PCDH11X c.3034-62637A>G

Variant ID: X-91393737-A-G

NM_032968.3(PCDH11X):c.3034-62637A>G

This variant was identified in 19 publications

View GRCh38 version.




Publications:


Epigenetic mechanisms regulate sex-specific bias in disease manifestations.

Journal Of Molecular Medicine (Berlin, Germany)
Chlamydas, Sarantis S; Markouli, Mariam M; Strepkos, Dimitrios D; Piperi, Christina C
Publication Date: 2022-08

Variant appearance in text: rs5984894
PubMed Link: 35764820
Variant Present in the following documents:
  • Main text
  • 109_2022_Article_2227.pdf
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Sex Differences in Alzheimer's Disease: Insights From the Multiomics Landscape.

Biological Psychiatry
Guo, Lei L; Zhong, Margaret B MB; Zhang, Larry L; Zhang, Bin B; Cai, Dongming D
Publication Date: 2022-01-01

Variant appearance in text: rs5984894
PubMed Link: 33896621
Variant Present in the following documents:
  • Main text
  • nihms-1679133.pdf
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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: rs5984894
PubMed Link: 33815092
Variant Present in the following documents:
  • Main text
  • fnagi-13-646901.pdf
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The X Files: "The Mystery of X Chromosome Instability in Alzheimer's Disease".

Frontiers In Genetics
Bajic, Vladan P VP; Essack, Magbubah M; Zivkovic, Lada L; Stewart, Alan A; Zafirovic, Sonja S; Bajic, Vladimir B VB; Gojobori, Takashi T; Isenovic, Esma E; Spremo-Potparevic, Biljana B
Publication Date: 2019

Variant appearance in text: rs5984894
PubMed Link: 32047510
Variant Present in the following documents:
  • Main text
  • fgene-10-01368.pdf
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Genetic Heterogeneity of Alzheimer's Disease: Embracing Research Partnerships.

Journal Of Alzheimer'S Disease : Jad
Nacmias, Benedetta B; Bagnoli, Silvia S; Piaceri, Irene I; Sorbi, Sandro S
Publication Date: 2018

Variant appearance in text: rs5984894
PubMed Link: 29103034
Variant Present in the following documents:
  • Main text
  • jad-62-jad170570.pdf
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Unraveling the genes implicated in Alzheimer's disease.

Biomedical Reports
Giri, Mohan M; Shah, Abhilasha A; Upreti, Bibhuti B; Rai, Jayanti Chamling JC
Publication Date: 2017-08

Variant appearance in text: rs5984894
PubMed Link: 28781776
Variant Present in the following documents:
  • Main text
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Polygenic Analysis of Late-Onset Alzheimer's Disease from Mainland China.

Plos One
Jiao, Bin B; Liu, Xiaoyan X; Zhou, Lin L; Wang, Maggie Haitian MH; Zhou, Yafang Y; Xiao, Tingting T; Zhang, Weiwei W; Sun, Rui R; Waye, Mary Miu Yee MM; Tang, Beisha B; Shen, Lu L
Publication Date: 2015

Variant appearance in text: rs5984894
PubMed Link: 26680604
Variant Present in the following documents:
  • Main text
  • pone.0144898.pdf
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Candidate genes for Alzheimer's disease are associated with individual differences in plasma levels of beta amyloid peptides in adults with Down syndrome.

Neurobiology Of Aging
Schupf, Nicole N; Lee, Annie A; Park, Naeun N; Dang, Lam-Ha LH; Pang, Deborah D; Yale, Alexander A; Oh, David Kyung-Taek DK; Krinsky-McHale, Sharon J SJ; Jenkins, Edmund C EC; Luchsinger, José A JA; Zigman, Warren B WB; Silverman, Wayne W; Tycko, Benjamin B; Kisselev, Sergey S; Clark, Lorraine L; Lee, Joseph H JH
Publication Date: 2015-10

Variant appearance in text: rs5984894
PubMed Link: 26166206
Variant Present in the following documents:
  • Main text
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Replication study of genome-wide associated SNPs with late-onset Alzheimer's disease.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics
Burns, L C LC; Minster, R L RL; Demirci, F Y FY; Barmada, M M MM; Ganguli, M M; Lopez, O L OL; DeKosky, S T ST; Kamboh, M I MI
Publication Date: 2011-06

Variant appearance in text: rs5984894
PubMed Link: 21480501
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.

Nature Genetics
Naj, Adam C AC; Jun, Gyungah G; Beecham, Gary W GW; Wang, Li-San LS; Vardarajan, Badri Narayan BN; Buros, Jacqueline J; Gallins, Paul J PJ; Buxbaum, Joseph D JD; Jarvik, Gail P GP; Crane, Paul K PK; Larson, Eric B EB; Bird, Thomas D TD; Boeve, Bradley F BF; Graff-Radford, Neill R NR; De Jager, Philip L PL; Evans, Denis D; Schneider, Julie A JA; Carrasquillo, Minerva M MM; Ertekin-Taner, Nilufer N; Younkin, Steven G SG; Cruchaga, Carlos C; Kauwe, John S K JS; Nowotny, Petra P; Kramer, Patricia P; Hardy, John J; Huentelman, Matthew J MJ; Myers, Amanda J AJ; Barmada, Michael M MM; Demirci, F Yesim FY; Baldwin, Clinton T CT; Green, Robert C RC; Rogaeva, Ekaterina E; St George-Hyslop, Peter P; Arnold, Steven E SE; Barber, Robert R; Beach, Thomas T; Bigio, Eileen H EH; Bowen, James D JD; Boxer, Adam A; Burke, James R JR; Cairns, Nigel J NJ; Carlson, Chris S CS; Carney, Regina M RM; Carroll, Steven L SL; Chui, Helena C HC; Clark, David G DG; Corneveaux, Jason J; Cotman, Carl W CW; Cummings, Jeffrey L JL; DeCarli, Charles C; DeKosky, Steven T ST; Diaz-Arrastia, Ramon R; Dick, Malcolm M; Dickson, Dennis W DW; Ellis, William G WG; Faber, Kelley M KM; Fallon, Kenneth B KB; Farlow, Martin R MR; Ferris, Steven S; Frosch, Matthew P MP; Galasko, Douglas R DR; Ganguli, Mary M; Gearing, Marla M; Geschwind, Daniel H DH; Ghetti, Bernardino B; Gilbert, John R JR; Gilman, Sid S; Giordani, Bruno B; Glass, Jonathan D JD; Growdon, John H JH; Hamilton, Ronald L RL; Harrell, Lindy E LE; Head, Elizabeth E; Honig, Lawrence S LS; Hulette, Christine M CM; Hyman, Bradley T BT; Jicha, Gregory A GA; Jin, Lee-Way LW; Johnson, Nancy N; Karlawish, Jason J; Karydas, Anna A; Kaye, Jeffrey A JA; Kim, Ronald R; Koo, Edward H EH; Kowall, Neil W NW; Lah, James J JJ; Levey, Allan I AI; Lieberman, Andrew P AP; Lopez, Oscar L OL; Mack, Wendy J WJ; Marson, Daniel C DC; Martiniuk, Frank F; Mash, Deborah C DC; Masliah, Eliezer E; McCormick, Wayne C WC; McCurry, Susan M SM; McDavid, Andrew N AN; McKee, Ann C AC; Mesulam, Marsel M; Miller, Bruce L BL; Miller, Carol A CA; Miller, Joshua W JW; Parisi, Joseph E JE; Perl, Daniel P DP; Peskind, Elaine E; Petersen, Ronald C RC; Poon, Wayne W WW; Quinn, Joseph F JF; Rajbhandary, Ruchita A RA; Raskind, Murray M; Reisberg, Barry B; Ringman, John M JM; Roberson, Erik D ED; Rosenberg, Roger N RN; Sano, Mary M; Schneider, Lon S LS; Seeley, William W; Shelanski, Michael L ML; Slifer, Michael A MA; Smith, Charles D CD; Sonnen, Joshua A JA; Spina, Salvatore S; Stern, Robert A RA; Tanzi, Rudolph E RE; Trojanowski, John Q JQ; Troncoso, Juan C JC; Van Deerlin, Vivianna M VM; Vinters, Harry V HV; Vonsattel, Jean Paul JP; Weintraub, Sandra S; Welsh-Bohmer, Kathleen A KA; Williamson, Jennifer J; Woltjer, Randall L RL; Cantwell, Laura B LB; Dombroski, Beth A BA; Beekly, Duane D; Lunetta, Kathryn L KL; Martin, Eden R ER; Kamboh, M Ilyas MI; Saykin, Andrew J AJ; Reiman, Eric M EM; Bennett, David A DA; Morris, John C JC; Montine, Thomas J TJ; Goate, Alison M AM; Blacker, Deborah D; Tsuang, Debby W DW; Hakonarson, Hakon H; Kukull, Walter A WA; Foroud, Tatiana M TM; Haines, Jonathan L JL; Mayeux, Richard R; Pericak-Vance, Margaret A MA; Farrer, Lindsay A LA; Schellenberg, Gerard D GD
Publication Date: 2011-05

Variant appearance in text: rs5984894
PubMed Link: 21460841
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alzheimer's disease: diagnostics, prognostics and the road to prevention.

The Epma Journal
Grossman, Iris I; Lutz, Michael W MW; Crenshaw, Donna G DG; Saunders, Ann M AM; Burns, Daniel K DK; Roses, Allen D AD
Publication Date: 2010-06

Variant appearance in text: rs5984894
PubMed Link: 21124753
Variant Present in the following documents:
  • Main text
View BVdb publication page



The genetic architecture of Alzheimer's disease: beyond APP, PSENs and APOE.

Neurobiology Of Aging
Guerreiro, Rita J RJ; Gustafson, Deborah R DR; Hardy, John J
Publication Date: 2012-03

Variant appearance in text: rs5984894
PubMed Link: 20594621
Variant Present in the following documents:
  • Main text
View BVdb publication page



Intermediate phenotypes identify divergent pathways to Alzheimer's disease.

Plos One
Shulman, Joshua M JM; Chibnik, Lori B LB; Aubin, Cristin C; Schneider, Julie A JA; Bennett, David A DA; De Jager, Philip L PL
Publication Date: 2010-06-21

Variant appearance in text: rs5984894
PubMed Link: 20574532
Variant Present in the following documents:
  • Main text
  • pone.0011244.pdf
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PCDH11X variation is not associated with late-onset Alzheimer disease susceptibility.

Psychiatric Genetics
Beecham, Gary W GW; Naj, Adam C AC; Gilbert, John R JR; Haines, Jonathan L JL; Buxbaum, Joseph D JD; Pericak-Vance, Margaret A MA
Publication Date: 2010-12

Variant appearance in text: rs5984894
PubMed Link: 20523261
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetics of Alzheimer disease in the pre- and post-GWAS era.

Alzheimer'S Research & Therapy
Ertekin-Taner, Nilüfer N
Publication Date: 2010-03-05

Variant appearance in text: rs5984894
PubMed Link: 20236449
Variant Present in the following documents:
  • Main text
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Fine mapping of the chromosome 10q11-q21 linkage region in Alzheimer's disease cases and controls.

Neurogenetics
Fallin, Margaret Daniele MD; Szymanski, Megan M; Wang, Ruihua R; Gherman, Adrian A; Bassett, Susan S SS; Avramopoulos, Dimitrios D
Publication Date: 2010-07

Variant appearance in text: rs5984894
PubMed Link: 20182759
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association studies in Alzheimer's disease.

Human Molecular Genetics
Bertram, Lars L; Tanzi, Rudolph E RE
Publication Date: 2009-10-15

Variant appearance in text: rs5984894
PubMed Link: 19808789
Variant Present in the following documents:
  • Main text
View BVdb publication page



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
Publication Date: 2009-10

Variant appearance in text: rs5984894
PubMed Link: 19734902
Variant Present in the following documents:
  • Main text
  • ukmss-27833.pdf
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Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease.

Nature Genetics
Carrasquillo, Minerva M MM; Zou, Fanggeng F; Pankratz, V Shane VS; Wilcox, Samantha L SL; Ma, Li L; Walker, Louise P LP; Younkin, Samuel G SG; Younkin, Curtis S CS; Younkin, Linda H LH; Bisceglio, Gina D GD; Ertekin-Taner, Nilufer N; Crook, Julia E JE; Dickson, Dennis W DW; Petersen, Ronald C RC; Graff-Radford, Neill R NR; Younkin, Steven G SG
Publication Date: 2009-02

Variant appearance in text: rs5984894
PubMed Link: 19136949
Variant Present in the following documents:
  • Main text
View BVdb publication page