| Year |
Citation |
Score |
| 2022 |
Butler MG, Moreno-De-Luca D, Persico AM. Actionable Genomics in Clinical Practice: Paradigmatic Case Reports of Clinical and Therapeutic Strategies Based upon Genetic Testing. Genes. 13. PMID 35205368 DOI: 10.3390/genes13020323 |
0.452 |
|
| 2021 |
Moreno-De-Luca D, Martin CL. All for one and one for all: heterogeneity of genetic etiologies in neurodevelopmental psychiatric disorders. Current Opinion in Genetics & Development. 68: 71-78. PMID 33773394 DOI: 10.1016/j.gde.2021.02.015 |
0.462 |
|
| 2020 |
Moreno-De-Luca D, Kavanaugh BC, Best CR, Sheinkopf SJ, Phornphutkul C, Morrow EM. Clinical Genetic Testing in Autism Spectrum Disorder in a Large Community-Based Population Sample. Jama Psychiatry. PMID 32401282 DOI: 10.1001/Jamapsychiatry.2020.0950 |
0.727 |
|
| 2019 |
Montplaisir R, Lee E, Moreno-De-Luca D, Myers WC. Mosaic trisomy 20 and mitigation in capital crimes sentencing: A review and case report. Behavioral Sciences & the Law. PMID 31389076 DOI: 10.1002/bsl.2422 |
0.325 |
|
| 2019 |
Besterman AD, Moreno-De-Luca D, Nurnberger JI. 21st-Century Genetics in Psychiatric Residency Training: How Do We Get There? Jama Psychiatry. PMID 30601877 DOI: 10.1001/Jamapsychiatry.2018.3872 |
0.356 |
|
| 2018 |
Nurnberger JI, Austin J, Berrettini WH, Besterman AD, DeLisi LE, Grice DE, Kennedy JL, Moreno-De-Luca D, Potash JB, Ross DA, Schulze TG, Zai G. What Should a Psychiatrist Know About Genetics? Review and Recommendations From the Residency Education Committee of the International Society of Psychiatric Genetics. The Journal of Clinical Psychiatry. 80. PMID 30549495 DOI: 10.4088/Jcp.17Nr12046 |
0.487 |
|
| 2018 |
Moreno-De-Luca D, Ross ME, Ross DA. Leveraging the Power of Genetics to Bring Precision Medicine to Psychiatry: Too Little of a Good Thing? Biological Psychiatry. 83: e45-e46. PMID 29559097 DOI: 10.1016/J.Biopsych.2018.02.013 |
0.364 |
|
| 2017 |
Kishimoto K, Nomura J, Ellegood J, Fukumoto K, Lerch JP, Moreno-De-Luca D, Bourgeron T, Tamada K, Takumi T. Behavioral and neuroanatomical analyses in a genetic mouse model of 2q13 duplication. Genes to Cells : Devoted to Molecular & Cellular Mechanisms. PMID 28370817 DOI: 10.1111/Gtc.12487 |
0.328 |
|
| 2017 |
Vorstman JAS, Parr JR, Moreno-De-Luca D, Anney RJL, Nurnberger JI, Hallmayer JF. Autism genetics: opportunities and challenges for clinical translation. Nature Reviews. Genetics. 18: 362-376. PMID 28260791 DOI: 10.1038/Nrg.2017.4 |
0.509 |
|
| 2016 |
Moreno-De-Luca D. Beyond the Diagnosis: A Path Toward Understanding Behavior Through the Lens of Rare Genetics. Biological Psychiatry. 80: 92-3. PMID 27346082 DOI: 10.1016/J.Biopsych.2016.05.020 |
0.379 |
|
| 2015 |
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, Klei L, Mandell JD, ... Moreno-De-Luca D, et al. Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci. Neuron. 87: 1215-1233. PMID 26402605 DOI: 10.1016/J.Neuron.2015.09.016 |
0.732 |
|
| 2015 |
Turner TN, Sharma K, Oh EC, Liu YP, Collins RL, Sosa MX, Auer DR, Brand H, Sanders SJ, Moreno-De-Luca D, Pihur V, Plona T, Pike K, Soppet DR, Smith MW, et al. Loss of δ-catenin function in severe autism. Nature. 520: 51-6. PMID 25807484 DOI: 10.1038/Nature14186 |
0.497 |
|
| 2015 |
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, et al. A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity? Biological Psychiatry. 77: 775-84. PMID 25534755 DOI: 10.1016/J.Biopsych.2014.09.017 |
0.754 |
|
| 2015 |
Moreno-De-Luca A, Evans DW, Boomer KB, Hanson E, Bernier R, Goin-Kochel RP, Myers SM, Challman TD, Moreno-De-Luca D, Slane MM, Hare AE, Chung WK, Spiro JE, Faucett WA, Martin CL, et al. The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions. Jama Psychiatry. 72: 119-26. PMID 25493922 DOI: 10.1001/Jamapsychiatry.2014.2147 |
0.583 |
|
| 2014 |
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, et al. Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2. Autism Research : Official Journal of the International Society For Autism Research. 7: 355-62. PMID 24821083 DOI: 10.1002/Aur.1378 |
0.746 |
|
| 2014 |
Moreno-De-Luca D, Moreno-De-Luca A, Cubells JF, Sanders SJ. Cross-Disorder Comparison of Four Neuropsychiatric CNV Loci Current Genetic Medicine Reports. 2: 151-161. DOI: 10.1007/S40142-014-0045-7 |
0.561 |
|
| 2013 |
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, ... ... Moreno-De-Luca D, et al. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics. 45: 984-94. PMID 23933821 DOI: 10.1038/Ng.2711 |
0.718 |
|
| 2013 |
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, et al. Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait. Biological Psychiatry. 74: 576-84. PMID 23746936 DOI: 10.1016/J.Biopsych.2013.04.018 |
0.734 |
|
| 2013 |
Moreno-De-Luca A, Myers SM, Challman TD, Moreno-De-Luca D, Evans DW, Ledbetter DH. Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence. The Lancet. Neurology. 12: 406-14. PMID 23518333 DOI: 10.1016/S1474-4422(13)70011-5 |
0.672 |
|
| 2013 |
Moreno-De-Luca D, Sanders SJ, Willsey AJ, Mulle JG, Lowe JK, Geschwind DH, State MW, Martin CL, Ledbetter DH. Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts. Molecular Psychiatry. 18: 1090-5. PMID 23044707 DOI: 10.1038/Mp.2012.138 |
0.683 |
|
| 2012 |
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, Martin CL, et al. Common genetic variants, acting additively, are a major source of risk for autism. Molecular Autism. 3: 9. PMID 23067556 DOI: 10.1186/2040-2392-3-9 |
0.744 |
|
| 2011 |
Kaminsky EB, Kaul V, Paschall J, Church DM, Bunke B, Kunig D, Moreno-De-Luca D, Moreno-De-Luca A, Mulle JG, Warren ST, Richard G, Compton JG, Fuller AE, Gliem TJ, Huang S, et al. An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 13: 777-84. PMID 21844811 DOI: 10.1097/Gim.0B013E31822C79F9 |
0.591 |
|
| 2011 |
Sanders SJ, Ercan-Sencicek AG, Hus V, Luo R, Murtha MT, Moreno-De-Luca D, Chu SH, Moreau MP, Gupta AR, Thomson SA, Mason CE, Bilguvar K, Celestino-Soper PB, Choi M, Crawford EL, et al. Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron. 70: 863-85. PMID 21658581 DOI: 10.1016/J.Neuron.2011.05.002 |
0.735 |
|
| 2011 |
Moreno-De-Luca D, Cubells JF. Copy number variants: a new molecular frontier in clinical psychiatry. Current Psychiatry Reports. 13: 129-37. PMID 21253883 DOI: 10.1007/S11920-011-0183-5 |
0.536 |
|
| 2011 |
Moreno-De-Luca D, Mulle JG, Kaminsky EB, Sanders SJ, Myers SM, Adam MP, Pakula AT, Eisenhauer NJ, Uhas K, Weik L, Guy L, Care ME, Morel CF, Boni C, Salbert BA, et al. Erratum: Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia (The American Journal of Human Genetics (2010) 87 (618-630)) American Journal of Human Genetics. 88. DOI: 10.1016/J.Ajhg.2010.12.005 |
0.617 |
|
| 2010 |
Moreno-De-Luca D, Mulle JG, Kaminsky EB, Sanders SJ, Myers SM, Adam MP, Pakula AT, Eisenhauer NJ, Uhas K, Weik L, Guy L, Care ME, et al. Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia. American Journal of Human Genetics. 87: 618-30. PMID 21055719 DOI: 10.1016/J.Ajhg.2010.10.004 |
0.659 |
|
| 2010 |
Devillard F, Guinchat V, Moreno-De-Luca D, Tabet AC, Gruchy N, Guillem P, Nguyen Morel MA, Leporrier N, Leboyer M, Jouk PS, Lespinasse J, Betancur C. Paracentric inversion of chromosome 2 associated with cryptic duplication of 2q14 and deletion of 2q37 in a patient with autism. American Journal of Medical Genetics. Part A. 152: 2346-54. PMID 20684015 DOI: 10.1002/Ajmg.A.33601 |
0.361 |
|
| 2010 |
Delorme R, Moreno-De-Luca D, Gennetier A, Maier W, Chaste P, Mössner R, Grabe HJ, Ruhrmann S, Falkai P, Mouren MC, Leboyer M, Wagner M, Betancur C. Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder. Bmc Medical Genetics. 11: 100. PMID 20565924 DOI: 10.1186/1471-2350-11-100 |
0.435 |
|
| 2009 |
Depienne C, Moreno-De-Luca D, Heron D, Bouteiller D, Gennetier A, Delorme R, Chaste P, Siffroi JP, Chantot-Bastaraud S, Benyahia B, Trouillard O, Nygren G, Kopp S, Johansson M, Rastam M, et al. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders. Biological Psychiatry. 66: 349-59. PMID 19278672 DOI: 10.1016/J.Biopsych.2009.01.025 |
0.473 |
|
| 2009 |
Giegling I, Moreno-De-Luca D, Calati R, Hartmann AM, Möller HJ, De Ronchi D, Rujescu D, Serretti A. Tyrosine hydroxylase and DOPA decarboxylase gene variants in personality traits. Neuropsychobiology. 59: 23-7. PMID 19221445 DOI: 10.1159/000202826 |
0.338 |
|
| 2008 |
Gong X, Bacchelli E, Blasi F, Toma C, Betancur C, Chaste P, Delorme R, Durand CM, Fauchereau F, Botros HG, Leboyer M, Mouren-Simeoni MC, Nygren G, Anckarsäter H, Rastam M, ... ... Moreno-De-Luca D, et al. Analysis of X chromosome inactivation in autism spectrum disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 830-5. PMID 18361425 DOI: 10.1002/Ajmg.B.30688 |
0.438 |
|
| 2008 |
Giegling I, Moreno-De-Luca D, Rujescu D, Schneider B, Hartmann AM, Schnabel A, Maurer K, Möller HJ, Serretti A. Dopa decarboxylase and tyrosine hydroxylase gene variants in suicidal behavior. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 308-15. PMID 17948905 DOI: 10.1002/Ajmg.B.30599 |
0.322 |
|
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