middle Age.

Journal Of Alzheimer'S Disease : Jad

Korthauer, Laura E LE; Awe, Elizabeth E; Frahmand, Marijam M; Driscoll, Ira I

Publication Date: 2018

Variant appearance in text: rs2282649

PubMed Link: 29865048

Variant Present in the following documents:

• Main text

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Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation

Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H

Publication Date: 2017

Variant appearance in text: rs2282649

PubMed Link: 28690861

Variant Present in the following documents:

• hgv201727-s1.xls, sheet 1

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Low statistical power in biomedical science: a review of three human research domains.

Royal Society Open Science

Dumas-Mallet, Estelle E; Button, Katherine S KS; Boraud, Thomas T; Gonon, Francois F; Munafò, Marcus R MR

Publication Date: 2017-02

Variant appearance in text: rs2282649

PubMed Link: 28386409

Variant Present in the following documents:

• rsos160254supp3.xlsx, sheet 1
• rsos160254supp3.xlsx, sheet 6

View BVdb publication page

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Clearance of cerebral Aβ in Alzheimer's disease: reassessing the role of microglia and monocytes.

Cellular And Molecular Life Sciences : Cmls

Zuroff, Leah L; Daley, David D; Black, Keith L KL; Koronyo-Hamaoui, Maya M

Publication Date: 2017-06

Variant appearance in text: rs2282649

PubMed Link: 28197669

Variant Present in the following documents:

• Main text

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SORL1 gene, plasma biomarkers, and the risk of Alzheimer's disease for the Han Chinese population in Taiwan.

Alzheimer'S Research & Therapy

Chou, Cheng-Ta CT; Liao, Yi-Chu YC; Lee, Wei-Ju WJ; Wang, Shuu-Jiun SJ; Fuh, Jong-Ling JL

Publication Date: 2016-12-30

Variant appearance in text: rs2282649

PubMed Link: 28034305

Variant Present in the following documents:

• Main text
• 13195_2016_Article_222.pdf

View BVdb publication page

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Replication Validity of Initial Association Studies: A Comparison between Psychiatry, Neurology and Four Somatic Diseases.

Plos One

Dumas-Mallet, Estelle E; Button, Katherine K; Boraud, Thomas T; Munafo, Marcus M; Gonon, François F

Publication Date: 2016

Variant appearance in text: rs2282649

PubMed Link: 27336301

Variant Present in the following documents:

• pone.0158064.s002.xlsx, sheet 5

View BVdb publication page

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Identifying genetic interactions associated with late-onset Alzheimer's disease.

Biodata Mining

Floudas, Charalampos S CS; Um, Nara N; Kamboh, M Ilyas MI; Barmada, Michael M MM; Visweswaran, Shyam S

Publication Date: 2014

Variant appearance in text: rs2282649

PubMed Link: 25649863

Variant Present in the following documents:

• Main text
• 13040_2014_Article_35.pdf

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Genetics of Alzheimer's disease in Caribbean Hispanic and African American populations.

Biological Psychiatry

Reitz, Christiane C; Mayeux, Richard R

Publication Date: 2014-04-01

Variant appearance in text: rs2282649

PubMed Link: 23890735

Variant Present in the following documents:

• Main text

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SORL1 is genetically associated with late-onset Alzheimer's disease in Japanese, Koreans and Caucasians.

Plos One

Miyashita, Akinori A; Koike, Asako A; Jun, Gyungah G; Wang, Li-San LS; Takahashi, Satoshi S; Matsubara, Etsuro E; Kawarabayashi, Takeshi T; Shoji, Mikio M; Tomita, Naoki N; Arai, Hiroyuki H; Asada, Takashi T; Harigaya, Yasuo Y; Ikeda, Masaki M; Amari, Masakuni M; Hanyu, Haruo H; Higuchi, Susumu S; Ikeuchi, Takeshi T; Nishizawa, Masatoyo M; Suga, Masaichi M; Kawase, Yasuhiro Y; Akatsu, Hiroyasu H; Kosaka, Kenji K; Yamamoto, Takayuki T; Imagawa, Masaki M; Hamaguchi, Tsuyoshi T; Yamada, Masahito M; Morihara, Takashi T; Moriaha, Takashi T; Takeda, Masatoshi M; Takao, Takeo T; Nakata, Kenji K; Fujisawa, Yoshikatsu Y; Sasaki, Ken K; Watanabe, Ken K; Nakashima, Kenji K; Urakami, Katsuya K; Ooya, Terumi T; Takahashi, Mitsuo M; Yuzuriha, Takefumi T; Serikawa, Kayoko K; Yoshimoto, Seishi S; Nakagawa, Ryuji R; Kim, Jong-Won JW; Ki, Chang-Seok CS; Won, Hong-Hee HH; Na, Duk L DL; Seo, Sang Won SW; Mook-Jung, Inhee I; , ; St George-Hyslop, Peter P; Mayeux, Richard R; Haines, Jonathan L JL; Pericak-Vance, Margaret A MA; Yoshida, Makiko M; Nishida, Nao N; Tokunaga, Katsushi K; Yamamoto, Ken K; Tsuji, Shoji S; Kanazawa, Ichiro I; Ihara, Yasuo Y; Schellenberg, Gerard D GD; Farrer, Lindsay A LA; Kuwano, Ryozo R

Publication Date: 2013

Variant appearance in text: rs2282649

PubMed Link: 23565137

Variant Present in the following documents:

• Main text
• pone.0058618.pdf

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Sortilin receptor 1 predicts longitudinal cognitive change.

Neurobiology Of Aging

Reynolds, Chandra A CA; Zavala, Catalina C; Gatz, Margaret M; Vie, Loryana L; Johansson, Boo B; Malmberg, Bo B; Ingelsson, Erik E; Prince, Jonathan A JA; Pedersen, Nancy L NL

Publication Date: 2013-06

Variant appearance in text: rs2282649

PubMed Link: 23318115

Variant Present in the following documents:

• Main text

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Genetics of subcortical vascular dementia.

Experimental Gerontology

Schmidt, Helena H; Freudenberger, Paul P; Seiler, Stephan S; Schmidt, Reinhold R

Publication Date: 2012-11

Variant appearance in text: rs2282649

PubMed Link: 22735669

Variant Present in the following documents:

• Main text

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Genetics of late-onset Alzheimer's disease: update from the alzgene database and analysis of shared pathways.

International Journal Of Alzheimer'S Disease

Olgiati, Paolo P; Politis, Antonis M AM; Papadimitriou, George N GN; De Ronchi, Diana D; Serretti, Alessandro A

Publication Date: 2011

Variant appearance in text: rs2282649

PubMed Link: 22191060

Variant Present in the following documents:

• Main text

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Impact of SORL1 single nucleotide polymorphisms on Alzheimer's disease cerebrospinal fluid markers.

Dementia And Geriatric Cognitive Disorders

Alexopoulos, Panagiotis P; Guo, Liang-Hao LH; Kratzer, Martina M; Westerteicher, Christine C; Kurz, Alexander A; Perneczky, Robert R

Publication Date: 2011

Variant appearance in text: rs2282649

PubMed Link: 21997402

Variant Present in the following documents:

• Main text

View BVdb publication page

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Neuroimaging measures as endophenotypes in Alzheimer's disease.

International Journal Of Alzheimer'S Disease

Braskie, Meredith N MN; Ringman, John M JM; Thompson, Paul M PM

Publication Date: 2011-03-31

Variant appearance in text: rs2282649

PubMed Link: 21547229

Variant Present in the following documents:

• Main text
• IJAD2011-490140.pdf

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Whole genome association analysis shows that ACE is a risk factor for Alzheimer's disease and fails to replicate most candidates from Meta-analysis.

International Journal Of Molecular Epidemiology And Genetics

Webster, Jennifer J; Reiman, Eric M EM; Zismann, Victoria L VL; Joshipura, Keta D KD; Pearson, John V JV; Hu-Lince, Diane D; Huentelman, Matthew J MJ; Craig, David W DW; Coon, Keith D KD; Beach, Thomas T; Rohrer, Kristen C KC; Zhao, Alice S AS; Leung, Doris D; Bryden, Leslie L; Marlowe, Lauren L; Kaleem, Mona M; Mastroeni, Diego D; Grover, Andrew A; Rogers, Joseph J; Heun, Reinhard R; Jessen, Frank F; Kölsch, Heike H; Heward, Christopher B CB; Ravid, Rivka R; Hutton, Michael L ML; Melquist, Stacey S; Petersen, Ron C RC; Caselli, Richard J RJ; Papassotiropoulos, Andreas A; Stephan, Dietrich A DA; Hardy, John J; Myers, Amanda A

Publication Date: 2010

Variant appearance in text: rs2282649

PubMed Link: 21537449

Variant Present in the following documents:

• Main text

View BVdb publication page

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Meta-analysis of the association between variants in SORL1 and Alzheimer disease.

Archives Of Neurology

Reitz, Christiane C; Cheng, Rong R; Rogaeva, Ekaterina E; Lee, Joseph H JH; Tokuhiro, Shinya S; Zou, Fanggeng F; Bettens, Karolien K; Sleegers, Kristel K; Tan, Eng King EK; Kimura, Ryo R; Shibata, Nobuto N; Arai, Heii H; Kamboh, M Ilyas MI; Prince, Jonathan A JA; Maier, Wolfgang W; Riemenschneider, Matthias M; Owen, Michael M; Harold, Denise D; Hollingworth, Paul P; Cellini, Elena E; Sorbi, Sandro S; Nacmias, Benedetta B; Takeda, Masatoshi M; Pericak-Vance, Margaret A MA; Haines, Jonathan L JL; Younkin, Steven S; Williams, Julie J; van Broeckhoven, Christine C; Farrer, Lindsay A LA; St George-Hyslop, Peter H PH; Mayeux, Richard R; ,

Publication Date: 2011-01

Variant appearance in text: rs2282649

PubMed Link: 21220680

Variant Present in the following documents:

• Main text

View BVdb publication page

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Validating predicted biological effects of Alzheimer's disease associated SNPs using CSF biomarker levels.

Journal Of Alzheimer'S Disease : Jad

Kauwe, John S K JS; Cruchaga, Carlos C; Bertelsen, Sarah S; Mayo, Kevin K; Latu, Wayne W; Nowotny, Petra P; Hinrichs, Anthony L AL; Fagan, Anne M AM; Holtzman, David M DM; , ; Goate, Alison M AM

Publication Date: 2010

Variant appearance in text: rs2282649

PubMed Link: 20634593

Variant Present in the following documents:

• Main text

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Use of genetic variation as biomarkers for mild cognitive impairment and progression of mild cognitive impairment to dementia.

Journal Of Alzheimer'S Disease : Jad

Reitz, Christiane C; Mayeux, Richard R

Publication Date: 2010

Variant appearance in text: rs2282649

PubMed Link: 20061642

Variant Present in the following documents:

• Main text

View BVdb publication page

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Use of genetic variation as biomarkers for Alzheimer's disease.

Annals Of The New York Academy Of Sciences

Reitz, Christiane C; Mayeux, Richard R

Publication Date: 2009-10

Variant appearance in text: rs2282649

PubMed Link: 19906263

Variant Present in the following documents:

• Main text

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Sequence variation in SORL1 and dementia risk in Swedes.

Neurogenetics

Reynolds, Chandra A CA; Hong, Mun-Gwan MG; Eriksson, Ulrika K UK; Blennow, Kaj K; Johansson, Boo B; Malmberg, Bo B; Berg, Stig S; Gatz, Margaret M; Pedersen, Nancy L NL; Bennet, Anna M AM; Prince, Jonathan A JA

Publication Date: 2010-02

Variant appearance in text: rs2282649

PubMed Link: 19653016

Variant Present in the following documents:

• Main text

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Endophenotypes in normal brain morphology and Alzheimer's disease: a review.

Neuroscience

Reitz, C C; Mayeux, R R

Publication Date: 2009-11-24

Variant appearance in text: rs2282649

PubMed Link: 19362127

Variant Present in the following documents:

• Main text

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Association of distinct variants in SORL1 with cerebrovascular and neurodegenerative changes related to Alzheimer disease.

Archives Of Neurology

T Cuenco, Karen K; Lunetta, Kathryn L KL; Baldwin, Clinton T CT; McKee, Ann C AC; Guo, Jianping J; Cupples, L Adrienne LA; Green, Robert C RC; St George-Hyslop, Peter H PH; Chui, Helena H; DeCarli, Charles C; Farrer, Lindsay A LA; ,

Publication Date: 2008-12

Variant appearance in text: rs2282649

PubMed Link: 19064752

Variant Present in the following documents:

• Main text

View BVdb publication page

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Possible association between SORL1 and Alzheimer disease? Reanalysing the data of Shibata et al.

Dementia And Geriatric Cognitive Disorders

Lee, Joseph H JH; Shibata, Nobuto N; Cheng, Rong R; Mayeux, Richard R

Publication Date: 2008

Variant appearance in text: rs2282649

PubMed Link: 18984959

Variant Present in the following documents:

• Main text

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Evaluation of the potential excess of statistically significant findings in published genetic association studies: application to Alzheimer's disease.

American Journal Of Epidemiology

Kavvoura, Fotini K FK; McQueen, Matthew B MB; Khoury, Muin J MJ; Tanzi, Rudolph E RE; Bertram, Lars L; Ioannidis, John P A JP

Publication Date: 2008-10-15

Variant appearance in text: rs2282649

PubMed Link: 18779388

Variant Present in the following documents:

• Main text

View BVdb publication page

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The neuronal sortilin-related receptor gene SORL1 and late-onset Alzheimer's disease.

Current Neurology And Neuroscience Reports

Lee, Joseph H JH; Barral, Sandra S; Reitz, Christiane C

Publication Date: 2008-09

Variant appearance in text: rs2282649

PubMed Link: 18713574

Variant Present in the following documents:

• Main text

View BVdb publication page

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Association between SORL1 and Alzheimer's disease in a genome-wide study.

Neuroreport

Meng, Yan Y; Lee, Joseph H JH; Cheng, Rong R; St George-Hyslop, Peter P; Mayeux, Richard R; Farrer, Lindsay A LA

Publication Date: 2007-11-19

Variant appearance in text: rs2282649

PubMed Link: 18090307

Variant Present in the following documents:

• Main text

View BVdb publication page

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Association between genetic variants in SORL1 and autopsy-confirmed Alzheimer disease.

Neurology

Lee, J H JH; Cheng, R R; Honig, L S LS; Vonsattel, J-P G JP; Clark, L L; Mayeux, R R

Publication Date: 2008-03-11

Variant appearance in text: rs2282649

PubMed Link: 17978276

Variant Present in the following documents:

• Main text

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SORL1 variants and risk of late-onset Alzheimer's disease.

Neurobiology Of Disease

Li, Yonghong Y; Rowland, Charles C; Catanese, Joseph J; Morris, John J; Lovestone, Simon S; O'Donovan, Michael C MC; Goate, Alison A; Owen, Michael M; Williams, Julie J; Grupe, Andrew A

Publication Date: 2008-02

Variant appearance in text: rs2282649

PubMed Link: 17949987

Variant Present in the following documents:

• Main text

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Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.

Bmc Medical Genetics

Seshadri, Sudha S; DeStefano, Anita L AL; Au, Rhoda R; Massaro, Joseph M JM; Beiser, Alexa S AS; Kelly-Hayes, Margaret M; Kase, Carlos S CS; D'Agostino, Ralph B RB; Decarli, Charles C; Atwood, Larry D LD; Wolf, Philip A PA

Publication Date: 2007-09-19

Variant appearance in text: rs2282649

PubMed Link: 17903297

Variant Present in the following documents:

• Main text

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Association between genetic variants in sortilin-related receptor 1 (SORL1) and Alzheimer's disease in adults with Down syndrome.

Neuroscience Letters

Lee, Joseph H JH; Chulikavit, Maruit M; Pang, Deborah D; Zigman, Warren B WB; Silverman, Wayne W; Schupf, Nicole N

Publication Date: 2007-09-25

Variant appearance in text: rs2282649

PubMed Link: 17826910

Variant Present in the following documents:

• Main text

View BVdb publication page

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The diploid genome sequence of an individual human.

Plos Biology

Levy, Samuel S; Sutton, Granger G; Ng, Pauline C PC; Feuk, Lars L; Halpern, Aaron L AL; Walenz, Brian P BP; Axelrod, Nelson N; Huang, Jiaqi J; Kirkness, Ewen F EF; Denisov, Gennady G; Lin, Yuan Y; MacDonald, Jeffrey R JR; Pang, Andy Wing Chun AW; Shago, Mary M; Stockwell, Timothy B TB; Tsiamouri, Alexia A; Bafna, Vineet V; Bansal, Vikas V; Kravitz, Saul A SA; Busam, Dana A DA; Beeson, Karen Y KY; McIntosh, Tina C TC; Remington, Karin A KA; Abril, Josep F JF; Gill, John J; Borman, Jon J; Rogers, Yu-Hui YH; Frazier, Marvin E ME; Scherer, Stephen W SW; Strausberg, Robert L RL; Venter, J Craig JC

Publication Date: 2007-09-04

Variant appearance in text: rs2282649

PubMed Link: 17803354

Variant Present in the following documents:

• pbio.0050254.pdf

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The association between genetic variants in SORL1 and Alzheimer disease in an urban, multiethnic, community-based cohort.

Archives Of Neurology

Lee, Joseph H JH; Cheng, Rong R; Schupf, Nicole N; Manly, Jennifer J; Lantigua, Rafael R; Stern, Yaakov Y; Rogaeva, Ekaterina E; Wakutani, Yosuke Y; Farrer, Lindsay L; St George-Hyslop, Peter P; Mayeux, Richard R

Publication Date: 2007-04

Variant appearance in text: rs2282649

PubMed Link: 17420311

Variant Present in the following documents:

• Main text

View BVdb publication page

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The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease.

Nature Genetics

Rogaeva, Ekaterina E; Meng, Yan Y; Lee, Joseph H JH; Gu, Yongjun Y; Kawarai, Toshitaka T; Zou, Fanggeng F; Katayama, Taiichi T; Baldwin, Clinton T CT; Cheng, Rong R; Hasegawa, Hiroshi H; Chen, Fusheng F; Shibata, Nobuto N; Lunetta, Kathryn L KL; Pardossi-Piquard, Raphaelle R; Bohm, Christopher C; Wakutani, Yosuke Y; Cupples, L Adrienne LA; Cuenco, Karen T KT; Green, Robert C RC; Pinessi, Lorenzo L; Rainero, Innocenzo I; Sorbi, Sandro S; Bruni, Amalia A; Duara, Ranjan R; Friedland, Robert P RP; Inzelberg, Rivka R; Hampe, Wolfgang W; Bujo, Hideaki H; Song, You-Qiang YQ; Andersen, Olav M OM; Willnow, Thomas E TE; Graff-Radford, Neill N; Petersen, Ronald C RC; Dickson, Dennis D; Der, Sandy D SD; Fraser, Paul E PE; Schmitt-Ulms, Gerold G; Younkin, Steven S; Mayeux, Richard R; Farrer, Lindsay A LA; St George-Hyslop, Peter P

Publication Date: 2007-02

Variant appearance in text: rs2282649

PubMed Link: 17220890

Variant Present in the following documents:

• Main text

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