Andrew Lane
Publications by Year
Research Areas
Sexual Differentiation and Disorders, Neonatal Respiratory Health Research, Growth Hormone and Insulin-like Growth Factors, Hyperglycemia and glycemic control in critically ill and hospitalized patients, Ovarian function and disorders
Most-Cited Works
- → Paternal Uniparental Isodisomy of Chromosome 20q—and the Resulting Changes in GNAS1 Methylation—as a Plausible Cause of Pseudohypoparathyroidism(2001)202 cited
- → Mutations in CEP57 cause mosaic variegated aneuploidy syndrome(2011)168 cited
- → Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia(2010)69 cited
- → Celiac Disease in Children, Adolescents, and Young Adults with Autoimmune Thyroid Disease(2010)67 cited
- → Neurocognitive function in children with compensated hypothyroidism: lack of short term effects on or off thyroxin(2006)49 cited
- → Use of Subcutaneous DDAVP in Infants with Central Diabetes Insipidus(2006)29 cited
- → Thyrotoxic Periodic Paralysis Associated with a Mutation in the Sodium Channel Gene SCN4A(2004)27 cited
- → Contiguous gene deletion involving L1CAM and AVPR2 causes X‐linked hydrocephalus with nephrogenic diabetes insipidus(2007)26 cited
- → Mosaic variegated aneuploidy with growth hormone deficiency and congenital heart defects(2002)26 cited
- → Erroneous prenatal diagnosis of congenital adrenal hyperplasia owing to a duplication of the CYP21A2 gene(2012)21 cited