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

بواسطة Eicher, John D., Gruen, Jeffrey R.
منشور في 2013

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

بواسطة Eicher, John D., Gruen, Jeffrey R.
الحاوية / القاعدة Autism Res (2014)

The genetics of platelet count and volume in humans

بواسطة Eicher, John D., Lettre, Guillaume, Johnson, Andrew D.
الحاوية / القاعدة Platelets (2017)

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

بواسطة Eicher, John D., Xue, Luting, Ben-Shlomo, Yoav, Beswick, Andrew D., Johnson, Andrew D.
الحاوية / القاعدة J Thromb Thrombolysis (2016)

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

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

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

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

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

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

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

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

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

بواسطة Eicher, John D., Wakabayashi, Yoshiyuki, Vitseva, Olga, Esa, Nada, Yang, Yanqin, Zhu, Jun, Freedman, Jane E., McManus, David D., Johnson, Andrew D.
الحاوية / القاعدة Platelets (2015)

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

بواسطة 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.
منشور في 2012

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

بواسطة 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
الحاوية / القاعدة J Med Genet (2016)

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

بواسطة 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.
منشور في 2014

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

بواسطة 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.
الحاوية / القاعدة Thromb Haemost (2017)

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

بواسطة 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
الحاوية / القاعدة Platelets (2017)

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

بواسطة 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.
الحاوية / القاعدة Brain Imaging Behav (2015)

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

بواسطة 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.
الحاوية / القاعدة Nat Genet (2016)

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

بواسطة 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.
الحاوية / القاعدة Blood (2019)

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

بواسطة 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.
الحاوية / القاعدة Gastroenterology (2016)

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

بواسطة 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
الحاوية / القاعدة Pharmacogenomics J (2016)

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

بواسطة 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
الحاوية / القاعدة Lancet Neurol (2017)