Lynda Pollack
Orlando Health(US)Arnold Palmer Hospital for Children(US)
Publications by Year
Research Areas
Genomics and Rare Diseases, Wnt/β-catenin signaling in development and cancer, Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders, Genomics and Chromatin Dynamics
Most-Cited Works
- → POGZ truncating alleles cause syndromic intellectual disability(2016)106 cited
- → Sporadic occurrence of Duchenne Muscular Dystrophy: evidence for new mutation(1980)44 cited
- → Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variability(2021)36 cited
- → Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice(2023)17 cited
- → Additional de novo missense genetic variants in NALCN associated with CLIFAHDD syndrome(2017)16 cited
- → Thrombosis in a Pregnant Hemophilia A Carrier After Intrapartum Recombinant Factor VIII(2005)13 cited
- → De novo duplication of the 7q11 leads to q22 region.(1983)9 cited
- → Further delineation of Basel‐Vanagaite‐Smirin‐Yosef syndrome: Report of three patients(2020)9 cited
- → 1012 TRANSIENT HYPERAMMONEMIA IN TERM AND PRETERM INFANTS(1978)6 cited
- Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome : WNT signaling perturbation and phenotypic variability(2022)