Publications:

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Genome-wide association studies reveal shared genetic haplotypes of autoimmune rheumatic and endocrine diseases with psychiatric disorders.

Brain And Behavior

Voskarides, Konstantinos K; Giannopoulou, Nefeli N; Eid, Rasha R; Parperis, Konstantinos K; Chatzittofis, Andreas A

Publication Date: 2023-03-16

Variant appearance in text: rs4625

PubMed Link: 36924079

Variant Present in the following documents:

• Main text
• BRB3-13-e2955.pdf

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Thirteen Independent Genetic Loci Associated with Preserved Processing Speed in a Study of Cognitive Resilience in 330,097 Individuals in the UK Biobank.

Genes

Fitzgerald, Joan J; Fahey, Laura L; Holleran, Laurena L; Ó Broin, Pilib P; Donohoe, Gary G; Morris, Derek W DW

Publication Date: 2022-01-10

Variant appearance in text: rs4625

PubMed Link: 35052462

Variant Present in the following documents:

• Main text
• genes-13-00122.pdf

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Thirteen Independent Genetic Loci Associated with Preserved Processing Speed in a Study of Cognitive Resilience in 330,097 Individuals in the UK Biobank.

Genes

Fitzgerald, Joan J; Fahey, Laura L; Holleran, Laurena L; Ó Broin, Pilib P; Donohoe, Gary G; Morris, Derek W DW

Publication Date: 2022-01-10

Variant appearance in text: rs4625

PubMed Link: 35052462

Variant Present in the following documents:

• Main text
• genes-13-00122.pdf

View BVdb publication page

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Genetic analysis of sinonasal undifferentiated carcinoma discovers recurrent SWI/SNF alterations and a novel PGAP3-SRPK1 fusion gene.

Bmc Cancer

Heft Neal, Molly E ME; Birkeland, Andrew C AC; Bhangale, Apurva D AD; Zhai, Jingyi J; Kulkarni, Aditi A; Foltin, Susan K SK; Jewell, Brittany M BM; Ludwig, Megan L ML; Pinatti, Lisa L; Jiang, Hui H; McHugh, Jonathan B JB; Marentette, Lawence L; McKean, Erin L EL; Brenner, J Chad JC

Publication Date: 2021-05-29

Variant appearance in text: rs4625

PubMed Link: 34051734

Variant Present in the following documents:

• 12885_2021_8370_MOESM15_ESM.xlsx, sheet 1

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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: rs4625

PubMed Link: 32879140

Variant Present in the following documents:

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

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Item-level analyses reveal genetic heterogeneity in neuroticism.

Nature Communications

Nagel, Mats M; Watanabe, Kyoko K; Stringer, Sven S; Posthuma, Danielle D; van der Sluis, Sophie S

Publication Date: 2018-03-02

Variant appearance in text: rs4625

PubMed Link: 29500382

Variant Present in the following documents:

• 41467_2018_3242_MOESM2_ESM.pdf

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Signatures of Evolutionary Adaptation in Quantitative Trait Loci Influencing Trace Element Homeostasis in Liver.

Molecular Biology And Evolution

Engelken, Johannes J; Espadas, Guadalupe G; Mancuso, Francesco M FM; Bonet, Nuria N; Scherr, Anna-Lena AL; Jímenez-Álvarez, Victoria V; Codina-Solà, Marta M; Medina-Stacey, Daniel D; Spataro, Nino N; Stoneking, Mark M; Calafell, Francesc F; Sabidó, Eduard E; Bosch, Elena E

Publication Date: 2016-03

Variant appearance in text: rs4625

PubMed Link: 26582562

Variant Present in the following documents:

• Main text
• msv267.pdf

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Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases.

Nature Medicine

Li, Yun R YR; Li, Jin J; Zhao, Sihai D SD; Bradfield, Jonathan P JP; Mentch, Frank D FD; Maggadottir, S Melkorka SM; Hou, Cuiping C; Abrams, Debra J DJ; Chang, Diana D; Gao, Feng F; Guo, Yiran Y; Wei, Zhi Z; Connolly, John J JJ; Cardinale, Christopher J CJ; Bakay, Marina M; Glessner, Joseph T JT; Li, Dong D; Kao, Charlly C; Thomas, Kelly A KA; Qiu, Haijun H; Chiavacci, Rosetta M RM; Kim, Cecilia E CE; Wang, Fengxiang F; Snyder, James J; Richie, Marylyn D MD; Flatø, Berit B; Førre, Øystein Ø; Denson, Lee A LA; Thompson, Susan D SD; Becker, Mara L ML; Guthery, Stephen L SL; Latiano, Anna A; Perez, Elena E; Resnick, Elena E; Russell, Richard K RK; Wilson, David C DC; Silverberg, Mark S MS; Annese, Vito V; Lie, Benedicte A BA; Punaro, Marilynn M; Dubinsky, Marla C MC; Monos, Dimitri S DS; Strisciuglio, Caterina C; Staiano, Annamaria A; Miele, Erasmo E; Kugathasan, Subra S; Ellis, Justine A JA; Munro, Jane E JE; Sullivan, Kathleen E KE; Wise, Carol A CA; Chapel, Helen H; Cunningham-Rundles, Charlotte C; Grant, Struan F A SF; Orange, Jordan S JS; Sleiman, Patrick M A PM; Behrens, Edward M EM; Griffiths, Anne M AM; Satsangi, Jack J; Finkel, Terri H TH; Keinan, Alon A; Prak, Eline T Luning ET; Polychronakos, Constantin C; Baldassano, Robert N RN; Li, Hongzhe H; Keating, Brendan J BJ; Hakonarson, Hakon H

Publication Date: 2015-09

Variant appearance in text: rs4625

PubMed Link: 26301688

Variant Present in the following documents:

• Main text

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Proteogenomic analysis reveals exosomes are more oncogenic than ectosomes.

Oncotarget

Keerthikumar, Shivakumar S; Gangoda, Lahiru L; Liem, Michael M; Fonseka, Pamali P; Atukorala, Ishara I; Ozcitti, Cemil C; Mechler, Adam A; Adda, Christopher G CG; Ang, Ching-Seng CS; Mathivanan, Suresh S

Publication Date: 2015-06-20

Variant appearance in text: rs4625

PubMed Link: 25944692

Variant Present in the following documents:

• oncotarget-06-15375-s005.xlsx, sheet 2

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Pancreatic islet enhancer clusters enriched in type 2 diabetes risk-associated variants.

Nature Genetics

Pasquali, Lorenzo L; Gaulton, Kyle J KJ; Rodríguez-Seguí, Santiago A SA; Mularoni, Loris L; Miguel-Escalada, Irene I; Akerman, İldem İ; Tena, Juan J JJ; Morán, Ignasi I; Gómez-Marín, Carlos C; van de Bunt, Martijn M; Ponsa-Cobas, Joan J; Castro, Natalia N; Nammo, Takao T; Cebola, Inês I; García-Hurtado, Javier J; Maestro, Miguel Angel MA; Pattou, François F; Piemonti, Lorenzo L; Berney, Thierry T; Gloyn, Anna L AL; Ravassard, Philippe P; Skarmeta, José Luis Gómez JLG; Müller, Ferenc F; McCarthy, Mark I MI; Ferrer, Jorge J

Publication Date: 2014-02

Variant appearance in text: rs4625

PubMed Link: 24413736

Variant Present in the following documents:

• NIHMS56019-supplement-1.pdf

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Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.

Human Molecular Genetics

McGovern, Dermot P B DP; Jones, Michelle R MR; Taylor, Kent D KD; Marciante, Kristin K; Yan, Xiaofei X; Dubinsky, Marla M; Ippoliti, Andy A; Vasiliauskas, Eric E; Berel, Dror D; Derkowski, Carrie C; Dutridge, Deb D; Fleshner, Phil P; Shih, David Q DQ; Melmed, Gil G; Mengesha, Emebet E; King, Lily L; Pressman, Sheila S; Haritunians, Talin T; Guo, Xiuqing X; Targan, Stephan R SR; Rotter, Jerome I JI; ,

Publication Date: 2010-09-01

Variant appearance in text: rs4625

PubMed Link: 20570966

Variant Present in the following documents:

• Main text

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