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American Journal of Medical Genetics. Part A|July 12, 2017
The phenotype of EZH2 haploinsufficiency-1.2-Mb deletion at 7q36.1 in a child with tall stature and intellectual disabilityTanay Suri, Abhijit DixitPractical Neurology|February 12, 2016
When the face says it all: dysmorphology in identifying syndromic causes of epilepsyAbhijit Dixit, Mohnish SuriPediatric Neurology|October 18, 2011
Neurologic presentation of triple A syndromeAbhijit Dixit, Gabriel Chow, Ajoy SarkarBreathe (Sheffield, England)|June 5, 2020
Clues beyond the lung: an unusual diagnosis in an infant with chronic lung diseaseRachel Walsh, Dushyant Batra, Abhijit Dixit, et al.American Journal of Medical Genetics. Part A|August 7, 2013
Two Somali half-siblings with CHST3-related chondrodysplasia illustrating the phenotypic spectrum and intrafamilial variabilityGeorge A Tanteles, Abhijit Dixit, Sunil Dhar, et al.Pediatric Nephrology (Berlin, Germany)|February 20, 2016
Renal failure from birth-AKI or CKD? QuestionsSean Carter, Abhijit Dixit, Andrew Lunn, et al.Clinical Kidney Journal|March 29, 2021
Joubert syndrome diagnosed renally lateElizabeth Collard, Catherine Byrne, Michalis Georgiou, et al.BMJ Case Reports|September 10, 2025
Renal tubular dysgenesis due to variants in the gene encoding ACE in a child surviving the neonatal periodJulia Sanpera-Iglesias, Martin Christian, Faezeh Sakhinia, et al.American Journal of Medical Genetics. Part A|March 18, 2026
Refinement of Connective Tissue Disorder Diagnosis From Marfan to Loeys-Dietz Syndrome Type 4-End of a 30-Year Diagnostic OdysseyNeel Kothari, Nora Shannon, Bara Erhayiem, et al.Journal of Assisted Reproduction and Genetics|August 13, 2013
Association of progesterone receptor gene polymorphism with male infertility and clinical outcome of ICSISanjukta Sen, Abhijit Dixit, Chitra Thakur, et al.Pageof 4