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Effect of READ1 on latent profiles of reading disorder and comorbid attention and language impairment subtypes.

Li M, Truong DT, DeMille M, Malins JG, Lovett MW, Bosson-Heenan J, Gruen JR, Frijters JC.

Child Neuropsychol. 2019 Aug 14:1-25. doi: 10.1080/09297049.2019.1648642. [Epub ahead of print]


Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth.

Truong DT, Adams AK, Paniagua S, Frijters JC, Boada R, Hill DE, Lovett MW, Mahone EM, Willcutt EG, Wolf M, Defries JC, Gialluisi A, Francks C, Fisher SE, Olson RK, Pennington BF, Smith SD, Bosson-Heenan J, Gruen JR; Pediatric, Imaging, Neurocognition, and Genetics Consortium.

J Med Genet. 2019 Aug;56(8):557-566. doi: 10.1136/jmedgenet-2018-105874. Epub 2019 Apr 17.


Genetics of bronchopulmonary dysplasia: When things do not match up, it is only the beginning.

Bhandari V, Gruen JR, Jang KL, Göpel W, Hallman M, Lavoie PM.

J Pediatr. 2019 May;208:298-299. doi: 10.1016/j.jpeds.2019.01.014. Epub 2019 Feb 6. No abstract available.


A molecular-genetic and imaging-genetic approach to specific comprehension difficulties in children.

Li M, Malins JG, DeMille MMC, Lovett MW, Truong DT, Epstein K, Lacadie C, Mehta C, Bosson-Heenan J, Gruen JR, Frijters JC; GRaD Study Consortium.

NPJ Sci Learn. 2018 Nov 21;3:20. doi: 10.1038/s41539-018-0034-9. eCollection 2018.


Increased variability of stimulus-driven cortical responses is associated with genetic variability in children with and without dyslexia.

Centanni TM, Pantazis D, Truong DT, Gruen JR, Gabrieli JDE, Hogan TP.

Dev Cogn Neurosci. 2018 Nov;34:7-17. doi: 10.1016/j.dcn.2018.05.008. Epub 2018 May 26.


Worldwide distribution of the DCDC2 READ1 regulatory element and its relationship with phoneme variation across languages.

DeMille MMC, Tang K, Mehta CM, Geissler C, Malins JG, Powers NR, Bowen BM, Adams AK, Truong DT, Frijters JC, Gruen JR.

Proc Natl Acad Sci U S A. 2018 May 8;115(19):4951-4956. doi: 10.1073/pnas.1710472115. Epub 2018 Apr 16. Erratum in: Proc Natl Acad Sci U S A. 2018 May 21;:.


Reading-Related Causal Attributions for Success and Failure: Dynamic Links With Reading Skill.

Frijters JC, Tsujimoto KC, Boada R, Gottwald S, Hill D, Jacobson LA, Lovett MW, Mahone EM, Willcutt EG, Wolf M, Bosson-Heenan J, Gruen JR.

Read Res Q. 2018 Jan-Mar;53(1):127-148. doi: 10.1002/rrq.189. Epub 2017 Apr 29.


Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC.

Adams AK, Smith SD, Truong DT, Willcutt EG, Olson RK, DeFries JC, Pennington BF, Gruen JR.

Hum Genet. 2017 Nov;136(11-12):1395-1405. doi: 10.1007/s00439-017-1838-z. Epub 2017 Sep 2.


A method for integrating neuroimaging into genetic models of learning performance.

Mehta CM, Gruen JR, Zhang H.

Genet Epidemiol. 2017 Jan;41(1):4-17. doi: 10.1002/gepi.22025. Epub 2016 Nov 18.


Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders.

Truong DT, Shriberg LD, Smith SD, Chapman KL, Scheer-Cohen AR, DeMille MM, Adams AK, Nato AQ, Wijsman EM, Eicher JD, Gruen JR.

Hum Genet. 2016 Dec;135(12):1329-1341. Epub 2016 Aug 17.


Executive Functions Contribute Uniquely to Reading Competence in Minority Youth.

Jacobson LA, Koriakin T, Lipkin P, Boada R, Frijters JC, Lovett MW, Hill D, Willcutt E, Gottwald S, Wolf M, Bosson-Heenan J, Gruen JR, Mahone EM.

J Learn Disabil. 2017 Jul/Aug;50(4):422-433. doi: 10.1177/0022219415618501. Epub 2016 Jan 11.


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

Powers NR, Eicher JD, Miller LL, Kong Y, Smith SD, Pennington BF, Willcutt EG, Olson RK, Ring SM, Gruen JR.

J Med Genet. 2016 Mar;53(3):163-71. doi: 10.1136/jmedgenet-2015-103418. Epub 2015 Dec 11.


What is the basis for a genetic approach in neonatal disorders?

Bhandari V, Gruen JR.

Semin Perinatol. 2015 Dec;39(8):568-73. doi: 10.1053/j.semperi.2015.09.003. Epub 2015 Oct 23. Review.


Anxiety is related to indices of cortical maturation in typically developing children and adolescents.

Newman E, Thompson WK, Bartsch H, Hagler DJ Jr, Chen CH, Brown TT, Kuperman JM, McCabe C, Chung Y, Libiger O, Akshoomoff N, Bloss CS, Casey BJ, Chang L, Ernst TM, Frazier JA, Gruen JR, Kennedy DN, Murray SS, Sowell ER, Schork N, Kenet T, Kaufmann WE, Mostofsky S, Amaral DG, Dale AM, Jernigan TL.

Brain Struct Funct. 2016 Jul;221(6):3013-25. doi: 10.1007/s00429-015-1085-9. Epub 2015 Jul 17.


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

Eicher JD, Montgomery AM, Akshoomoff N, Amaral DG, Bloss CS, Libiger O, Schork NJ, Darst BF, Casey BJ, Chang L, Ernst T, Frazier J, Kaufmann WE, Keating B, Kenet T, Kennedy D, Mostofsky S, Murray SS, Sowell ER, Bartsch H, Kuperman JM, Brown TT, Hagler DJ Jr, Dale AM, Jernigan TL, Gruen JR; Pediatric Imaging Neurocognition Genetics Study.

Brain Imaging Behav. 2016 Mar;10(1):272-82. doi: 10.1007/s11682-015-9392-6.


The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository.

Jernigan TL, Brown TT, Hagler DJ Jr, Akshoomoff N, Bartsch H, Newman E, Thompson WK, Bloss CS, Murray SS, Schork N, Kennedy DN, Kuperman JM, McCabe C, Chung Y, Libiger O, Maddox M, Casey BJ, Chang L, Ernst TM, Frazier JA, Gruen JR, Sowell ER, Kenet T, Kaufmann WE, Mostofsky S, Amaral DG, Dale AM; Pediatric Imaging, Neurocognition and Genetics Study.

Neuroimage. 2016 Jan 1;124(Pt B):1149-1154. doi: 10.1016/j.neuroimage.2015.04.057. Epub 2015 May 1.


Family income, parental education and brain structure in children and adolescents.

Noble KG, Houston SM, Brito NH, Bartsch H, Kan E, Kuperman JM, Akshoomoff N, Amaral DG, Bloss CS, Libiger O, Schork NJ, Murray SS, Casey BJ, Chang L, Ernst TM, Frazier JA, Gruen JR, Kennedy DN, Van Zijl P, Mostofsky S, Kaufmann WE, Kenet T, Dale AM, Jernigan TL, Sowell ER.

Nat Neurosci. 2015 May;18(5):773-8. doi: 10.1038/nn.3983. Epub 2015 Mar 30.


The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains.

Eicher JD, Stein CM, Deng F, Ciesla AA, Powers NR, Boada R, Smith SD, Pennington BF, Iyengar SK, Lewis BA, Gruen JR.

Genes Brain Behav. 2015 Apr;14(4):377-85. doi: 10.1111/gbb.12214. Epub 2015 Apr 8.


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

Eicher JD, Gruen JR.

Autism Res. 2015 Apr;8(2):229-34. doi: 10.1002/aur.1436. Epub 2014 Dec 1.


The DCDC2/intron 2 deletion and white matter disorganization: focus on developmental dyslexia.

Marino C, Scifo P, Della Rosa PA, Mascheretti S, Facoetti A, Lorusso ML, Giorda R, Consonni M, Falini A, Molteni M, Gruen JR, Perani D.

Cortex. 2014 Aug;57:227-43. doi: 10.1016/j.cortex.2014.04.016. Epub 2014 May 9.


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

Eicher JD, Powers NR, Miller LL, Mueller KL, Mascheretti S, Marino C, Willcutt EG, DeFries JC, Olson RK, Smith SD, Pennington BF, Tomblin JB, Ring SM, Gruen JR.

Hum Genet. 2014 Jul;133(7):869-81. doi: 10.1007/s00439-014-1427-3. Epub 2014 Feb 9.


The NIH Toolbox Cognition Battery: results from a large normative developmental sample (PING).

Akshoomoff N, Newman E, Thompson WK, McCabe C, Bloss CS, Chang L, Amaral DG, Casey BJ, Ernst TM, Frazier JA, Gruen JR, Kaufmann WE, Kenet T, Kennedy DN, Libiger O, Mostofsky S, Murray SS, Sowell ER, Schork N, Dale AM, Jernigan TL.

Neuropsychology. 2014 Jan;28(1):1-10. doi: 10.1037/neu0000001. Epub 2013 Nov 11. Erratum in: Neuropsychology. 2014 Mar;28(2):319.


Genome-wide association study of shared components of reading disability and language impairment.

Eicher JD, Powers NR, Miller LL, Akshoomoff N, Amaral DG, Bloss CS, Libiger O, Schork NJ, Darst BF, Casey BJ, Chang L, Ernst T, Frazier J, Kaufmann WE, Keating B, Kenet T, Kennedy D, Mostofsky S, Murray SS, Sowell ER, Bartsch H, Kuperman JM, Brown TT, Hagler DJ Jr, Dale AM, Jernigan TL, St Pourcain B, Davey Smith G, Ring SM, Gruen JR; Pediatric Imaging, Neurocognition, and Genetics Study.

Genes Brain Behav. 2013 Nov;12(8):792-801. doi: 10.1111/gbb.12085. Epub 2013 Oct 9.


Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments.

Eicher JD, Gruen JR.

Mol Genet Metab. 2013 Nov;110(3):201-12. doi: 10.1016/j.ymgme.2013.07.001. Epub 2013 Jul 17. Review.


Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment.

Powers NR, Eicher JD, Butter F, Kong Y, Miller LL, Ring SM, Mann M, Gruen JR.

Am J Hum Genet. 2013 Jul 11;93(1):19-28. doi: 10.1016/j.ajhg.2013.05.008. Epub 2013 Jun 6. Erratum in: Am J Hum Genet. 2014 May 1;94(5):798.


Associations of prenatal nicotine exposure and the dopamine related genes ANKK1 and DRD2 to verbal language.

Eicher JD, Powers NR, Cho K, Miller LL, Mueller KL, Ring SM, Tomblin JB, Gruen JR.

PLoS One. 2013 May 15;8(5):e63762. doi: 10.1371/journal.pone.0063762. Print 2013.


Long-term influence of normal variation in neonatal characteristics on human brain development.

Walhovd KB, Fjell AM, Brown TT, Kuperman JM, Chung Y, Hagler DJ Jr, Roddey JC, Erhart M, McCabe C, Akshoomoff N, Amaral DG, Bloss CS, Libiger O, Schork NJ, Darst BF, Casey BJ, Chang L, Ernst TM, Frazier J, Gruen JR, Kaufmann WE, Murray SS, van Zijl P, Mostofsky S, Dale AM; Pediatric Imaging, Neurocognition, and Genetics Study.

Proc Natl Acad Sci U S A. 2012 Dec 4;109(49):20089-94. doi: 10.1073/pnas.1208180109. Epub 2012 Nov 19.


Multimodal imaging of the self-regulating developing brain.

Fjell AM, Walhovd KB, Brown TT, Kuperman JM, Chung Y, Hagler DJ Jr, Venkatraman V, Roddey JC, Erhart M, McCabe C, Akshoomoff N, Amaral DG, Bloss CS, Libiger O, Darst BF, Schork NJ, Casey BJ, Chang L, Ernst TM, Gruen JR, Kaufmann WE, Kenet T, Frazier J, Murray SS, Sowell ER, van Zijl P, Mostofsky S, Jernigan TL, Dale AM; Pediatric Imaging, Neurocognition, and Genetics Study.

Proc Natl Acad Sci U S A. 2012 Nov 27;109(48):19620-5. doi: 10.1073/pnas.1208243109. Epub 2012 Nov 12.


Prenatal exposure to nicotine and impaired reading performance.

Cho K, Frijters JC, Zhang H, Miller LL, Gruen JR.

J Pediatr. 2013 Apr;162(4):713-718.e2. doi: 10.1016/j.jpeds.2012.09.041. Epub 2012 Nov 2.


Neuroanatomical assessment of biological maturity.

Brown TT, Kuperman JM, Chung Y, Erhart M, McCabe C, Hagler DJ Jr, Venkatraman VK, Akshoomoff N, Amaral DG, Bloss CS, Casey BJ, Chang L, Ernst TM, Frazier JA, Gruen JR, Kaufmann WE, Kenet T, Kennedy DN, Murray SS, Sowell ER, Jernigan TL, Dale AM.

Curr Biol. 2012 Sep 25;22(18):1693-8. doi: 10.1016/j.cub.2012.07.002. Epub 2012 Aug 16.


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

Cope N, Eicher JD, Meng H, Gibson CJ, Hager K, Lacadie C, Fulbright RK, Constable RT, Page GP, Gruen JR.

Neuroimage. 2012 Oct 15;63(1):148-56. doi: 10.1016/j.neuroimage.2012.06.037. Epub 2012 Jun 27.


Genetic influences of resting state fMRI activity in language-related brain regions in healthy controls and schizophrenia patients: a pilot study.

Jamadar S, Powers NR, Meda SA, Calhoun VD, Gelernter J, Gruen JR, Pearlson GD.

Brain Imaging Behav. 2013 Mar;7(1):15-27. doi: 10.1007/s11682-012-9168-1.


Molecular diagnostic testing for Klinefelter syndrome and other male sex chromosome aneuploidies.

Hager K, Jennings K, Hosono S, Howell S, Gruen JR, Rivkees SA, Tartaglia NR, Rinder HM.

Int J Pediatr Endocrinol. 2012 Apr 23;2012(1):8. doi: 10.1186/1687-9856-2012-8.


Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans.

Bakken TE, Roddey JC, Djurovic S, Akshoomoff N, Amaral DG, Bloss CS, Casey BJ, Chang L, Ernst TM, Gruen JR, Jernigan TL, Kaufmann WE, Kenet T, Kennedy DN, Kuperman JM, Murray SS, Sowell ER, Rimol LM, Mattingsdal M, Melle I, Agartz I, Andreassen OA, Schork NJ, Dale AM; Alzheimer's Disease Neuroimaging Initiative; Pediatric Imaging, Neurocognition, and Genetics Study, Weiner M, Aisen P, Petersen R, Jack CR Jr, Jagust W, Trojanowki JQ, Toga AW, Beckett L, Green RC, Saykin AJ, Morris J, Liu E, Montine T, Gamst A, Thomas RG, Donohue M, Walter S, Gessert D, Sather T, Harvey D, Kornak J, Dale A, Bernstein M, Felmlee J, Fox N, Thompson P, Schuff N, Alexander G, DeCarli C, Bandy D, Koeppe RA, Foster N, Reiman EM, Chen K, Mathis C, Cairns NJ, Taylor-Reinwald L, Trojanowki JQ, Shaw L, Lee VM, Korecka M, Crawford K, Neu S, Foroud TM, Potkin S, Shen L, Kachaturian Z, Frank R, Snyder PJ, Molchan S, Kaye J, Quinn J, Lind B, Dolen S, Schneider LS, Pawluczyk S, Spann BM, Brewer J, Vanderswag H, Heidebrink JL, Lord JL, Johnson K, Doody RS, Villanueva-Meyer J, Chowdhury M, Stern Y, Honig LS, Bell KL, Morris JC, Ances B, Carroll M, Leon S, Mintun MA, Schneider S, Marson D, Griffith R, Clark D, Grossman H, Mitsis E, Romirowsky A, deToledo-Morrell L, Shah RC, Duara R, Varon D, Roberts P, Albert M, Onyike C, Kielb S, Rusinek H, de Leon MJ, Glodzik L, De Santi S, Doraiswamy PM, Petrella JR, Coleman RE, Arnold SE, Karlawish JH, Wolk D, Smith CD, Jicha G, Hardy P, Lopez OL, Oakley M, Simpson DM, Porsteinsson AP, Goldstein BS, Martin K, Makino KM, Ismail MS, Brand C, Mulnard RA, Thai G, Mc-Adams-Ortiz C, Womack K, Mathews D, Quiceno M, Diaz-Arrastia R, King R, Weiner M, Martin-Cook K, DeVous M, Levey AI, Lah JJ, Cellar JS, Burns JM, Anderson HS, Swerdlow RH, Apostolova L, Lu PH, Bartzokis G, Silverman DH, Graff-Radford NR, Parfitt F, Johnson H, Farlow MR, Hake AM, Matthews BR, Herring S, van Dyck CH, Carson RE, MacAvoy MG, Chertkow H, Bergman H, Hosein C, Black S, Stefanovic B, Caldwell C, Ging-Yuek, Hsiung R, Feldman H, Mudge B, Assaly M, Kertesz A, Rogers J, Trost D, Bernick C, Munic D, Kerwin D, Mesulam MM, Lipowski K, Wu CK, Johnson N, Sadowsky C, Martinez W, Villena T, Turner RS, Johnson K, Reynolds B, Sperling RA, Johnson KA, Marshall G, Frey M, Yesavage J, Taylor JL, Lane B, Rosen A, Tinklenberg J, Sabbagh M, Belden C, Jacobson S, Kowall N, Killiany R, Budson AE, Norbash A, Johnson PL, Obisesan TO, Wolday S, Bwayo SK, Lerner A, Hudson L, Ogrocki P, Fletcher E, Carmichael O, Olichney J, Kittur S, Borrie M, Lee TY, Bartha R, Johnson S, Asthana S, Carlsson CM, Potkin SG, Preda A, Nguyen D, Tariot P, Fleisher A, Reeder S, Bates V, Capote H, Rainka M, Scharre DW, Kataki M, Zimmerman EA, Celmins D, Brown AD, Pearlson GD, Blank K, Anderson K, Santulli RB, Schwartz ES, Sink KM, Williamson JD, Garg P, Watkins F, Ott BR, Querfurth H, Tremont G, Salloway S, Malloy P, Correia S, Rosen HJ, Miller BL, Mintzer J, Longmire CF, Spicer K, Finger E, Rachinsky I, Drost D, Jernigan T, McCabe C, Grant E, Ernst T, Kuperman J, Chung Y, Murray S, Bloss C, Darst B, Pritchett L, Saito A, Amaral D, DiNino M, Eyngorina B, Sowell E, Houston S, Soderberg L, Kaufmann W, van Zijl P, Rizzo-Busack H, Javid M, Mehta N, Ruberry E, Powers A, Rosen B, Gebhard N, Manigan H, Frazier J, Kennedy D, Yakutis L, Hill M, Gruen J, Bosson-Heenan J, Carlson H.

Proc Natl Acad Sci U S A. 2012 Mar 6;109(10):3985-90. doi: 10.1073/pnas.1105829109. Epub 2012 Feb 16.


DCDC2 genetic variants and susceptibility to developmental dyslexia.

Marino C, Meng H, Mascheretti S, Rusconi M, Cope N, Giorda R, Molteni M, Gruen JR.

Psychiatr Genet. 2012 Feb;22(1):25-30. doi: 10.1097/YPG.0b013e32834acdb2.


Genetic influences of cortical gray matter in language-related regions in healthy controls and schizophrenia.

Jamadar S, Powers NR, Meda SA, Gelernter J, Gruen JR, Pearlson GD.

Schizophr Res. 2011 Jul;129(2-3):141-8. doi: 10.1016/j.schres.2011.03.027. Epub 2011 Apr 20.


A highly sensitive, high-throughput assay for the detection of Turner syndrome.

Rivkees SA, Hager K, Hosono S, Wise A, Li P, Rinder HM, Gruen JR.

J Clin Endocrinol Metab. 2011 Mar;96(3):699-705. doi: 10.1210/jc.2010-1554. Epub 2010 Dec 22.


Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia.

Marino C, Mascheretti S, Riva V, Cattaneo F, Rigoletto C, Rusconi M, Gruen JR, Giorda R, Lazazzera C, Molteni M.

Behav Genet. 2011 Jan;41(1):67-76. doi: 10.1007/s10519-010-9412-7. Epub 2010 Nov 3.


A dyslexia-associated variant in DCDC2 changes gene expression.

Meng H, Powers NR, Tang L, Cope NA, Zhang PX, Fuleihan R, Gibson C, Page GP, Gruen JR.

Behav Genet. 2011 Jan;41(1):58-66. doi: 10.1007/s10519-010-9408-3. Epub 2010 Nov 2.


The impact of environmental and genetic factors on neonatal late-onset sepsis.

Bizzarro MJ, Jiang Y, Hussain N, Gruen JR, Bhandari V, Zhang H.

J Pediatr. 2011 Feb;158(2):234-8.e1. doi: 10.1016/j.jpeds.2010.07.060. Epub 2010 Sep 17.


Functional impact of a single-nucleotide polymorphism in the OPRD1 promoter region.

Zhang H, Gelernter J, Gruen JR, Kranzler HR, Herman AI, Simen AA.

J Hum Genet. 2010 May;55(5):278-84. doi: 10.1038/jhg.2010.22. Epub 2010 Mar 19.


The genetic susceptibility to respiratory distress syndrome.

Levit O, Jiang Y, Bizzarro MJ, Hussain N, Buhimschi CS, Gruen JR, Zhang H, Bhandari V.

Pediatr Res. 2009 Dec;66(6):693-7. doi: 10.1203/PDR.0b013e3181bbce86.


Progress towards a cellular neurobiology of reading disability.

Gabel LA, Gibson CJ, Gruen JR, LoTurco JJ.

Neurobiol Dis. 2010 May;38(2):173-80. doi: 10.1016/j.nbd.2009.06.019. Epub 2009 Jul 17. Review.


Cognitive flexibility is associated with KIBRA variant and modulated by recent tobacco use.

Zhang H, Kranzler HR, Poling J, Gruen JR, Gelernter J.

Neuropsychopharmacology. 2009 Nov;34(12):2508-16. doi: 10.1038/npp.2009.80. Epub 2009 Jul 15.


Genetic contribution to patent ductus arteriosus in the premature newborn.

Bhandari V, Zhou G, Bizzarro MJ, Buhimschi C, Hussain N, Gruen JR, Zhang H.

Pediatrics. 2009 Feb;123(2):669-73. doi: 10.1542/peds.2008-1117.


Polymorphism of DCDC2 Reveals Differences in Cortical Morphology of Healthy Individuals-A Preliminary Voxel Based Morphometry Study.

Meda SA, Gelernter J, Gruen JR, Calhoun VD, Meng H, Cope NA, Pearlson GD.

Brain Imaging Behav. 2008 Mar;2(1):21-26.


Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample.

Ludwig KU, Schumacher J, Schulte-Körne G, König IR, Warnke A, Plume E, Anthoni H, Peyrard-Janvid M, Meng H, Ziegler A, Remschmidt H, Kere J, Gruen JR, Müller-Myhsok B, Nöthen MM, Hoffmann P.

Psychiatr Genet. 2008 Dec;18(6):310-2. doi: 10.1097/YPG.0b013e3283063a78.


Haplotypic variants in DRD2, ANKK1, TTC12, and NCAM1 are associated with comorbid alcohol and drug dependence.

Yang BZ, Kranzler HR, Zhao H, Gruen JR, Luo X, Gelernter J.

Alcohol Clin Exp Res. 2008 Dec;32(12):2117-27. doi: 10.1111/j.1530-0277.2008.00800.x. Epub 2008 Sep 30.


The human lexinome: genes of language and reading.

Gibson CJ, Gruen JR.

J Commun Disord. 2008 Sep-Oct;41(5):409-20. doi: 10.1016/j.jcomdis.2008.03.003. Epub 2008 Mar 25. Review.


Association of haplotypic variants in DRD2, ANKK1, TTC12 and NCAM1 to alcohol dependence in independent case control and family samples.

Yang BZ, Kranzler HR, Zhao H, Gruen JR, Luo X, Gelernter J.

Hum Mol Genet. 2007 Dec 1;16(23):2844-53. Epub 2007 Aug 30.


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