Andrew Lane

Paternal Uniparental Isodisomy of Chromosome 20q—and the Resulting Changes in GNAS1 Methylation—as a Plausible Cause of Pseudohypoparathyroidism

Murat Bastepe, Andrew Lane, Harald Jüppner · The American Journal of Human Genetics · 2001 · 202 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Mutations in CEP57 cause mosaic variegated aneuploidy syndrome

Katie Snape, Sandra Hanks, Elise Ruark et al. · Nature Genetics · 2011 · 169 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia

Claus‐Eric Ott, Gundula Leschik, Fabienne Trotier et al. · Human Mutation · 2010 · 70 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Celiac Disease in Children, Adolescents, and Young Adults with Autoimmune Thyroid Disease

Nadia Sattar, Farrah Lazare, Martina Kacer et al. · The Journal of Pediatrics · 2010 · 67 citations

Medicine, Endocrinology, Immunology +16

Neurocognitive function in children with compensated hypothyroidism: lack of short term effects on or off thyroxin

Naghma J. Aijaz, Evelyn M Flaherty, Thomas Preston et al. · BMC Endocrine Disorders · 2006 · 49 citations · Full text

Medicine, Child Health, Endocrinology +17