| Genes controlling affiliative behavior as candidate genes for autism CM Yrigollen, SS Han, A Kochetkova, T Babitz, JT Chang, FR Volkmar, ... Biological psychiatry 63 (10), 911-916, 2008 | 225 | 2008 |
| AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome CM Yrigollen, B Durbin-Johnson, L Gane, DL Nelson, R Hagerman, ... Genetics in Medicine 14 (8), 729-736, 2012 | 190 | 2012 |
| Macrophage migration inhibitory factor and autism spectrum disorders EL Grigorenko, SS Han, CM Yrigollen, L Leng, Y Mizue, GM Anderson, ... Pediatrics 122 (2), e438-e445, 2008 | 148 | 2008 |
| Fragile X AGG analysis provides new risk predictions for 45–69 repeat alleles SL Nolin, S Sah, A Glicksman, SL Sherman, E Allen, E Berry‐Kravis, ... American Journal of Medical Genetics Part A 161 (4), 771-778, 2013 | 139 | 2013 |
| Association between polymorphisms in the dopamine transporter gene and depression: evidence for a gene-environment interaction in a sample of juvenile detainees GJ Haeffel, M Getchell, RA Koposov, CM Yrigollen, CG De Young, ... Psychological science 19 (1), 62-69, 2008 | 134 | 2008 |
| AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission CM Yrigollen, L Martorell, B Durbin-Johnson, M Naudo, J Genoves, ... Journal of neurodevelopmental disorders 6 (1), 1-12, 2014 | 117 | 2014 |
| Clinical and molecular implications of mosaicism in FMR1 full mutations D Pretto, CM Yrigollen, HT Tang, J Williamson, G Espinal, CK Iwahashi, ... Frontiers in genetics 5, 318, 2014 | 110 | 2014 |
| Comparison of whole-genome DNA methylation patterns in whole blood, saliva, and lymphoblastoid cell lines TM Thompson, D Sharfi, M Lee, CM Yrigollen, OY Naumova, ... Behavior genetics 43 (2), 168-176, 2013 | 83 | 2013 |
| Aggressive behavior, related conduct problems, and variation in genes affecting dopamine turnover EL Grigorenko, CG DeYoung, M Eastman, M Getchell, GJ Haeffel, ... Aggressive Behavior: Official Journal of the International Society for …, 2010 | 79 | 2010 |
| Variation in the catechol-O-methyltransferase Val158Met polymorphism associated with conduct disorder and ADHD symptoms among adolescent male delinquents CG DeYoung, M Getchell, RA Koposov, CM Yrigollen, GJ Haeffel, ... Psychiatric genetics 20 (1), 20, 2010 | 76 | 2010 |
| Toxicity after AAV delivery of RNAi expression constructs into nonhuman primate brain MS Keiser, PT Ranum, CM Yrigollen, EM Carrell, GR Smith, AL Muehlmatt, ... Nature medicine 27 (11), 1982-1989, 2021 | 49 | 2021 |
| The COMT Val/Met polymorphism is associated with reading‐related skills and consistent patterns of functional neural activation N Landi, SJ Frost, WE Mencl, JL Preston, LK Jacobsen, M Lee, ... Developmental science 16 (1), 13-23, 2013 | 48 | 2013 |
| Genome-wide association and exome sequencing study of language disorder in an isolated population SA Kornilov, N Rakhlin, R Koposov, M Lee, C Yrigollen, AO Caglayan, ... Pediatrics 137 (4), 2016 | 45 | 2016 |
| Screening newborn blood spots for 22q11. 2 deletion syndrome using multiplex droplet digital PCR D Pretto, D Maar, CM Yrigollen, J Regan, F Tassone Clinical chemistry 61 (1), 182-190, 2015 | 41 | 2015 |
| Differential increases of specific FMR1 mRNA isoforms in premutation carriers DI Pretto, JS Eid, CM Yrigollen, HT Tang, EW Loomis, C Raske, ... Journal of medical genetics 52 (1), 42-52, 2015 | 39 | 2015 |
| Twenty-one-base-pair insertion polymorphism creates an enhancer element and potentiates SLC6A1 GABA transporter promoter activity R Hirunsatit, ED George, BK Lipska, HM Elwafi, L Sander, CM Yrigollen, ... Pharmacogenetics and genomics 19 (1), 53-65, 2009 | 35 | 2009 |
| Molecular biomarkers predictive of sertraline treatment response in young children with fragile X syndrome RR AlOlaby, SR Sweha, M Silva, B Durbin-Johnson, CM Yrigollen, ... Brain and Development 39 (6), 483-492, 2017 | 34 | 2017 |
| The Role of AGG Interruptions in the Transcription of FMR1 Premutation Alleles CM Yrigollen, F Tassone, B Durbin-Johnson, F Tassone PloS one 6 (7), e21728, 2011 | 30 | 2011 |
| Distribution of AGG interruption patterns within nine world populations CM Yrigollen, S Sweha, B Durbin-Johnson, L Zhou, E Berry-Kravis, ... Intractable & rare diseases research 3 (4), 153-161, 2014 | 27 | 2014 |
| A balanced t (10; 15) translocation in a male patient with developmental language disorder AG Ercan-Sencicek, NRD Wright, SJ Sanders, N Oakman, L Valdes, ... European journal of medical genetics 55 (2), 128-131, 2012 | 27 | 2012 |
