Publications:

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Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels.

Communications Biology

Sarnowski, Chloé C; Ghanbari, Mohsen M; Bis, Joshua C JC; Logue, Mark M; Fornage, Myriam M; Mishra, Aniket A; Ahmad, Shahzad S; Beiser, Alexa S AS; Boerwinkle, Eric E; Bouteloup, Vincent V; Chouraki, Vincent V; Cupples, L Adrienne LA; Damotte, Vincent V; DeCarli, Charles S CS; DeStefano, Anita L AL; Djoussé, Luc L; Fohner, Alison E AE; Franz, Carol E CE; Kautz, Tiffany F TF; Lambert, Jean-Charles JC; Lyons, Michael J MJ; Mosley, Thomas H TH; Mukamal, Kenneth J KJ; Pase, Matthew P MP; Portilla Fernandez, Eliana C EC; Rissman, Robert A RA; Satizabal, Claudia L CL; Vasan, Ramachandran S RS; Yaqub, Amber A; Debette, Stephanie S; Dufouil, Carole C; Launer, Lenore J LJ; Kremen, William S WS; Longstreth, William T WT; Ikram, M Arfan MA; Seshadri, Sudha S

Publication Date: 2022-04-08

Variant appearance in text: rs8072451

PubMed Link: 35396452

Variant Present in the following documents:

• Main text
• 42003_2022_Article_3287.pdf

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Association and Genetic Expression between Genes Involved in HPA Axis and Suicide Behavior: A Systematic Review.

Genes

Hernández-Díaz, Yazmín Y; Genis-Mendoza, Alma Delia AD; González-Castro, Thelma Beatriz TB; Tovilla-Zárate, Carlos Alfonso CA; Juárez-Rojop, Isela Esther IE; López-Narváez, María Lilia ML; Nicolini, Humberto H

Publication Date: 2021-10-13

Variant appearance in text: rs8072451

PubMed Link: 34681002

Variant Present in the following documents:

• Main text
• genes-12-01608.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: rs8072451

PubMed Link: 32879140

Variant Present in the following documents:

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

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Further evidence for the association of GAL, GALR1 and NPY1R variants with opioid dependence.

Pharmacogenomics

Randesi, Matthew M; Levran, Orna O; den Brink, Wim van WV; Blanken, Peter P; van Ree, Jan M JM; Ott, Jurg J; Kreek, Mary J MJ

Publication Date: 2020-08

Variant appearance in text: rs8072451

PubMed Link: 32757697

Variant Present in the following documents:

• Main text

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Chromatin interactions and expression quantitative trait loci reveal genetic drivers of multimorbidities.

Nature Communications

Fadason, Tayaza T; Schierding, William W; Lumley, Thomas T; O'Sullivan, Justin M JM

Publication Date: 2018-12-05

Variant appearance in text: rs8072451

PubMed Link: 30518762

Variant Present in the following documents:

• Main text
• 41467_2018_Article_7692.pdf

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To ERV Is Human: A Phenotype-Wide Scan Linking Polymorphic Human Endogenous Retrovirus-K Insertions to Complex Phenotypes.

Frontiers In Genetics

Wallace, Amelia D AD; Wendt, George A GA; Barcellos, Lisa F LF; de Smith, Adam J AJ; Walsh, Kyle M KM; Metayer, Catherine C; Costello, Joseph F JF; Wiemels, Joseph L JL; Francis, Stephen S SS

Publication Date: 2018

Variant appearance in text: rs8072451

PubMed Link: 30154825

Variant Present in the following documents:

• Main text
• fgene-09-00298.pdf

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Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases.

Jama Neurology

Witoelar, Aree A; Jansen, Iris E IE; Wang, Yunpeng Y; Desikan, Rahul S RS; Gibbs, J Raphael JR; Blauwendraat, Cornelis C; Thompson, Wesley K WK; Hernandez, Dena G DG; Djurovic, Srdjan S; Schork, Andrew J AJ; Bettella, Francesco F; Ellinghaus, David D; Franke, Andre A; Lie, Benedicte A BA; McEvoy, Linda K LK; Karlsen, Tom H TH; Lesage, Suzanne S; Morris, Huw R HR; Brice, Alexis A; Wood, Nicholas W NW; Heutink, Peter P; Hardy, John J; Singleton, Andrew B AB; Dale, Anders M AM; Gasser, Thomas T; Andreassen, Ole A OA; Sharma, Manu M; ,

Publication Date: 2017-07-01

Variant appearance in text: rs8072451

PubMed Link: 28586827

Variant Present in the following documents:

• Main text

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Association of Variants of Arginine Vasopressin and Arginine Vasopressin Receptor 1A With Severe Acetaminophen Liver Injury.

Cellular And Molecular Gastroenterology And Hepatology

Randesi, Matthew M; Levran, Orna O; Correa da Rosa, Joel J; Hankins, Julia J; Rule, Jody J; Kreek, Mary Jeanne MJ; Lee, William M WM; ,

Publication Date: 2017-05

Variant appearance in text: rs8072451

PubMed Link: 28462386

Variant Present in the following documents:

• Main text
• main.pdf

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Effects of GWAS-associated genetic variants on lncRNAs within IBD and T1D candidate loci.

Plos One

Mirza, Aashiq H AH; Kaur, Simranjeet S; Brorsson, Caroline A CA; Pociot, Flemming F

Publication Date: 2014

Variant appearance in text: rs8072451

PubMed Link: 25144376

Variant Present in the following documents:

• pone.0105723.s013.xlsx, sheet 2

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Drug addiction and stress-response genetic variability: association study in African Americans.

Annals Of Human Genetics

Levran, Orna O; Randesi, Matthew M; Li, Yi Y; Rotrosen, John J; Ott, Jurg J; Adelson, Miriam M; Kreek, Mary Jeanne MJ

Publication Date: 2014-07

Variant appearance in text: rs8072451

PubMed Link: 24766650

Variant Present in the following documents:

• Main text

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Two HPA axis genes, CRHBP and FKBP5, interact with childhood trauma to increase the risk for suicidal behavior.

Journal Of Psychiatric Research

Roy, Alec A; Hodgkinson, Colin A CA; Deluca, Vincenzo V; Goldman, David D; Enoch, Mary-Anne MA

Publication Date: 2012-01

Variant appearance in text: rs8072451

PubMed Link: 21978546

Variant Present in the following documents:

• Main text

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Linkage disequilibrium and association of MAPT H1 in Parkinson disease.

American Journal Of Human Genetics

Skipper, Lisa L; Wilkes, Kristen K; Toft, Mathias M; Baker, Matthew M; Lincoln, Sarah S; Hulihan, Mary M; Ross, Owen A OA; Hutton, Mike M; Aasly, Jan J; Farrer, Matthew M

Publication Date: 2004-10

Variant appearance in text: rs8072451

PubMed Link: 15297935

Variant Present in the following documents:

• Main text

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