Andrew H. Lane, MD

Dr. Lane is an expert in pediatric endocrine disorders, with experience treating diabetes, concerns about height growth, early or late puberty, underactive or overactive thyroid glands, calcium and mineral disorders, and other disorders. Since 1999 he has practiced at Stony Brook University, during which time he has also trained numerous students, residents, and fellows.  He has a lifelong dedication to applying the latest in evidence-based medicine to the health and well-being of pediatric patients and their caregivers, from birth through young adulthood.

Outcome of Isolated Premature Menarche: A Retrospective and Follow-Up Study. Ejaz S, Lane A, Wilson T;  Hormone research in paediatrics, 2015

Effect of pioglitazone on the course of new-onset type 1 diabetes mellitus. Tafuri KS, Godil MA, Lane AH, Wilson TA; Journal of clinical research in pediatric endocrinology, 2013

Erroneous prenatal diagnosis of congenital adrenal hyperplasia owing to a duplication of the CYP21A2 gene. Lekarev O, Tafuri K, Lane AH, Zhu G., Nakamoto JM, Buller-Burckle AM, Wilson TA, New MI; Journal of perinatology: official journal of the California Perinatal Association, 2013 Jan

Celiac disease in children, adolescents, and young adults with autoimmune thyroid disease. Sattar N, Lazare F, Kacer M, Aguayo-Figueroa L, Desikan V, Garcia M, Lane A, Chawla A, Wilson T; The Journal of pediatrics, 2011 Feb

Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia. Ott CE, Leschik G, Trotier F, Brueton L, Brunner HG, Brussel W, Guillen-Navarro E, Haase C, Kohlhase J, Kotzot D, Lane A, Lee-Kirsch MA, Morlot S, Simon ME, Steichen-Gersdorf E, Tegay DH, Peters H, Mundlos S, Klopocki E; Human mutation, 2010 Aug

The effect of oral leucine on protein metabolism in adolescents with type 1 diabetes mellitus. Desikan V, Mileva I, Garlick J, Lane AH, Wilson TA, McNurlan MA; International journal of pediatric endocrinology, 2010

Effect of inspiration/expiration on height measurement. Kacer M, Zhang G, Lane AH, Chen JJ, Wilson TA; Journal of pediatric endocrinology & metabolism : JPEM, 2008 Aug

Glucose metabolism and insulin secretion in a patient with ABCC8 mutation and Fanconi-Bickel syndrome caused by maternal isodisomy of chromosome 3. Hoffman TL, Blanco E, Lane A, Galvin-Parton P, Gadi I, Santer R, DeLeon D, Stanley C, Wilson TA; Clinical genetics, 2007 Jun

Accuracy of self-reported height measurements in parents and its effect on mid-parental target height calculation. Braziuniene I, Wilson TA, Lane AH; BMC endocrine disorders, 2007

Contiguous gene deletion involving L1CAM and AVPR2 causes X-linked hydrocephalus with nephrogenic diabetes insipidus. Tegay DH, Lane AH, Roohi J, Hatchwell E; American journal of medical genetics. Part A, 2007 Mar 15

Use of subcutaneous DDAVP in infants with central diabetes insipidus. Blanco EJ, Lane AH, Aijaz N, Blumberg D, Wilson TA; Journal of pediatric endocrinology & metabolism : JPEM, 2006 Jul

Neurocognitive function in children with compensated hypothyroidism: lack of short term effects on or off thyroxin. Aijaz NJ, Flaherty EM, Preston T, Bracken SS, Lane AH, Wilson TA; BMC endocrine disorders, 2006

Thyrotoxic periodic paralysis associated with a mutation in the sodium channel gene SCN4A. Lane AH, Markarian K, Braziunene I; Journal of pediatric endocrinology & metabolism : JPEM,2004 Dec

Type 1 diabetes mellitus masked by primary adrenal insufficiency in a child with autoimmune polyglandular syndrome type 2. Aijaz NJ, Blanco E, Lane AH, Wilson TA; Clinical pediatrics, 2003 Jan-Feb

Mosaic variegated aneuploidy with growth hormone deficiency and congenital heart defects. Lane AH, Aijaz N, Galvin-Parton P, Lanman J, Mangano R, Wilson TA; American journal of medical genetics, 2002 Jul 1

Paternal uniparental isodisomy of chromosome 20q--and the resulting changes in GNAS1 methylation--as a plausible cause of pseudohypoparathyroidism. Bastepe M, Lane AH, Juppner H; American journal of human genetics, 2001 May

Congenital nasal pyriform aperture stenosis associated with central diabetes insipidus. Godil MA, Galvin-Parton P, Monte D, Zerah M, Purandare A, Lane AH, Wilson TA; The Journal of pediatrics, 2000 Aug

Endogenous expression of Mullerian inhibiting substance in early postnatal rat sertoli cells requires multiple steroidogenic factor-1 and GATA-4-binding sites. Watanabe K, Clarke TR, Lane AH, Wang X, Donahoe PK; Proceedings of the National Academy of Sciences of the United States of America, 2000 Feb 15

Diagnostic utility of Mullerian inhibiting substance determination in patients with primary and recurrent granulosa cell tumors. Lane AH, Lee MM, Fuller AF Jr, Kehas DJ, Donahoe PK, MacLaughlin DT; Gynecologic oncology, 1999 Apr

New insights into mullerian inhibiting substance and its mechanism of action. Lane AH, Donahoe PK; The Journal of endocrinology, 1998 Jul

Von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma. Seizinger BR, Rouleau GA, Ozelius LJ, Lane AH, Farmer GE, Lamiell JM, Haines J, Yuen JW, Collins D, Majoor-Krakauer D, et al.; Nature, 1988 Mar 17

DNA linkage analysis in Von Recklinghausen neurofibromatosis. Seizinger BR, Rouleau G, Lane AH, Ozelius LJ, Faryniarz AG, Iannazzi J, Hobbs W, Roy JC, Falcone B, Huson S, et al.; Journal of medical genetics,1987 Sep

Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene. Seizinger BR, Rouleau GA, Ozelius LJ, Lane AH, Faryniarz AG, Chao MV, Huson S, Korf BR, Parry DM, Pericak-Vance MA, et al.; Cell, 1987 Jun 5

Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosis. Seizinger BR, Rouleau G, Ozelius LJ, Lane AH, St George-Hyslop P, Huson S, Gusella JF, Martuza RL; Science (New York, N.Y.), 1987 Apr 17

Linkage analysis in von Recklinghausen neurofibromatosis (NF1) with DNA markers for chromosome 17. Seizinger BR, Rouleau GA, Lane AH, Farmer G, Ozelius LJ, Haines JL, Parry DM, Korf BR, Pericak-Vance MA, Faryniarz AG, et al.; Genomics, 1987 Dec