Sangeetha Mahadevan

Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader–Willi syndrome

Angela L. Duker, Blake C. Ballif, Erawati V. Bawle et al. · European Journal of Human Genetics · 2010 · 316 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +9

Repeat Organ Transplantation in the United States, 1996–2005

John C. Magee, Mark L. Barr, Giacomo Basadonna et al. · American Journal of Transplantation · 2007 · 210 citations · Full text

Factors associated with mental health outcomes across healthcare settings in Oman during COVID-19: frontline versus non-frontline healthcare workers

Muna Alshekaili, Walid Hassan, Nazik Al Said et al. · BMJ Open · 2020 · 178 citations · Full text

Sleep Disorders, Quality Of Life, Healthcare Settings +25

Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological?

Przemysław Szafrański, Christian P. Schaaf, Richard Person et al. · Human Mutation · 2010 · 141 citations

Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles

Ngoc Minh Nguyen, Zhao‐Jia Ge, Ramesh Reddy et al. · The American Journal of Human Genetics · 2018 · 111 citations · Full text