Imaging-Genetics in Dyslexia: Connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments

by Eicher, John D., Gruen, Jeffrey R.
Published 2013

Language impairment and dyslexia genes influence language skills in children with autism spectrum disorders

by Eicher, John D., Gruen, Jeffrey R.
Published in Autism Res (2014)

The genetics of platelet count and volume in humans

by Eicher, John D., Lettre, Guillaume, Johnson, Andrew D.
Published in Platelets (2017)

Replication and hematological characterization of human platelet reactivity genetic associations in men from the Caerphilly Prospective Study (CaPS)

by Eicher, John D., Xue, Luting, Ben-Shlomo, Yoav, Beswick, Andrew D., Johnson, Andrew D.
Published in J Thromb Thrombolysis (2016)

Alleles of a Polymorphic ETV6 Binding Site in DCDC2 Confer Risk of Reading and Language Impairment

by Powers, Natalie R., Eicher, John D., Butter, Falk, Kong, Yong, Miller, Laura L., Ring, Susan M., Mann, Matthias, Gruen, Jeffrey R.
Published 2013

Alleles of a Polymorphic ETV6 Binding Site in DCDC2 Confer Risk of Reading and Language Impairment

by Powers, Natalie R., Eicher, John D., Butter, Falk, Kong, Yong, Miller, Laura L., Ring, Susan M., Mann, Matthias, Gruen, Jeffrey R.
Published 2014

GRASP v2.0: an update on the Genome-Wide Repository of Associations between SNPs and phenotypes

by Eicher, John D., Landowski, Christa, Stackhouse, Brian, Sloan, Arielle, Chen, Wenjie, Jensen, Nicole, Lien, Ju-Ping, Leslie, Richard, Johnson, Andrew D.
Published in Nucleic Acids Res (2014)

Associations of Prenatal Nicotine Exposure and the Dopamine Related Genes ANKK1 and DRD2 to Verbal Language

by Eicher, John D., Powers, Natalie R., Cho, Kelly, Miller, Laura L., Mueller, Kathryn L., Ring, Susan M., Tomblin, J. Bruce, Gruen, Jeffrey R.
Published 2013

Characterization of the platelet transcriptome by RNA sequencing in patients with acute myocardial infarction

by Eicher, John D., Wakabayashi, Yoshiyuki, Vitseva, Olga, Esa, Nada, Yang, Yanqin, Zhu, Jun, Freedman, Jane E., McManus, David D., Johnson, Andrew D.
Published in Platelets (2015)

Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability

by Cope, Natalie, Eicher, John D., Meng, Haiying, Gibson, Christopher J., Hager, Karl, Lacadie, Cheryl, Fulbright, Robert K., Constable, R. Todd, Page, Grier P., Gruen, Jeffrey R.
Published 2012

The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles

by Powers, Natalie R, Eicher, John D, Miller, Laura L, Kong, Yong, Smith, Shelley D, Pennington, Bruce F, Willcutt, Erik G, Olson, Richard K, Ring, Susan M, Gruen, Jeffrey R
Published in J Med Genet (2016)

Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ

by Eicher, John D., Powers, Natalie R., Miller, Laura L., Mueller, Kathryn L., Mascheretti, Sara, Marino, Cecilia, Willcutt, Erik G., DeFries, John C., Olson, Richard K., Smith, Shelley D., Pennington, Bruce F., Tomblin, J. Bruce, Ring, Susan M., Gruen, Jeffrey R.
Published 2014

Whole exome sequencing in the Framingham Heart Study identifies rare variation in HYAL2 that influences platelet aggregation

by Eicher, John D., Chen, Ming-Huei, Pitsillides, Achilleas N., Lin, Honghuang, Veeraraghavan, Narayanan, Brody, Jennifer A., Metcalf, Ginger A., Muzny, Donna M., Gibbs, Richard A., Becker, Diane M., Becker, Lewis C., Faraday, Nauder, Mathias, Rasika A., Yanek, Lisa R., Boerwinkle, Eric, Cupples, L. Adrienne, Johnson, Andrew D.
Published in Thromb Haemost (2017)

Exome-Chip Meta-Analysis Identifies Association between Variation in ANKRD26 and Platelet Aggregation

by Chen, Ming-Huei, Yanek, Lisa R., Backman, Joshua D., Eicher, John D., Huffman, Jennifer E., Ben-Shlomo, Yoav, Beswick, Andrew D., Yerges-Armstrong, Laura M., Shuldiner, Alan R., O’Connell, Jeffrey R., Mathias, Rasika A., Becker, Diane M., Becker, Lewis C., Lewis, Joshua P., Johnson, Andrew D., Faraday, Nauder
Published in Platelets (2017)

Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children

by Eicher, John D., Montgomery, Angela M., Akshoomoff, Natacha, Amaral, David G., Bloss, Cinnamon S., Libiger, Ondrej, Schork, Nicholas J., Darst, Burcu F., Casey, B. J., Chang, Linda, Ernst, Thomas, Frazier, Jean, Kaufmann, Walter E., Keating, Brian, Kenet, Tal, Kennedy, David, Mostofsky, Stewart, Murray, Sarah S., Sowell, Elizabeth R., Bartsch, Hauke, Kuperman, Joshua M., Brown, Timothy T., Hagler, Donald J., Dale, Anders M., Jernigan, Terry L., Gruen, Jeffrey R.
Published in Brain Imaging Behav (2015)

Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance

by Lotta, Luca A., Gulati, Pawan, Day, Felix R., Payne, Felicity, Ongen, Halit, van de Bunt, Martijn, Gaulton, Kyle J., Eicher, John D., Sharp, Stephen J., Luan, Jian’an, De Lucia Rolfe, Emanuella, Stewart, Isobel D., Wheeler, Eleanor, Willems, Sara M., Adams, Claire, Yaghootkar, Hanieh, Forouhi, Nita G., Khaw, Kay-Tee, Johnson, Andrew D., Semple, Robert K., Frayling, Timothy, Perry, John R. B., Dermitzakis, Emmanouil, McCarthy, Mark I., Barroso, Inês, Wareham, Nicholas J., Savage, David B., Langenberg, Claudia, O’Rahilly, Stephen, Scott, Robert A.
Published in Nat Genet (2016)

A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology

by de Vries, Paul S., Sabater-Lleal, Maria, Huffman, Jennifer E., Marten, Jonathan, Song, Ci, Pankratz, Nathan, Bartz, Traci M., de Haan, Hugoline G., Delgado, Graciela E., Eicher, John D., Martinez-Perez, Angel, Ward-Caviness, Cavin K., Brody, Jennifer A., Chen, Ming-Huei, de Maat, Moniek P. M., Frånberg, Mattias, Gill, Dipender, Kleber, Marcus E., Rivadeneira, Fernando, Soria, José Manuel, Tang, Weihong, Tofler, Geoffrey H., Uitterlinden, André G., van Hylckama Vlieg, Astrid, Seshadri, Sudha, Boerwinkle, Eric, Davies, Neil M., Giese, Anne-Katrin, Ikram, M. Kamran, Kittner, Steven J., McKnight, Barbara, Psaty, Bruce M., Reiner, Alex P., Sargurupremraj, Muralidharan, Taylor, Kent D., Fornage, Myriam, Hamsten, Anders, März, Winfried, Rosendaal, Frits R., Souto, Juan Carlos, Dehghan, Abbas, Johnson, Andrew D., Morrison, Alanna C., O'Donnell, Christopher J., Smith, Nicholas L.
Published in Blood (2019)

Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-wide Association Studies

by Joshi, Amit D., Andersson, Charlotte, Buch, Stephan, Stender, Stefan, Noordam, Raymond, Weng, Lu-Chen, Weeke, Peter E., Auer, Paul L., Boehm, Bernhard, Chen, Constance, Choi, Hyon, Curhan, Gary, Denny, Joshua C., De Vivo, Immaculata, Eicher, John D., Ellinghaus, David, Folsom, Aaron R., Fuchs, Charles, Gala, Manish, Haessler, Jeffrey, Hofman, Albert, Hu, Frank, Hunter, David J., Janssen, Harry L.A., Kang, Jae H., Kooperberg, Charles, Kraft, Peter, Kratzer, Wolfgang, Lieb, Wolfgang, Lutsey, Pamela L., Murad, Sarwa Darwish, Nordestgaard, Børge G., Pasquale, Louis R., Reiner, Alex P., Ridker, Paul M, Rimm, Eric, Rose, Lynda M., Shaffer, Christian M., Schafmayer, Clemens, Tamimi, Rulla M., Uitterlinden, André G, Völker, Uwe, Völzke, Henry, Wakabayashi, Yoshiyuki, Wiggs, Janey L., Zhu, Jun, Roden, Dan M., Stricker, Bruno H., Tang, Weihong, Teumer, Alexander, Hampe, Jochen, Tybjærg-Hansen, Anne, Chasman, Daniel I., Chan, Andrew T., Johnson, Andrew D.
Published in Gastroenterology (2016)

Large-scale pharmacogenomic study of sulfonylureas and the QT, JT, and QRS intervals: CHARGE Pharmacogenomics Working Group

by Floyd, James S, Sitlani, Colleen M, Avery, Christy L, Noordam, Raymond, Li, Xiaohui, Smith, Albert V, Gogarten, Stephanie M, Li, Jin, Broer, Linda, Evans, Daniel S, Trompet, Stella, Brody, Jennifer A, Stewart, James D, Eicher, John D, Seyerle, Amanda A, Roach, Jeffrey, Lange, Leslie A, Lin, Henry J, Kors, Jan A, Harris, Tamara B, Li-Gao, Ruifang, Sattar, Naveed, Cummings, Steven R, Wiggins, Kerri L, Napier, Melanie D, Stürmer, Til, Bis, Joshua C, Kerr, Kathleen F, Uitterlinden, André G, Taylor, Kent D, Stott, David J, de Mutsert, Renée, Launer, Lenore J, Busch, Evan L, Méndez-Giráldez, Raúl, Sotoodehnia, Nona, Soliman, Elsayed Z, Li, Yun, Duan, Qing, Rosendaal, Frits R, Slagboom, P Eline, Wilhelmsen, Kirk C, Reiner, Alexander P, Chen, Yii-Der I, Heckbert, Susan R, Kaplan, Robert C, Rice, Kenneth M, Jukema, J Wouter, Johnson, Andrew D, Liu, Yongmei, Mook-Kanamori, Dennis O, Gudnason, Vilmundur, Wilson, James G, Rotter, Jerome I, Laurie, Cathy C, Psaty, Bruce M, Whitsel, Eric A, Cupples, L Adrienne, Stricker, Bruno H
Published in Pharmacogenomics J (2016)

Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study

by Guerreiro, Rita, Ross, Owen A, Kun-Rodrigues, Celia, Hernandez, Dena G, Orme, Tatiana, Eicher, John D, Shepherd, Claire E, Parkkinen, Laura, Darwent, Lee, Heckman, Michael G, Scholz, Sonja W, Troncoso, Juan C, Pletnikova, Olga, Ansorge, Olaf, Clarimon, Jordi, Lleo, Alberto, Morenas-Rodriguez, Estrella, Clark, Lorraine, Honig, Lawrence S, Marder, Karen, Lemstra, Afina, Rogaeva, Ekaterina, St George-Hyslop, Peter, Londos, Elisabet, Zetterberg, Henrik, Barber, Imelda, Braae, Anne, Brown, Kristelle, Morgan, Kevin, Troakes, Claire, Al-Sarraj, Safa, Lashley, Tammaryn, Holton, Janice, Compta, Yaroslau, Van Deerlin, Vivianna, Serrano, Geidy E, Beach, Thomas G, Lesage, Suzanne, Galasko, Douglas, Masliah, Eliezer, Santana, Isabel, Pastor, Pau, Diez-Fairen, Monica, Aguilar, Miquel, Tienari, Pentti J, Myllykangas, Liisa, Oinas, Minna, Revesz, Tamas, Lees, Andrew, Boeve, Brad F, Petersen, Ronald C, Ferman, Tanis J, Escott-Price, Valentina, Graff-Radford, Neill, Cairns, Nigel J, Morris, John C, Pickering-Brown, Stuart, Mann, David, Halliday, Glenda M, Hardy, John, Trojanowski, John Q, Dickson, Dennis W, Singleton, Andrew, Stone, David J, Bras, Jose
Published in Lancet Neurol (2017)