| CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum EDH Konrad, N Nardini, A Caliebe, I Nagel, D Young, G Horvath, ... Genetics in Medicine 21 (12), 2723-2733, 2019 | 62 | 2019 |
| Residential environmental tobacco smoke exposure during pregnancy and low birth weight of neonates: case control study in a public hospital in Lucknow, India D Khattar, S Awasthi, V Das Indian pediatrics 50, 134-138, 2013 | 45 | 2013 |
| Biochemistry, ammonia SS Mohiuddin, D Khattar | 34 | 2019 |
| Tachypnea SB Park, D Khattar Statpearls [Internet], 2024 | 25 | 2024 |
| Cystic kidney disease SY Goksu, D Khattar | 10* | 2020 |
| PI3K signaling specifies proximal-distal fate by driving a developmental gene regulatory network in SOX9+ mouse lung progenitors D Khattar, S Fernandes, J Snowball, M Guo, MC Gillen, SS Jain, D Sinner, ... Elife 11, e67954, 2022 | 9 | 2022 |
| Detection and impact of genetic disease in a level IV neonatal intensive care unit L Hagen, D Khattar, K Whitehead, H He, DT Swarr, K Suhrie Journal of Perinatology 42 (5), 580-588, 2022 | 9 | 2022 |
| Confirmatory testing illustrates additional risks for structural sex chromosome abnormalities in fetuses with a non‐invasive prenatal screen positive for monosomy X KL Sund, D Khattar, T Boomer, S Caldwell, L Dyer, RJ Hopkin, ... American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2020 | 8 | 2020 |
| CHARGE syndrome in the era of molecular diagnosis: similar outcomes in those without coloboma or choanal atresia BN Simpson, D Khattar, H Saal, CE Prada, D Choo, L Marcheschi, ... European Journal of Medical Genetics 64 (1), 104103, 2021 | 7 | 2021 |
| Study DDD, Sticht H, Gregor A, Van Esch H, Zweier C. CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum EDH Konrad, N Nardini, A Caliebe, I Nagel, D Young, G Horvath, ... Genet Med 21 (12), 2723-33, 2019 | 5 | 2019 |
| Characterization of the hepatosplenic and portal venous findings in patients with Proteus syndrome V Takyar, D Khattar, A Ling, R Patel, JC Sapp, SA Kim, S Auh, ... American Journal of Medical Genetics Part A 176 (12), 2677-2684, 2018 | 4 | 2018 |
| A deep intronic PKHD1 variant identified by SpliceAI in a deceased neonate with autosomal recessive polycystic kidney disease F Richter, KD Rutherford, AJ Cooke, M Meshkati, V Eddy-Abrams, ... American Journal of Kidney Diseases 83 (6), 829-833, 2024 | 3 | 2024 |
| Diabetic embryopathy. Treasure Island (FL) J Bhandari, PK Thada, D Khattar StatPearls Publishing, 2022 | 2 | 2022 |
| Esophageal atresia with or without tracheoesophageal fistula: comorbidities, genetic evaluations, and neonatal outcomes D Khattar, KR Suhrie Cureus 15 (2), 2023 | 1 | 2023 |
| P210: Esophageal atresia with or without tracheoesophageal fistula: Genetic evaluation and clinical outcomes D Khattar, K Suhrie Genetics in Medicine Open 1 (1), 2023 | | 2023 |
| Like Mother, Like Daughter: Feeding Intolerance in the NICU D Khattar, RJ Hopkin NeoReviews 22 (11), e774-e777, 2021 | | 2021 |
| PI3K Signaling Specifies Proximal-Distal Fate by Driving a Developmental Gene Regulatory Network in Sox9+ Lung Progenitors D Khattar, S Fernandes, J Snowball, M Guo, MC Gillen, D Sinner, ... bioRxiv, 2021.02. 26.433053, 2021 | | 2021 |
| FETAL MRI FINDINGS IN JOUBERT SYNDROME BN Simpson, J Owens, R Hopkin, B Kline-Fath, D Khattar, BR Sullivan, ... AMERICAN JOURNAL OF MEDICAL GENETICS PART A 182 (4), 893-893, 2020 | | 2020 |
| CTCF variants in 31 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum EDH Konrad, N Nardini, M Blyth, K Prescott, AM Bouman, EH Brilstra, ... European Journal Of Human Genetics 27, 1116-1117, 2019 | | 2019 |
| Epigenomic Analysis of Sox9+ Lung Epithelial Progenitor Cell Specification Defines New Transcriptional Regulatory Networks in Lung Development DT Swarr, S Fernandes, D Khattar, W Zacharias, M Gillen B95. CELLULAR AND MOLECULAR LANDSCAPE OF THE LUNG, A4009-A4009, 2019 | | 2019 |
