Ram Singh

Cytogenomic identification and long-read single molecule real-time (SMRT) sequencing of a Bardet–Biedl Syndrome 9 (BBS9) deletion

Wahab A. Khan, R. Sebra, E. Jabs, 2018, npj Genomic Medicine.

De Novo Interstitial Deletion of 9q in a Pediatric Patient With Global Developmental Delay

Ram Singh, N. Cohen, Dennis Keselman, 2019, Child neurology open.

Maternal uniparental disomy of chromosome 15 and concomitant STRC and CATSPER2 deletion‐mediated deafness‐infertility syndrome

Wahab A. Khan, S. Scott, Amy C Yang, 2017, American journal of medical genetics. Part A.

Haploinsufficiency of the basic helix–loop–helix transcription factor HAND2 causes congenital heart defects

Wahab A. Khan, S. Scott, L. Edelmann, 2020, American journal of medical genetics. Part A.

Cytogenomic identification and long-read single molecule real-time (SMRT) sequencing of a Bardet–Biedl Syndrome 9 (BBS9) deletion

Wahab A. Khan, R. Sebra, E. Jabs, 2018, npj Genomic Medicine.

Aberrations in folate metabolic pathway and altered susceptibility to autism

Usha Naik, R. Akella, Ram Singh, 2009, Psychiatric genetics.