Publications:

The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism.

Nature Communications

Xia, Charley C; Pickett, Sarah J SJ; Liewald, David C M DCM; Weiss, Alexander A; Hudson, Gavin G; Hill, W David WD

Publication Date: 2023-05-30

Variant appearance in text: rs113434679

PubMed Link: 37253732

Variant Present in the following documents:

• Main text
• 41467_2023_Article_38480.pdf

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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: rs113434679

PubMed Link: 36337698

Variant Present in the following documents:

• Main text
• fnagi-14-1021918.pdf

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GWAS of stool frequency provides insights into gastrointestinal motility and irritable bowel syndrome.

Cell Genomics

Bonfiglio, Ferdinando F; Liu, Xingrong X; Smillie, Christopher C; Pandit, Anita A; Kurilshikov, Alexander A; Bacigalupe, Rodrigo R; Zheng, Tenghao T; Nim, Hieu H; Garcia-Etxebarria, Koldo K; Bujanda, Luis L; Andreasson, Anna A; Agreus, Lars L; Walter, Susanna S; Abecasis, Gonçalo G; Eijsbouts, Chris C; Jostins, Luke L; Parkes, Miles M; Hughes, David A DA; Timpson, Nicholas N; Raes, Jeroen J; Franke, Andre A; Kennedy, Nicholas A NA; Regev, Aviv A; Zhernakova, Alexandra A; Simren, Magnus M; Camilleri, Michael M; D'Amato, Mauro M

Publication Date: 2021-12-08

Variant appearance in text: rs113434679

PubMed Link: 34957435

Variant Present in the following documents:

• mmc2.pdf
• mmc1.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: rs113434679

PubMed Link: 32879140

Variant Present in the following documents:

• jciinsight-5-136477-s105.xlsx, sheet 5

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The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight.

Movement Disorders : Official Journal Of The Movement Disorder Society

Bandres-Ciga, Sara S; Ahmed, Sarah S; Sabir, Marya S MS; Blauwendraat, Cornelis C; Adarmes-Gómez, Astrid D AD; Bernal-Bernal, Inmaculada I; Bonilla-Toribio, Marta M; Buiza-Rueda, Dolores D; Carrillo, Fátima F; Carrión-Claro, Mario M; Gómez-Garre, Pilar P; Jesús, Silvia S; Labrador-Espinosa, Miguel A MA; Macias, Daniel D; Méndez-Del-Barrio, Carlota C; Periñán-Tocino, Teresa T; Tejera-Parrado, Cristina C; Vargas-González, Laura L; Diez-Fairen, Monica M; Alvarez, Ignacio I; Tartari, Juan Pablo JP; Buongiorno, Mariateresa M; Aguilar, Miquel M; Gorostidi, Ana A; Bergareche, Jesús Alberto JA; Mondragon, Elisabet E; Vinagre-Aragon, Ana A; Croitoru, Ioana I; Ruiz-Martínez, Javier J; Dols-Icardo, Oriol O; Kulisevsky, Jaime J; Marín-Lahoz, Juan J; Pagonabarraga, Javier J; Pascual-Sedano, Berta B; Ezquerra, Mario M; Cámara, Ana A; Compta, Yaroslau Y; Fernández, Manel M; Fernández-Santiago, Rubén R; Muñoz, Esteban E; Tolosa, Eduard E; Valldeoriola, Francesc F; Gonzalez-Aramburu, Isabel I; Sanchez Rodriguez, Antonio A; Sierra, María M; Menéndez-González, Manuel M; Blazquez, Marta M; Garcia, Ciara C; Suarez-San Martin, Esther E; García-Ruiz, Pedro P; Martínez-Castrillo, Juan Carlos JC; Vela-Desojo, Lydia L; Ruz, Clara C; Barrero, Francisco Javier FJ; Escamilla-Sevilla, Francisco F; Mínguez-Castellanos, Adolfo A; Cerdan, Debora D; Tabernero, Cesar C; Gomez Heredia, Maria Jose MJ; Perez Errazquin, Francisco F; Romero-Acebal, Manolo M; Feliz, Cici C; Lopez-Sendon, Jose Luis JL; Mata, Marina M; Martínez Torres, Irene I; Kim, Jonggeol Jeffrey JJ; Dalgard, Clifton L CL; , ; Brooks, Janet J; Saez-Atienzar, Sara S; Gibbs, J Raphael JR; Jorda, Rafael R; Botia, Juan A JA; Bonet-Ponce, Luis L; Morrison, Karen E KE; Clarke, Carl C; Tan, Manuela M; Morris, Huw H; Edsall, Connor C; Hernandez, Dena D; Simon-Sanchez, Javier J; Nalls, Mike A MA; Scholz, Sonja W SW; Jimenez-Escrig, Adriano A; Duarte, Jacinto J; Vives, Francisco F; Duran, Raquel R; Hoenicka, Janet J; Alvarez, Victoria V; Infante, Jon J; Marti, Maria José MJ; Clarimón, Jordi J; López de Munain, Adolfo A; Pastor, Pau P; Mir, Pablo P; Singleton, Andrew A; ,

Publication Date: 2019-12

Variant appearance in text: rs113434679

PubMed Link: 31660654

Variant Present in the following documents:

• Main text

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