| " Developmental brain dysfunction: Revival and expansion of old concepts based on new genetic evidence": Corrections. A Moreno-De-Luca, SM Myers, TD Challman, D Moreno-De-Luca, ... Elsevier Science, 2013 | | 2013 |
| Autism spectrum disorders SM Myers, TD Challman, American Academy of Pediatrics Developmental and Behavioral Pediatrics, 249-291, 2011 | 24 | 2011 |
| Congenital heart defects associated with Smith-Magenis syndrome: two cases of total anomalous pulmonary venous return SM Myers, TD Challman American journal of medical genetics 131 (1), 99-100, 2004 | 18 | 2004 |
| Creating a Standardized, Online Screening Assessment for Detecting Early Childhood Delays M Brown, H Fisher, CM Taylor, LK Walsh, TD Challman, N Eisenhauer | | |
| De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females EE Palmer, T Stuhlmann, S Weinert, E Haan, H Van Esch, M Holvoet, ... Molecular psychiatry 23 (2), 222-230, 2018 | 63 | 2018 |
| Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence A Moreno-De-Luca, SM Myers, TD Challman, D Moreno-De-Luca, ... The Lancet Neurology 12 (4), 406-414, 2013 | 353 | 2013 |
| End‐stage renal failure in Smith–Magenis syndrome SM Myers, TD Challman, GH Bock American Journal of Medical Genetics Part A 143 (16), 1922-1924, 2007 | 7 | 2007 |
| GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder C Shieh, N Jones, B Vanle, M Au, AY Huang, APG Silva, H Lee, ... Genetics in Medicine, 1-11, 2020 | 29 | 2020 |
| In addition to the Editor, Associate Editors, and Editorial Board, other experts and scholars are often asked to help review manuscripts submitted to the Journal. The Editor … R Accordino, LW Ada, MT Acosta, WH Ahearn, N Akshoomoff, B Albrecht, ... J Autism Dev Disord 39, 688-691, 2009 | | 2009 |
| Insufficient Evidence for “Autism-Specific” Genes SM Myers, TD Challman, R Bernier, T Bourgeron, WK Chung, ... OSF Preprints, 2020 | 145 | 2020 |
| Methylphenidate: its pharmacology and uses TD Challman, JJ Lipsky Mayo Clinic Proceedings 75 (7), 711-721, 2000 | 478 | 2000 |
| Pain insensitivity: distal S6-segment mutations in NaV1.9 emerge as critical hotspot MK King, E Leipold, JM Goehringer, I Kurth, TD Challman neurogenetics 18 (3), 179-181, 2017 | 25 | 2017 |
| Proximal 6q interstitial deletion without mental retardation SM Myers, TD Challman PEDIATRIC RESEARCH 55 (4), 277A-277A, 2004 | | 2004 |
| Proximal 6q interstitial deletion without severe mental retardation. SM Myers, TD Challman Genetic counseling (Geneva, Switzerland) 16 (3), 269-276, 2005 | 4 | 2005 |
| SHARED GENOMIC CONTRIBUTORS TO DEVELOPMENTAL AND NEUROPSYCHIATRIC DISORDERS C Martin, B Finucane, CM Taylor, TD Challman, AM De Luca, K Wain, ... European Neuropsychopharmacology 29, S20-S21, 2019 | | 2019 |
| Shift happens: family background influences clinical variability in genetic neurodevelopmental disorders B Finucane, TD Challman, CL Martin, DH Ledbetter GeneticS in medicine 18 (4), 302-304, 2016 | 48 | 2016 |
| The Editors wish to acknowledge with thanks the advice and critical reviews provided by the following consulting editors: Lynn Adams W Ahearn, M Alessandri, M Aman, C Ames, G Anderson, V Anderson, ... J Autism Dev Disord 36, 1149-1153, 2006 | | 2006 |
| The Medical Evaluation of Children with Pervasive Developmental Disorders TD Challman, SK Katusic, WJ Barbaresi Journal of Developmental & Behavioral Pediatrics 20 (5), 400, 1999 | | 1999 |
| The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11. 2 deletions A Moreno-De-Luca, DW Evans, KB Boomer, E Hanson, R Bernier, ... JAMA psychiatry 72 (2), 119-126, 2015 | 140 | 2015 |
| The value of genomic variant ClinVar submissions from clinical providers: Beyond the addition of novel variants KE Wain, E Palen, JM Savatt, D Shuman, B Finucane, A Seeley, ... Human mutation 39 (11), 1660-1667, 2018 | 14 | 2018 |
