Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 78

1.

Autism Heterogeneity in a Densely Sampled U.S. Population: Results From the First 1,000 Participants in the RI-CART Study.

McCormick CEB, Kavanaugh BC, Sipsock D, Righi G, Oberman LM, Moreno De Luca D, Gamsiz Uzun ED, Best CR, Jerskey BA, Quinn JG, Jewel SB, Wu PC, McLean RL, Levine TP, Tokadjian H, Perkins KA, Clarke EB, Dunn B, Gerber AH, Tenenbaum EJ, Anders TF; Rhode Island Consortium for Autism Research and Treatment (RI-CART), Sheinkopf SJ, Morrow EM.

Autism Res. 2020 Mar;13(3):474-488. doi: 10.1002/aur.2261. Epub 2020 Jan 20.

PMID:
31957984
2.

Paternal sperm DNA mosaicism and recurrence risk of autism in families.

Morrow EM.

Nat Med. 2020 Jan;26(1):26-28. doi: 10.1038/s41591-019-0732-8. No abstract available.

PMID:
31873313
3.

Functional Assessment In Vivo of the Mouse Homolog of the Human Ala-9-Ser NHE6 Variant.

Ouyang Q, Joesch-Cohen L, Mishra S, Riaz HA, Schmidt M, Morrow EM.

eNeuro. 2019 Dec 4;6(6). pii: ENEURO.0046-19.2019. doi: 10.1523/ENEURO.0046-19.2019. Print 2019 Nov/Dec.

4.

GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates.

Ouyang Q, Kavanaugh BC, Joesch-Cohen L, Dubois B, Wu Q, Schmidt M, Baytas O, Pastore SF, Harripaul R, Mishra S, Hussain A, Kim KH, Holler-Managan YF, Ayub M, Mir A, Vincent JB, Liu JS, Morrow EM.

Hum Genet. 2019 Oct;138(10):1183-1200. doi: 10.1007/s00439-019-02057-x. Epub 2019 Aug 30.

PMID:
31471722
5.

Longitudinal MRI findings in patient with SLC25A12 pathogenic variants inform disease progression and classification.

Kavanaugh BC, Warren EB, Baytas O, Schmidt M, Merck D, Buch K, Liu JS, Phornphutkul C, Caruso P, Morrow EM.

Am J Med Genet A. 2019 Nov;179(11):2284-2291. doi: 10.1002/ajmg.a.61322. Epub 2019 Aug 12.

PMID:
31403263
6.

Mitochondrial Function in 22q11 Deletion Syndrome.

Warren EB, Morrow EM.

Neuron. 2019 Jun 19;102(6):1089-1091. doi: 10.1016/j.neuron.2019.05.052.

PMID:
31220439
7.

Complex Neurological Phenotype in Female Carriers of NHE6 Mutations.

Pescosolido MF, Kavanaugh BC, Pochet N, Schmidt M, Jerskey BA, Rogg JM, De Jager PL, Young-Pearse TL, Liu JS, Morrow EM.

Mol Neuropsychiatry. 2019 Apr;5(2):98-108. doi: 10.1159/000496341. Epub 2019 Mar 6.

8.

Strong correlation of downregulated genes related to synaptic transmission and mitochondria in post-mortem autism cerebral cortex.

Schwede M, Nagpal S, Gandal MJ, Parikshak NN, Mirnics K, Geschwind DH, Morrow EM.

J Neurodev Disord. 2018 Jun 1;10(1):18. doi: 10.1186/s11689-018-9237-x.

9.

Mixed Neurodevelopmental and Neurodegenerative Pathology in Nhe6-Null Mouse Model of Christianson Syndrome.

Xu M, Ouyang Q, Gong J, Pescosolido MF, Pruett BS, Mishra S, Schmidt M, Jones RN, Gamsiz Uzun ED, Lizarraga SB, Morrow EM.

eNeuro. 2018 Jan 17;4(6). pii: ENEURO.0388-17.2017. doi: 10.1523/ENEURO.0388-17.2017. eCollection 2017 Nov-Dec.

10.

Christianson Syndrome.

Morrow EM, Pescosolido MF.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2020.
2018 Jan 11.

11.

The Role of Mitochondrial Glutamate Metabolism in Cognitive Development and Disease.

Baytaş O, Morrow EM.

Neuropsychopharmacology. 2018 Jan;43(1):229-230. doi: 10.1038/npp.2017.202. No abstract available.

12.

Live-cell Microscopy and Fluorescence-based Measurement of Luminal pH in Intracellular Organelles.

Ma L, Ouyang Q, Werthmann GC, Thompson HM, Morrow EM.

Front Cell Dev Biol. 2017 Aug 21;5:71. doi: 10.3389/fcell.2017.00071. eCollection 2017.

13.

Predictors of Inpatient Psychiatric Hospitalization for Children and Adolescents with Autism Spectrum Disorder.

Righi G, Benevides J, Mazefsky C, Siegel M, Sheinkopf SJ, Morrow EM; Autism and Developmental Disabilities Inpatient Research Collaborative (ADDIRC).

J Autism Dev Disord. 2018 Nov;48(11):3647-3657. doi: 10.1007/s10803-017-3154-9.

14.

Characterization of Medication Use in a Multicenter Sample of Pediatric Inpatients with Autism Spectrum Disorder.

Wink LK, Pedapati EV, Adams R, Erickson CA, Pedersen KA, Morrow EM, Kaplan D, Siegel M; Autism and Developmental Disorders Inpatient Research Collaborative (ADDIRC).

J Autism Dev Disord. 2018 Nov;48(11):3711-3719. doi: 10.1007/s10803-017-3153-x.

PMID:
28516426
15.

Brief Report: Factors Influencing Healthcare Satisfaction in Adults with Autism Spectrum Disorder.

Gerber AH, McCormick CEB, Levine TP, Morrow EM, Anders TF, Sheinkopf SJ.

J Autism Dev Disord. 2017 Jun;47(6):1896-1903. doi: 10.1007/s10803-017-3087-3.

PMID:
28271179
16.

Supportive care for older people with frailty in hospital: An integrative review.

Nicholson C, Morrow EM, Hicks A, Fitzpatrick J.

Int J Nurs Stud. 2017 Jan;66:60-71. doi: 10.1016/j.ijnurstu.2016.11.015. Epub 2016 Nov 24. Review.

17.

Genetic control of postnatal human brain growth.

van Dyck LI, Morrow EM.

Curr Opin Neurol. 2017 Feb;30(1):114-124. doi: 10.1097/WCO.0000000000000405. Review.

18.

Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive features.

Ouyang Q, Nakayama T, Baytas O, Davidson SM, Yang C, Schmidt M, Lizarraga SB, Mishra S, Ei-Quessny M, Niaz S, Gul Butt M, Imran Murtaza S, Javed A, Chaudhry HR, Vaughan DJ, Hill RS, Partlow JN, Yoo SY, Lam AT, Nasir R, Al-Saffar M, Barkovich AJ, Schwede M, Nagpal S, Rajab A, DeBerardinis RJ, Housman DE, Mochida GH, Morrow EM.

Proc Natl Acad Sci U S A. 2016 Sep 20;113(38):E5598-607. doi: 10.1073/pnas.1609221113. Epub 2016 Sep 6.

19.

Carer engagement in the hospital care of older people: an integrative literature review.

Morrow EM, Nicholson C.

Int J Older People Nurs. 2016 Dec;11(4):298-314. doi: 10.1111/opn.12117. Epub 2016 Feb 25. Review.

20.

Graph Metrics of Structural Brain Networks in Individuals with Schizophrenia and Healthy Controls: Group Differences, Relationships with Intelligence, and Genetics.

Yeo RA, Ryman SG, van den Heuvel MP, de Reus MA, Jung RE, Pommy J, Mayer AR, Ehrlich S, Schulz SC, Morrow EM, Manoach D, Ho BC, Sponheim SR, Calhoun VD.

J Int Neuropsychol Soc. 2016 Feb;22(2):240-9. doi: 10.1017/S1355617715000867.

PMID:
26888620
21.

Creating Patient-Specific Neural Cells for the In Vitro Study of Brain Disorders.

Brennand KJ, Marchetto MC, Benvenisty N, Brüstle O, Ebert A, Izpisua Belmonte JC, Kaykas A, Lancaster MA, Livesey FJ, McConnell MJ, McKay RD, Morrow EM, Muotri AR, Panchision DM, Rubin LL, Sawa A, Soldner F, Song H, Studer L, Temple S, Vaccarino FM, Wu J, Vanderhaeghen P, Gage FH, Jaenisch R.

Stem Cell Reports. 2015 Dec 8;5(6):933-945. doi: 10.1016/j.stemcr.2015.10.011. Epub 2015 Nov 21.

22.

The autism inpatient collection: methods and preliminary sample description.

Siegel M, Smith KA, Mazefsky C, Gabriels RL, Erickson C, Kaplan D, Morrow EM, Wink L, Santangelo SL; Autism and Developmental Disorders Inpatient Research Collaborative (ADDIRC).

Mol Autism. 2015 Nov 10;6:61. doi: 10.1186/s13229-015-0054-8. eCollection 2015.

23.

Modeling developmental neuropsychiatric disorders with iPSC technology: challenges and opportunities.

Young-Pearse TL, Morrow EM.

Curr Opin Neurobiol. 2016 Feb;36:66-73. doi: 10.1016/j.conb.2015.10.006. Epub 2015 Oct 24. Review.

24.

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.

Sanders SJ, He X, Willsey AJ, Ercan-Sencicek AG, Samocha KE, Cicek AE, Murtha MT, Bal VH, Bishop SL, Dong S, Goldberg AP, Jinlu C, Keaney JF 3rd, Klei L, Mandell JD, Moreno-De-Luca D, Poultney CS, Robinson EB, Smith L, Solli-Nowlan T, Su MY, Teran NA, Walker MF, Werling DM, Beaudet AL, Cantor RM, Fombonne E, Geschwind DH, Grice DE, Lord C, Lowe JK, Mane SM, Martin DM, Morrow EM, Talkowski ME, Sutcliffe JS, Walsh CA, Yu TW; Autism Sequencing Consortium, Ledbetter DH, Martin CL, Cook EH, Buxbaum JD, Daly MJ, Devlin B, Roeder K, State MW.

Neuron. 2015 Sep 23;87(6):1215-1233. doi: 10.1016/j.neuron.2015.09.016.

25.

Uncovering a Role for SK2 in Angelman Syndrome.

Lizarraga SB, Morrow EM.

Cell Rep. 2015 Jul 21;12(3):359-60. doi: 10.1016/j.celrep.2015.07.009.

26.

Discovery of Rare Mutations in Autism: Elucidating Neurodevelopmental Mechanisms.

Gamsiz ED, Sciarra LN, Maguire AM, Pescosolido MF, van Dyck LI, Morrow EM.

Neurotherapeutics. 2015 Jul;12(3):553-71. doi: 10.1007/s13311-015-0363-9. Review.

27.

Female Autism Phenotypes Investigated at Different Levels of Language and Developmental Abilities.

Howe YJ, O'Rourke JA, Yatchmink Y, Viscidi EW, Jones RN, Morrow EM.

J Autism Dev Disord. 2015 Nov;45(11):3537-49. doi: 10.1007/s10803-015-2501-y.

28.

A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?

Chaste P, Klei L, Sanders SJ, Hus V, Murtha MT, Lowe JK, Willsey AJ, Moreno-De-Luca D, Yu TW, Fombonne E, Geschwind D, Grice DE, Ledbetter DH, Mane SM, Martin DM, Morrow EM, Walsh CA, Sutcliffe JS, Lese Martin C, Beaudet AL, Lord C, State MW, Cook EH Jr, Devlin B.

Biol Psychiatry. 2015 May 1;77(9):775-84. doi: 10.1016/j.biopsych.2014.09.017. Epub 2014 Sep 30.

29.

MicroRNAs in copy number variants in schizophrenia: misregulation of genome-wide gene expression programs.

Morrow EM.

Biol Psychiatry. 2015 Jan 15;77(2):93-4. doi: 10.1016/j.biopsych.2014.11.006. No abstract available.

PMID:
25524307
30.

Quantifying the effects of rare variants in pedigrees: how far does the apple fall from the tree?

Morrow EM.

JAMA Psychiatry. 2015 Feb;72(2):106-7. doi: 10.1001/jamapsychiatry.2014.2442. No abstract available.

PMID:
25493613
31.

Inaugural Christianson Syndrome Association conference: families meeting for the first time.

Stein DM, Gerber A, Morrow EM.

J Neurodev Disord. 2014;6(1):13. doi: 10.1186/1866-1955-6-13. Epub 2014 May 23.

32.

Observation-centered approach to ASD assessment in Tanzania.

Harrison AJ, Zimak EH, Sheinkopf SJ, Manji KP, Morrow EM.

Intellect Dev Disabil. 2014 Oct;52(5):330-47. doi: 10.1352/1934-9556-52.5.330.

PMID:
25247726
33.

Executive function in probands with autism with average IQ and their unaffected first-degree relatives.

McLean RL, Johnson Harrison A, Zimak E, Joseph RM, Morrow EM.

J Am Acad Child Adolesc Psychiatry. 2014 Sep;53(9):1001-9. doi: 10.1016/j.jaac.2014.05.019. Epub 2014 Jul 11.

34.

Expansion of the clinical phenotype associated with mutations in activity-dependent neuroprotective protein.

Pescosolido MF, Schwede M, Johnson Harrison A, Schmidt M, Gamsiz ED, Chen WS, Donahue JP, Shur N, Jerskey BA, Phornphutkul C, Morrow EM.

J Med Genet. 2014 Sep;51(9):587-9. doi: 10.1136/jmedgenet-2014-102444. Epub 2014 Jul 23. No abstract available.

35.

Genetic and phenotypic diversity of NHE6 mutations in Christianson syndrome.

Pescosolido MF, Stein DM, Schmidt M, El Achkar CM, Sabbagh M, Rogg JM, Tantravahi U, McLean RL, Liu JS, Poduri A, Morrow EM.

Ann Neurol. 2014 Oct;76(4):581-93. doi: 10.1002/ana.24225. Epub 2014 Sep 19.

36.

Ascertainment and gender in autism spectrum disorders.

Howe YJ, Yatchmink Y, Viscidi EW, Morrow EM.

J Am Acad Child Adolesc Psychiatry. 2014 Jun;53(6):698-700. doi: 10.1016/j.jaac.2014.04.003. No abstract available.

37.

Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.

Chaste P, Sanders SJ, Mohan KN, Klei L, Song Y, Murtha MT, Hus V, Lowe JK, Willsey AJ, Moreno-De-Luca D, Yu TW, Fombonne E, Geschwind D, Grice DE, Ledbetter DH, Lord C, Mane SM, Martin DM, Morrow EM, Walsh CA, Sutcliffe JS, State MW, Martin CL, Devlin B, Beaudet AL, Cook EH Jr, Kim SJ.

Autism Res. 2014 Jun;7(3):355-62. doi: 10.1002/aur.1378. Epub 2014 May 12.

38.

Genetic influences on cognitive endophenotypes in schizophrenia.

Yeo RA, Gangestad SW, Walton E, Ehrlich S, Pommy J, Turner JA, Liu J, Mayer AR, Schulz SC, Ho BC, Bustillo JR, Wassink TH, Sponheim SR, Morrow EM, Calhoun VD.

Schizophr Res. 2014 Jun;156(1):71-5. doi: 10.1016/j.schres.2014.03.022. Epub 2014 Apr 24.

39.

The association between epilepsy and autism symptoms and maladaptive behaviors in children with autism spectrum disorder.

Viscidi EW, Johnson AL, Spence SJ, Buka SL, Morrow EM, Triche EW.

Autism. 2014 Nov;18(8):996-1006. doi: 10.1177/1362361313508027. Epub 2013 Oct 28.

40.

SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs).

Abrahams BS, Arking DE, Campbell DB, Mefford HC, Morrow EM, Weiss LA, Menashe I, Wadkins T, Banerjee-Basu S, Packer A.

Mol Autism. 2013 Oct 3;4(1):36. doi: 10.1186/2040-2392-4-36.

41.

Christianson syndrome protein NHE6 modulates TrkB endosomal signaling required for neuronal circuit development.

Ouyang Q, Lizarraga SB, Schmidt M, Yang U, Gong J, Ellisor D, Kauer JA, Morrow EM.

Neuron. 2013 Oct 2;80(1):97-112. doi: 10.1016/j.neuron.2013.07.043. Epub 2013 Sep 12.

42.

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.

Cross-Disorder Group of the Psychiatric Genomics Consortium, Lee SH, Ripke S, Neale BM, Faraone SV, Purcell SM, Perlis RH, Mowry BJ, Thapar A, Goddard ME, Witte JS, Absher D, Agartz I, Akil H, Amin F, Andreassen OA, Anjorin A, Anney R, Anttila V, Arking DE, Asherson P, Azevedo MH, Backlund L, Badner JA, Bailey AJ, Banaschewski T, Barchas JD, Barnes MR, Barrett TB, Bass N, Battaglia A, Bauer M, Bayés M, Bellivier F, Bergen SE, Berrettini W, Betancur C, Bettecken T, Biederman J, Binder EB, Black DW, Blackwood DH, Bloss CS, Boehnke M, Boomsma DI, Breen G, Breuer R, Bruggeman R, Cormican P, Buccola NG, Buitelaar JK, Bunney WE, Buxbaum JD, Byerley WF, Byrne EM, Caesar S, Cahn W, Cantor RM, Casas M, Chakravarti A, Chambert K, Choudhury K, Cichon S, Cloninger CR, Collier DA, Cook EH, Coon H, Cormand B, Corvin A, Coryell WH, Craig DW, Craig IW, Crosbie J, Cuccaro ML, Curtis D, Czamara D, Datta S, Dawson G, Day R, De Geus EJ, Degenhardt F, Djurovic S, Donohoe GJ, Doyle AE, Duan J, Dudbridge F, Duketis E, Ebstein RP, Edenberg HJ, Elia J, Ennis S, Etain B, Fanous A, Farmer AE, Ferrier IN, Flickinger M, Fombonne E, Foroud T, Frank J, Franke B, Fraser C, Freedman R, Freimer NB, Freitag CM, Friedl M, Frisén L, Gallagher L, Gejman PV, Georgieva L, Gershon ES, Geschwind DH, Giegling I, Gill M, Gordon SD, Gordon-Smith K, Green EK, Greenwood TA, Grice DE, Gross M, Grozeva D, Guan W, Gurling H, De Haan L, Haines JL, Hakonarson H, Hallmayer J, Hamilton SP, Hamshere ML, Hansen TF, Hartmann AM, Hautzinger M, Heath AC, Henders AK, Herms S, Hickie IB, Hipolito M, Hoefels S, Holmans PA, Holsboer F, Hoogendijk WJ, Hottenga JJ, Hultman CM, Hus V, Ingason A, Ising M, Jamain S, Jones EG, Jones I, Jones L, Tzeng JY, Kähler AK, Kahn RS, Kandaswamy R, Keller MC, Kennedy JL, Kenny E, Kent L, Kim Y, Kirov GK, Klauck SM, Klei L, Knowles JA, Kohli MA, Koller DL, Konte B, Korszun A, Krabbendam L, Krasucki R, Kuntsi J, Kwan P, Landén M, Långström N, Lathrop M, Lawrence J, Lawson WB, Leboyer M, Ledbetter DH, Lee PH, Lencz T, Lesch KP, Levinson DF, Lewis CM, Li J, Lichtenstein P, Lieberman JA, Lin DY, Linszen DH, Liu C, Lohoff FW, Loo SK, Lord C, Lowe JK, Lucae S, MacIntyre DJ, Madden PA, Maestrini E, Magnusson PK, Mahon PB, Maier W, Malhotra AK, Mane SM, Martin CL, Martin NG, Mattheisen M, Matthews K, Mattingsdal M, McCarroll SA, McGhee KA, McGough JJ, McGrath PJ, McGuffin P, McInnis MG, McIntosh A, McKinney R, McLean AW, McMahon FJ, McMahon WM, McQuillin A, Medeiros H, Medland SE, Meier S, Melle I, Meng F, Meyer J, Middeldorp CM, Middleton L, Milanova V, Miranda A, Monaco AP, Montgomery GW, Moran JL, Moreno-De-Luca D, Morken G, Morris DW, Morrow EM, Moskvina V, Muglia P, Mühleisen TW, Muir WJ, Müller-Myhsok B, Murtha M, Myers RM, Myin-Germeys I, Neale MC, Nelson SF, Nievergelt CM, Nikolov I, Nimgaonkar V, Nolen WA, Nöthen MM, Nurnberger JI, Nwulia EA, Nyholt DR, O'Dushlaine C, Oades RD, Olincy A, Oliveira G, Olsen L, Ophoff RA, Osby U, Owen MJ, Palotie A, Parr JR, Paterson AD, Pato CN, Pato MT, Penninx BW, Pergadia ML, Pericak-Vance MA, Pickard BS, Pimm J, Piven J, Posthuma D, Potash JB, Poustka F, Propping P, Puri V, Quested DJ, Quinn EM, Ramos-Quiroga JA, Rasmussen HB, Raychaudhuri S, Rehnström K, Reif A, Ribasés M, Rice JP, Rietschel M, Roeder K, Roeyers H, Rossin L, Rothenberger A, Rouleau G, Ruderfer D, Rujescu D, Sanders AR, Sanders SJ, Santangelo SL, Sergeant JA, Schachar R, Schalling M, Schatzberg AF, Scheftner WA, Schellenberg GD, Scherer SW, Schork NJ, Schulze TG, Schumacher J, Schwarz M, Scolnick E, Scott LJ, Shi J, Shilling PD, Shyn SI, Silverman JM, Slager SL, Smalley SL, Smit JH, Smith EN, Sonuga-Barke EJ, St Clair D, State M, Steffens M, Steinhausen HC, Strauss JS, Strohmaier J, Stroup TS, Sutcliffe JS, Szatmari P, Szelinger S, Thirumalai S, Thompson RC, Todorov AA, Tozzi F, Treutlein J, Uhr M, van den Oord EJ, Van Grootheest G, Van Os J, Vicente AM, Vieland VJ, Vincent JB, Visscher PM, Walsh CA, Wassink TH, Watson SJ, Weissman MM, Werge T, Wienker TF, Wijsman EM, Willemsen G, Williams N, Willsey AJ, Witt SH, Xu W, Young AH, Yu TW, Zammit S, Zandi PP, Zhang P, Zitman FG, Zöllner S, Devlin B, Kelsoe JR, Sklar P, Daly MJ, O'Donovan MC, Craddock N, Sullivan PF, Smoller JW, Kendler KS, Wray NR; International Inflammatory Bowel Disease Genetics Consortium (IIBDGC).

Nat Genet. 2013 Sep;45(9):984-94. doi: 10.1038/ng.2711. Epub 2013 Aug 11.

43.

Clinical characteristics of children with autism spectrum disorder and co-occurring epilepsy.

Viscidi EW, Triche EW, Pescosolido MF, McLean RL, Joseph RM, Spence SJ, Morrow EM.

PLoS One. 2013 Jul 4;8(7):e67797. doi: 10.1371/journal.pone.0067797. Print 2013.

44.

Intellectual disability is associated with increased runs of homozygosity in simplex autism.

Gamsiz ED, Viscidi EW, Frederick AM, Nagpal S, Sanders SJ, Murtha MT, Schmidt M; Simons Simplex Collection Genetics Consortium, Triche EW, Geschwind DH, State MW, Istrail S, Cook EH Jr, Devlin B, Morrow EM.

Am J Hum Genet. 2013 Jul 11;93(1):103-9. doi: 10.1016/j.ajhg.2013.06.004. Epub 2013 Jul 3.

45.

Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait.

Chaste P, Klei L, Sanders SJ, Murtha MT, Hus V, Lowe JK, Willsey AJ, Moreno-De-Luca D, Yu TW, Fombonne E, Geschwind D, Grice DE, Ledbetter DH, Lord C, Mane SM, Lese Martin C, Martin DM, Morrow EM, Walsh CA, Sutcliffe JS, State MW, Devlin B, Cook EH Jr, Kim SJ.

Biol Psychiatry. 2013 Oct 15;74(8):576-84. doi: 10.1016/j.biopsych.2013.04.018. Epub 2013 Jun 6.

46.

Distribution of disease-associated copy number variants across distinct disorders of cognitive development.

Pescosolido MF, Gamsiz ED, Nagpal S, Morrow EM.

J Am Acad Child Adolesc Psychiatry. 2013 Apr;52(4):414-430.e14. doi: 10.1016/j.jaac.2013.01.003. Review.

47.

Genes for endosomal NHE6 and NHE9 are misregulated in autism brains.

Schwede M, Garbett K, Mirnics K, Geschwind DH, Morrow EM.

Mol Psychiatry. 2014 Mar;19(3):277-9. doi: 10.1038/mp.2013.28. Epub 2013 Mar 19. No abstract available.

48.

An unbalanced translocation involving loss of 10q26.2 and gain of 11q25 in a pedigree with autism spectrum disorder and cerebellar juvenile pilocytic astrocytoma.

Minhas HM, Pescosolido MF, Schwede M, Piasecka J, Gaitanis J, Tantravahi U, Morrow EM.

Am J Med Genet A. 2013 Apr;161A(4):787-91. doi: 10.1002/ajmg.a.35841. Epub 2013 Mar 12.

49.

Risk assessment models in genetics clinic for array comparative genomic hybridization: Clinical information can be used to predict the likelihood of an abnormal result in patients.

Marano RM, Mercurio L, Kanter R, Doyle R, Abuelo D, Morrow EM, Shur N.

J Pediatr Genet. 2013 Mar;2(1):25-31. doi: 10.3233/PGE-13044.

50.

Using whole-exome sequencing to identify inherited causes of autism.

Yu TW, Chahrour MH, Coulter ME, Jiralerspong S, Okamura-Ikeda K, Ataman B, Schmitz-Abe K, Harmin DA, Adli M, Malik AN, D'Gama AM, Lim ET, Sanders SJ, Mochida GH, Partlow JN, Sunu CM, Felie JM, Rodriguez J, Nasir RH, Ware J, Joseph RM, Hill RS, Kwan BY, Al-Saffar M, Mukaddes NM, Hashmi A, Balkhy S, Gascon GG, Hisama FM, LeClair E, Poduri A, Oner O, Al-Saad S, Al-Awadi SA, Bastaki L, Ben-Omran T, Teebi AS, Al-Gazali L, Eapen V, Stevens CR, Rappaport L, Gabriel SB, Markianos K, State MW, Greenberg ME, Taniguchi H, Braverman NE, Morrow EM, Walsh CA.

Neuron. 2013 Jan 23;77(2):259-73. doi: 10.1016/j.neuron.2012.11.002.

Supplemental Content

Loading ...
Support Center