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

di Eicher, John D., Gruen, Jeffrey R.
Pubblicazione 2013

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

di Eicher, John D., Gruen, Jeffrey R.
Pubblicato in Autism Res (2014)

The genetics of platelet count and volume in humans

di Eicher, John D., Lettre, Guillaume, Johnson, Andrew D.
Pubblicato in Platelets (2017)

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

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

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

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

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

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

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

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

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

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

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

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

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

di 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.
Pubblicazione 2012

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

di 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
Pubblicato in J Med Genet (2016)

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

di 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.
Pubblicazione 2014

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

di 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.
Pubblicato in Thromb Haemost (2017)

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

di 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
Pubblicato in Platelets (2017)

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

di 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.
Pubblicato in Brain Imaging Behav (2015)

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

di 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.
Pubblicato in Nat Genet (2016)

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

di 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.
Pubblicato in Blood (2019)

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

di 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.
Pubblicato in Gastroenterology (2016)

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

di 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
Pubblicato in Pharmacogenomics J (2016)

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

di 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
Pubblicato in Lancet Neurol (2017)