MAPK1 c.857-3854A>C

Variant ID: 22-22131125-T-G

NM_002745.4(MAPK1):c.857-3854A>C

This variant was identified in 28 publications

View GRCh38 version.




Publications:


COVID-19: Focusing on the Link between Inflammation, Vitamin D, MAPK Pathway and Oxidative Stress Genetics.

Antioxidants (Basel, Switzerland)
Cusato, Jessica J; Manca, Alessandra A; Palermiti, Alice A; Mula, Jacopo J; Costanzo, Martina M; Antonucci, Miriam M; Chiara, Francesco F; De Vivo, Elisa Delia ED; Maiese, Domenico D; Ferrara, Micol M; Bonora, Stefano S; Di Perri, Giovanni G; D'Avolio, Antonio A; Calcagno, Andrea A
Publication Date: 2023-05-20

Variant appearance in text: rs2283792
PubMed Link: 37237997
Variant Present in the following documents:
  • Main text
  • antioxidants-12-01133.pdf
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Mutational landscape of gastric adenocarcinoma in Latin America: A genetic approach for precision medicine.

Genes & Diseases
Cerrato-Izaguirre, Dennis D; Chirino, Yolanda I YI; García-Cuellar, Claudia M CM; Santibáñez-Andrade, Miguel M; Prada, Diddier D; Hernández-Guerrero, Angélica A; Larraga, Octavio Alonso OA; Camacho, Javier J; Sánchez-Pérez, Yesennia Y
Publication Date: 2022-07

Variant appearance in text: rs2283792
PubMed Link: 35685475
Variant Present in the following documents:
  • Main text
  • main.pdf
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Identification of Genetic Networks Reveals Complex Associations and Risk Trajectory Linking Mild Cognitive Impairment to Alzheimer's Disease.

Frontiers In Aging Neuroscience
Strafella, Claudia C; Caputo, Valerio V; Termine, Andrea A; Fabrizio, Carlo C; Calvino, Giulia G; Megalizzi, Domenica D; Ruffo, Paola P; Toppi, Elisa E; Banaj, Nerisa N; Bassi, Andrea A; Bossù, Paola P; Caltagirone, Carlo C; Spalletta, Gianfranco G; Giardina, Emiliano E; Cascella, Raffaella R
Publication Date: 2022

Variant appearance in text: rs2283792
PubMed Link: 35250545
Variant Present in the following documents:
  • Main text
  • fnagi-14-821789.pdf
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Helicobacter pylori in Human Stomach: The Inconsistencies in Clinical Outcomes and the Probable Causes.

Frontiers In Microbiology
Alexander, Sneha Mary SM; Retnakumar, Radhakrishnan Jayalakshmi RJ; Chouhan, Deepak D; Devi, Thillai Natarajan Barani TNB; Dharmaseelan, Sanjai S; Devadas, Krishnadas K; Thapa, Namrata N; Tamang, Jyoti Prakash JP; Lamtha, Sangey Chhophel SC; Chattopadhyay, Santanu S
Publication Date: 2021

Variant appearance in text: rs2283792
PubMed Link: 34484153
Variant Present in the following documents:
  • Main text
  • fmicb-12-713955.pdf
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Immune System and Neuroinflammation in Idiopathic Parkinson's Disease: Association Analysis of Genetic Variants and miRNAs Interactions.

Frontiers In Genetics
Strafella, Claudia C; Caputo, Valerio V; Termine, Andrea A; Assogna, Francesca F; Pellicano, Clelia C; Pontieri, Francesco E FE; Macchiusi, Lucia L; Minozzi, Giulietta G; Gambardella, Stefano S; Centonze, Diego D; Bossù, Paola P; Spalletta, Gianfranco G; Caltagirone, Carlo C; Giardina, Emiliano E; Cascella, Raffaella R
Publication Date: 2021

Variant appearance in text: rs2283792
PubMed Link: 34149802
Variant Present in the following documents:
  • Main text
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Genetic Determinants Highlight the Existence of Shared Etiopathogenetic Mechanisms Characterizing Age-Related Macular Degeneration and Neurodegenerative Disorders.

Frontiers In Neurology
Strafella, Claudia C; Caputo, Valerio V; Termine, Andrea A; Fabrizio, Carlo C; Ruffo, Paola P; Potenza, Saverio S; Cusumano, Andrea A; Ricci, Federico F; Caltagirone, Carlo C; Giardina, Emiliano E; Cascella, Raffaella R
Publication Date: 2021

Variant appearance in text: rs2283792
PubMed Link: 34135841
Variant Present in the following documents:
  • Main text
  • fneur-12-626066.pdf
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Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.

Jci Insight
Chen, Xiao-Feng XF; Guo, Ming-Rui MR; Duan, Yuan-Yuan YY; Jiang, Feng F; Wu, Hao H; Dong, Shan-Shan SS; Zhou, Xiao-Rong XR; Thynn, Hlaing Nwe HN; Liu, Cong-Cong CC; Zhang, Lin L; Guo, Yan Y; Yang, Tie-Lin TL
Publication Date: 2020-09-03

Variant appearance in text: rs2283792
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
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Factors associated with relapses in relapsing-remitting multiple sclerosis: A systematic review and meta-analysis.

Medicine
Xie, Yao Y; Tian, Ziyu Z; Han, Fang F; Liang, Shibing S; Gao, Ying Y; Wu, Dahua D
Publication Date: 2020-07-02

Variant appearance in text: rs2283792
PubMed Link: 32629678
Variant Present in the following documents:
  • medi-99-e20885.pdf
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Polymorphisms in RAS/RAF/MEK/ERK Pathway Are Associated with Gastric Cancer.

Genes
Gonzalez-Hormazabal, Patricio P; Musleh, Maher M; Bustamante, Marco M; Stambuk, Juan J; Pisano, Raul R; Valladares, Hector H; Lanzarini, Enrique E; Chiong, Hector H; Rojas, Jorge J; Suazo, Jose J; Castro, V Gonzalo VG; Jara, Lilian L; Berger, Zoltan Z
Publication Date: 2018-12-28

Variant appearance in text: MAPK1: 857-3854A>C; rs2283792
PubMed Link: 30597917
Variant Present in the following documents:
  • Main text
  • genes-10-00020.pdf
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Shared Genetic Etiology of Autoimmune Diseases in Patients from a Biorepository Linked to De-identified Electronic Health Records.

Frontiers In Genetics
Restrepo, Nicole A NA; Butkiewicz, Mariusz M; McGrath, Josephine A JA; Crawford, Dana C DC
Publication Date: 2016

Variant appearance in text: rs2283792
PubMed Link: 27812365
Variant Present in the following documents:
  • Main text
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A Risk Score for Predicting Multiple Sclerosis.

Plos One
Dobson, Ruth R; Ramagopalan, Sreeram S; Topping, Joanne J; Smith, Paul P; Solanky, Bhavana B; Schmierer, Klaus K; Chard, Declan D; Giovannoni, Gavin G
Publication Date: 2016

Variant appearance in text: rs2283792
PubMed Link: 27802296
Variant Present in the following documents:
  • Main text
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Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies.

Neurology. Genetics
George, Michaela F MF; Briggs, Farren B S FB; Shao, Xiaorong X; Gianfrancesco, Milena A MA; Kockum, Ingrid I; Harbo, Hanne F HF; Celius, Elisabeth G EG; Bos, Steffan D SD; Hedström, Anna A; Shen, Ling L; Bernstein, Allan A; Alfredsson, Lars L; Hillert, Jan J; Olsson, Tomas T; Patsopoulos, Nikolaos A NA; De Jager, Philip L PL; Oturai, Annette B AB; Søndergaard, Helle B HB; Sellebjerg, Finn F; Sorensen, Per S PS; Gomez, Refujia R; Caillier, Stacy J SJ; Cree, Bruce A C BA; Oksenberg, Jorge R JR; Hauser, Stephen L SL; D'Alfonso, Sandra S; Leone, Maurizio A MA; Martinelli Boneschi, Filippo F; Sorosina, Melissa M; van der Mei, Ingrid I; Taylor, Bruce V BV; Zhou, Yuan Y; Schaefer, Catherine C; Barcellos, Lisa F LF
Publication Date: 2016-08

Variant appearance in text: rs2283792
PubMed Link: 27540591
Variant Present in the following documents:
  • NG2015001412.pdf
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Impact of polymorphisms in microRNA biogenesis genes on colon cancer risk and microRNA expression levels: a population-based, case-control study.

Bmc Medical Genomics
Mullany, Lila E LE; Herrick, Jennifer S JS; Wolff, Roger K RK; Buas, Matthew F MF; Slattery, Martha L ML
Publication Date: 2016-04-23

Variant appearance in text: rs2283792
PubMed Link: 27107574
Variant Present in the following documents:
  • Main text
  • 12920_2016_Article_181.pdf
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Translational utility of experimental autoimmune encephalomyelitis: recent developments.

Journal Of Inflammation Research
Guerreiro-Cacais, Andre Ortlieb AO; Laaksonen, Hannes H; Flytzani, Sevasti S; N'diaye, Marie M; Olsson, Tomas T; Jagodic, Maja M
Publication Date: 2015

Variant appearance in text: rs2283792
PubMed Link: 26622189
Variant Present in the following documents:
  • Main text
  • jir-8-211.pdf
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Combinations of susceptibility genes are associated with higher risk for multiple sclerosis and imply disease course specificity.

Plos One
Akkad, Denis A DA; Olischewsky, Alexandra A; Reiner, Franziska F; Hellwig, Kerstin K; Esser, Sarika S; Epplen, Jörg T JT; Curk, Tomaz T; Gold, Ralf R; Haghikia, Aiden A
Publication Date: 2015

Variant appearance in text: rs2283792
PubMed Link: 26011527
Variant Present in the following documents:
  • Main text
  • pone.0127632.pdf
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Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy.

Neurogenetics
Ajroud-Driss, Senda S; Fecto, Faisal F; Ajroud, Kaouther K; Lalani, Irfan I; Calvo, Sarah E SE; Mootha, Vamsi K VK; Deng, Han-Xiang HX; Siddique, Nailah N; Tahmoush, Albert J AJ; Heiman-Patterson, Terry D TD; Siddique, Teepu T
Publication Date: 2015-01

Variant appearance in text: rs2283792
PubMed Link: 25193783
Variant Present in the following documents:
  • Main text
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No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis.

Human Molecular Genetics
Goris, An A; van Setten, Jessica J; Diekstra, Frank F; Ripke, Stephan S; Patsopoulos, Nikolaos A NA; Sawcer, Stephen J SJ; , ; van Es, Michael M; , ; Andersen, Peter M PM; Melki, Judith J; Meininger, Vincent V; Hardiman, Orla O; Landers, John E JE; Brown, Robert H RH; Shatunov, Aleksey A; Leigh, Nigel N; Al-Chalabi, Ammar A; Shaw, Christopher E CE; Traynor, Bryan J BJ; Chiò, Adriano A; Restagno, Gabriella G; Mora, Gabriele G; Ophoff, Roel A RA; Oksenberg, Jorge R JR; Van Damme, Philip P; Compston, Alastair A; Robberecht, Wim W; Dubois, Bénédicte B; van den Berg, Leonard H LH; De Jager, Philip L PL; Veldink, Jan H JH; de Bakker, Paul I W PI
Publication Date: 2014-04-01

Variant appearance in text: rs2283792
PubMed Link: 24234648
Variant Present in the following documents:
  • Main text
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Discovery and functional assessment of gene variants in the vascular endothelial growth factor pathway.

Human Mutation
Paré-Brunet, Laia L; Glubb, Dylan D; Evans, Patrick P; Berenguer-Llergo, Antoni A; Etheridge, Amy S AS; Skol, Andrew D AD; Di Rienzo, Anna A; Duan, Shiwei S; Gamazon, Eric R ER; Innocenti, Federico F
Publication Date: 2014-02

Variant appearance in text: rs2283792
PubMed Link: 24186849
Variant Present in the following documents:
  • Main text
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Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.

Nature Genetics
, ; Beecham, Ashley H AH; Patsopoulos, Nikolaos A NA; Xifara, Dionysia K DK; Davis, Mary F MF; Kemppinen, Anu A; Cotsapas, Chris C; Shah, Tejas S TS; Spencer, Chris C; Booth, David D; Goris, An A; Oturai, Annette A; Saarela, Janna J; Fontaine, Bertrand B; Hemmer, Bernhard B; Martin, Claes C; Zipp, Frauke F; D'Alfonso, Sandra S; Martinelli-Boneschi, Filippo F; Taylor, Bruce B; Harbo, Hanne F HF; Kockum, Ingrid I; Hillert, Jan J; Olsson, Tomas T; Ban, Maria M; Oksenberg, Jorge R JR; Hintzen, Rogier R; Barcellos, Lisa F LF; , ; , ; Agliardi, Cristina C; Alfredsson, Lars L; Alizadeh, Mehdi M; Anderson, Carl C; Andrews, Robert R; Søndergaard, Helle Bach HB; Baker, Amie A; Band, Gavin G; Baranzini, Sergio E SE; Barizzone, Nadia N; Barrett, Jeffrey J; Bellenguez, Céline C; Bergamaschi, Laura L; Bernardinelli, Luisa L; Berthele, Achim A; Biberacher, Viola V; Binder, Thomas M C TM; Blackburn, Hannah H; Bomfim, Izaura L IL; Brambilla, Paola P; Broadley, Simon S; Brochet, Bruno B; Brundin, Lou L; Buck, Dorothea D; Butzkueven, Helmut H; Caillier, Stacy J SJ; Camu, William W; Carpentier, Wassila W; Cavalla, Paola P; Celius, Elisabeth G EG; Coman, Irène I; Comi, Giancarlo G; Corrado, Lucia L; Cosemans, Leentje L; Cournu-Rebeix, Isabelle I; Cree, Bruce A C BA; Cusi, Daniele D; Damotte, Vincent V; Defer, Gilles G; Delgado, Silvia R SR; Deloukas, Panos P; di Sapio, Alessia A; Dilthey, Alexander T AT; Donnelly, Peter P; Dubois, Bénédicte B; Duddy, Martin M; Edkins, Sarah S; Elovaara, Irina I; Esposito, Federica F; Evangelou, Nikos N; Fiddes, Barnaby B; Field, Judith J; Franke, Andre A; Freeman, Colin C; Frohlich, Irene Y IY; Galimberti, Daniela D; Gieger, Christian C; Gourraud, Pierre-Antoine PA; Graetz, Christiane C; Graham, Andrew A; Grummel, Verena V; Guaschino, Clara C; Hadjixenofontos, Athena A; Hakonarson, Hakon H; Halfpenny, Christopher C; Hall, Gillian G; Hall, Per P; Hamsten, Anders A; Harley, James J; Harrower, Timothy T; Hawkins, Clive C; Hellenthal, Garrett G; Hillier, Charles C; Hobart, Jeremy J; Hoshi, Muni M; Hunt, Sarah E SE; Jagodic, Maja M; Jelčić, Ilijas I; Jochim, Angela A; Kendall, Brian B; Kermode, Allan A; Kilpatrick, Trevor T; Koivisto, Keijo K; Konidari, Ioanna I; Korn, Thomas T; Kronsbein, Helena H; Langford, Cordelia C; Larsson, Malin M; Lathrop, Mark M; Lebrun-Frenay, Christine C; Lechner-Scott, Jeannette J; Lee, Michelle H MH; Leone, Maurizio A MA; Leppä, Virpi V; Liberatore, Giuseppe G; Lie, Benedicte A BA; Lill, Christina M CM; Lindén, Magdalena M; Link, Jenny J; Luessi, Felix F; Lycke, Jan J; Macciardi, Fabio F; Männistö, Satu S; Manrique, Clara P CP; Martin, Roland R; Martinelli, Vittorio V; Mason, Deborah D; Mazibrada, Gordon G; McCabe, Cristin C; Mero, Inger-Lise IL; Mescheriakova, Julia J; Moutsianas, Loukas L; Myhr, Kjell-Morten KM; Nagels, Guy G; Nicholas, Richard R; Nilsson, Petra P; Piehl, Fredrik F; Pirinen, Matti M; Price, Siân E SE; Quach, Hong H; Reunanen, Mauri M; Robberecht, Wim W; Robertson, Neil P NP; Rodegher, Mariaemma M; Rog, David D; Salvetti, Marco M; Schnetz-Boutaud, Nathalie C NC; Sellebjerg, Finn F; Selter, Rebecca C RC; Schaefer, Catherine C; Shaunak, Sandip S; Shen, Ling L; Shields, Simon S; Siffrin, Volker V; Slee, Mark M; Sorensen, Per Soelberg PS; Sorosina, Melissa M; Sospedra, Mireia M; Spurkland, Anne A; Strange, Amy A; Sundqvist, Emilie E; Thijs, Vincent V; Thorpe, John J; Ticca, Anna A; Tienari, Pentti P; van Duijn, Cornelia C; Visser, Elizabeth M EM; Vucic, Steve S; Westerlind, Helga H; Wiley, James S JS; Wilkins, Alastair A; Wilson, James F JF; Winkelmann, Juliane J; Zajicek, John J; Zindler, Eva E; Haines, Jonathan L JL; Pericak-Vance, Margaret A MA; Ivinson, Adrian J AJ; Stewart, Graeme G; Hafler, David D; Hauser, Stephen L SL; Compston, Alastair A; McVean, Gil G; De Jager, Philip P; Sawcer, Stephen J SJ; McCauley, Jacob L JL
Publication Date: 2013-11

Variant appearance in text: rs2283792
PubMed Link: 24076602
Variant Present in the following documents:
  • Main text
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The genetics of multiple sclerosis: review of current and emerging candidates.

The Application Of Clinical Genetics
Muñoz-Culla, Maider M; Irizar, Haritz H; Otaegui, David D
Publication Date: 2013

Variant appearance in text: rs2283792
PubMed Link: 24019748
Variant Present in the following documents:
  • Main text
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A Novel Stratification Method in Linkage Studies to Address Inter- and Intra-Family Heterogeneity in Autism.

Plos One
Talebizadeh, Zohreh Z; Arking, Dan E DE; Hu, Valerie W VW
Publication Date: 2013

Variant appearance in text: rs2283792
PubMed Link: 23840741
Variant Present in the following documents:
  • Main text
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Progress in multiple sclerosis genetics.

Current Genomics
Goris, An A; Pauwels, Ine I; Dubois, Bénédicte B
Publication Date: 2012-12

Variant appearance in text: rs2283792
PubMed Link: 23730204
Variant Present in the following documents:
  • Main text
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Protein-protein interaction analysis highlights additional loci of interest for multiple sclerosis.

Plos One
Ragnedda, Giammario G; Disanto, Giulio G; Giovannoni, Gavin G; Ebers, George C GC; Sotgiu, Stefano S; Ramagopalan, Sreeram V SV
Publication Date: 2012

Variant appearance in text: rs2283792
PubMed Link: 23094030
Variant Present in the following documents:
  • Main text
  • pone.0046730.pdf
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The genetics of multiple sclerosis: an up-to-date review.

Immunological Reviews
Gourraud, Pierre-Antoine PA; Harbo, Hanne F HF; Hauser, Stephen L SL; Baranzini, Sergio E SE
Publication Date: 2012-07

Variant appearance in text: rs2283792
PubMed Link: 22725956
Variant Present in the following documents:
  • Main text
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Genomic regions associated with multiple sclerosis are active in B cells.

Plos One
Disanto, Giulio G; Sandve, Geir Kjetil GK; Berlanga-Taylor, Antonio J AJ; Morahan, Julia M JM; Dobson, Ruth R; Giovannoni, Gavin G; Ramagopalan, Sreeram V SV
Publication Date: 2012

Variant appearance in text: rs2283792
PubMed Link: 22396755
Variant Present in the following documents:
  • Main text
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Perspectives on the use of multiple sclerosis risk genes for prediction.

Plos One
Jafari, Naghmeh N; Broer, Linda L; van Duijn, Cornelia M CM; Janssens, A Cecile J W AC; Hintzen, Rogier Q RQ
Publication Date: 2011

Variant appearance in text: rs2283792
PubMed Link: 22164203
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.

Nature
, ; , ; Sawcer, Stephen S; Hellenthal, Garrett G; Pirinen, Matti M; Spencer, Chris C A CC; Patsopoulos, Nikolaos A NA; Moutsianas, Loukas L; Dilthey, Alexander A; Su, Zhan Z; Freeman, Colin C; Hunt, Sarah E SE; Edkins, Sarah S; Gray, Emma E; Booth, David R DR; Potter, Simon C SC; Goris, An A; Band, Gavin G; Oturai, Annette Bang AB; Strange, Amy A; Saarela, Janna J; Bellenguez, Céline C; Fontaine, Bertrand B; Gillman, Matthew M; Hemmer, Bernhard B; Gwilliam, Rhian R; Zipp, Frauke F; Jayakumar, Alagurevathi A; Martin, Roland R; Leslie, Stephen S; Hawkins, Stanley S; Giannoulatou, Eleni E; D'alfonso, Sandra S; Blackburn, Hannah H; Martinelli Boneschi, Filippo F; Liddle, Jennifer J; Harbo, Hanne F HF; Perez, Marc L ML; Spurkland, Anne A; Waller, Matthew J MJ; Mycko, Marcin P MP; Ricketts, Michelle M; Comabella, Manuel M; Hammond, Naomi N; Kockum, Ingrid I; McCann, Owen T OT; Ban, Maria M; Whittaker, Pamela P; Kemppinen, Anu A; Weston, Paul P; Hawkins, Clive C; Widaa, Sara S; Zajicek, John J; Dronov, Serge S; Robertson, Neil N; Bumpstead, Suzannah J SJ; Barcellos, Lisa F LF; Ravindrarajah, Rathi R; Abraham, Roby R; Alfredsson, Lars L; Ardlie, Kristin K; Aubin, Cristin C; Baker, Amie A; Baker, Katharine K; Baranzini, Sergio E SE; Bergamaschi, Laura L; Bergamaschi, Roberto R; Bernstein, Allan A; Berthele, Achim A; Boggild, Mike M; Bradfield, Jonathan P JP; Brassat, David D; Broadley, Simon A SA; Buck, Dorothea D; Butzkueven, Helmut H; Capra, Ruggero R; Carroll, William M WM; Cavalla, Paola P; Celius, Elisabeth G EG; Cepok, Sabine S; Chiavacci, Rosetta R; Clerget-Darpoux, Françoise F; Clysters, Katleen K; Comi, Giancarlo G; Cossburn, Mark M; Cournu-Rebeix, Isabelle I; Cox, Mathew B MB; Cozen, Wendy W; Cree, Bruce A C BA; Cross, Anne H AH; Cusi, Daniele D; Daly, Mark J MJ; Davis, Emma E; de Bakker, Paul I W PI; Debouverie, Marc M; D'hooghe, Marie Beatrice MB; Dixon, Katherine K; Dobosi, Rita R; Dubois, Bénédicte B; Ellinghaus, David D; Elovaara, Irina I; Esposito, Federica F; Fontenille, Claire C; Foote, Simon S; Franke, Andre A; Galimberti, Daniela D; Ghezzi, Angelo A; Glessner, Joseph J; Gomez, Refujia R; Gout, Olivier O; Graham, Colin C; Grant, Struan F A SF; Guerini, Franca Rosa FR; Hakonarson, Hakon H; Hall, Per P; Hamsten, Anders A; Hartung, Hans-Peter HP; Heard, Rob N RN; Heath, Simon S; Hobart, Jeremy J; Hoshi, Muna M; Infante-Duarte, Carmen C; Ingram, Gillian G; Ingram, Wendy W; Islam, Talat T; Jagodic, Maja M; Kabesch, Michael M; Kermode, Allan G AG; Kilpatrick, Trevor J TJ; Kim, Cecilia C; Klopp, Norman N; Koivisto, Keijo K; Larsson, Malin M; Lathrop, Mark M; Lechner-Scott, Jeannette S JS; Leone, Maurizio A MA; Leppä, Virpi V; Liljedahl, Ulrika U; Bomfim, Izaura Lima IL; Lincoln, Robin R RR; Link, Jenny J; Liu, Jianjun J; Lorentzen, Aslaug R AR; Lupoli, Sara S; Macciardi, Fabio F; Mack, Thomas T; Marriott, Mark M; Martinelli, Vittorio V; Mason, Deborah D; McCauley, Jacob L JL; Mentch, Frank F; Mero, Inger-Lise IL; Mihalova, Tania T; Montalban, Xavier X; Mottershead, John J; Myhr, Kjell-Morten KM; Naldi, Paola P; Ollier, William W; Page, Alison A; Palotie, Aarno A; Pelletier, Jean J; Piccio, Laura L; Pickersgill, Trevor T; Piehl, Fredrik F; Pobywajlo, Susan S; Quach, Hong L HL; Ramsay, Patricia P PP; Reunanen, Mauri M; Reynolds, Richard R; Rioux, John D JD; Rodegher, Mariaemma M; Roesner, Sabine S; Rubio, Justin P JP; Rückert, Ina-Maria IM; Salvetti, Marco M; Salvi, Erika E; Santaniello, Adam A; Schaefer, Catherine A CA; Schreiber, Stefan S; Schulze, Christian C; Scott, Rodney J RJ; Sellebjerg, Finn F; Selmaj, Krzysztof W KW; Sexton, David D; Shen, Ling L; Simms-Acuna, Brigid B; Skidmore, Sheila S; Sleiman, Patrick M A PM; Smestad, Cathrine C; Sørensen, Per Soelberg PS; Søndergaard, Helle Bach HB; Stankovich, Jim J; Strange, Richard C RC; Sulonen, Anna-Maija AM; Sundqvist, Emilie E; Syvänen, Ann-Christine AC; Taddeo, Francesca F; Taylor, Bruce B; Blackwell, Jenefer M JM; Tienari, Pentti P; Bramon, Elvira E; Tourbah, Ayman A; Brown, Matthew A MA; Tronczynska, Ewa E; Casas, Juan P JP; Tubridy, Niall N; Corvin, Aiden A; Vickery, Jane J; Jankowski, Janusz J; Villoslada, Pablo P; Markus, Hugh S HS; Wang, Kai K; Mathew, Christopher G CG; Wason, James J; Palmer, Colin N A CN; Wichmann, H-Erich HE; Plomin, Robert R; Willoughby, Ernest E; Rautanen, Anna A; Winkelmann, Juliane J; Wittig, Michael M; Trembath, Richard C RC; Yaouanq, Jacqueline J; Viswanathan, Ananth C AC; Zhang, Haitao H; Wood, Nicholas W NW; Zuvich, Rebecca R; Deloukas, Panos P; Langford, Cordelia C; Duncanson, Audrey A; Oksenberg, Jorge R JR; Pericak-Vance, Margaret A MA; Haines, Jonathan L JL; Olsson, Tomas T; Hillert, Jan J; Ivinson, Adrian J AJ; De Jager, Philip L PL; Peltonen, Leena L; Stewart, Graeme J GJ; Hafler, David A DA; Hauser, Stephen L SL; McVean, Gil G; Donnelly, Peter P; Compston, Alastair A
Publication Date: 2011-08-10

Variant appearance in text: rs2283792
PubMed Link: 21833088
Variant Present in the following documents:
  • NIHMS36028-supplement-1.pdf
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Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.

American Journal Of Human Genetics
Melquist, Stacey S; Craig, David W DW; Huentelman, Matthew J MJ; Crook, Richard R; Pearson, John V JV; Baker, Matt M; Zismann, Victoria L VL; Gass, Jennifer J; Adamson, Jennifer J; Szelinger, Szabolcs S; Corneveaux, Jason J; Cannon, Ashley A; Coon, Keith D KD; Lincoln, Sarah S; Adler, Charles C; Tuite, Paul P; Calne, Donald B DB; Bigio, Eileen H EH; Uitti, Ryan J RJ; Wszolek, Zbigniew K ZK; Golbe, Lawrence I LI; Caselli, Richard J RJ; Graff-Radford, Neill N; Litvan, Irene I; Farrer, Matthew J MJ; Dickson, Dennis W DW; Hutton, Mike M; Stephan, Dietrich A DA
Publication Date: 2007-04

Variant appearance in text: rs2283792
PubMed Link: 17357082
Variant Present in the following documents:
  • Main text
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