Bidisha Saha

WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations

Katrin Friedrich, Lin Lee, Dru F. Leistritz et al. · Human Genetics · 2010 · 101 citations · Full text

Unusual Intronic Mutations, Somatic Variant, Mendelian Disorder +10

Potassium acts through mTOR to regulate its own secretion

Mads Vaarby Sørensen, Bidisha Saha, Iben Skov Jensen et al. · JCI Insight · 2019 · 70 citations · Full text

Coronary artery disease in a Werner syndrome‐like form of progeria characterized by low levels of progerin, a splice variant of lamin A

Fuki M. Hisama, Davor Lessel, Dru F. Leistritz et al. · American Journal of Medical Genetics Part A · 2011 · 67 citations · Full text

Werner Syndrome, Genetics, Splice Variant +16

Phosphorylation at distinct subcellular locations underlies specificity in mTORC2-mediated activation of SGK1 and Akt

Catherine E. Gleason, Juan A. Osés-Prieto, Kathy H. Li et al. · Journal of Cell Science · 2019 · 61 citations · Full text

<i>POLD1</i>Germline Mutations in Patients Initially Diagnosed with Werner Syndrome

Davor Lessel, Fuki M. Hisama, Katalin Szakszon et al. · Human Mutation · 2015 · 60 citations · Full text

Developmental Anomaly, Werner Syndrome, Developmental Biology +14