S. Mohan

Clinical validity assessment of genes frequently tested on intellectual disability/autism sequencing panels.

Tam P. Sneddon, Andrew R. Grant, C. Betancur, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

How I curate: applying American Society of Hematology-Clinical Genome Resource Myeloid Malignancy Variant Curation Expert Panel rules for RUNX1 variant curation for germline predisposition to myeloid malignancies

D. Pineda-Alvarez, David Wu, C. Kesserwan, 2020, Haematologica.

ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants.

Ying Wang, Christopher C. Porter, Anna L. Brown, 2019, Blood advances.

A Challenging Case of Domestically Acquired Leprosy in the Southern United States

J. Fairley, S. Mohan, S. Mohan, 2020, Open forum infectious diseases.

Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel.

Kristy Lee, Minjie Luo, P. Bray, 2021, Blood advances.

Subtelomeric rearrangements in Indian children with idiopathic intellectual disability/developmental delay: Frequency estimation & clinical correlation using fluorescence in situ hybridization (FISH)

S. Nampoothiri, Latha Ravichandran, S. Paul, 2016, The Indian journal of medical research.

The Impact of Toxic Language on the Health of Reddit Communities

Apala Guha, Fred Popowich, Michael Harris, 2017, Canadian Conference on AI.

Glanzmann thrombasthenia: Genetic basis and clinical correlates

Kristy Lee, Minjie Luo, P. Bray, 2020 .

Reciprocal Microduplication of the Williams-Beuren Syndrome Chromosome Region in a 9-Year-Old Omani Boy.

S. Nampoothiri, T. Koshy, Vettriselvi Venkatesan, 2016, Laboratory medicine.