Ari J. Wassner | Medical Services
Specialties
Programs & Services
Languages
- English
Ari J. Wassner | Education
Undergraduate School
Haverford College
2000, Haverford, PA
Medical School
Harvard Medical School
2005, Boston, MA
Residency
Pediatrics
Boston Combined Residency Program (BCRP)
2008, Boston, MA
Residency
Chief Resident
Boston Combined Residency Program (BCRP)
2009, Boston, MA
Fellowship
Pediatric Endocrinology
Boston Children's Hospital
2012, Boston, MA
Ari J. Wassner | Certifications
- American Board of Pediatrics (Endocrinology)
- American Board of Pediatrics (General)
Ari J. Wassner | Professional History
Dr. Ari Wassner is Medical Director of the Thyroid Center, Director of the Endocrinology Fellowship Training Program at Boston Children's Hospital, and Associate Professor of Pediatrics at Harvard Medical School. He earned his MD from Harvard Medical School and completed residency in Pediatrics and fellowship in Pediatric Endocrinology at Boston Children’s Hospital. Dr. Wassner is an international expert in pediatric thyroid disease, serving for the American Thyroid Association (ATA) Pediatric Thyroid Cancer Guidelines Task Force and the writing group of the American Academy of Pediatrics (AAP) congenital hypothyroidism guidelines.
Dr. Wassner’s primary clinical focus is on congenital hypothyroidism and thyroid neoplasia in children. Dr. Wassner is actively involved in education and received the 2017 Masland Award for Excellence in Teaching from Harvard Medical School. He also serves on the Boston Children’s Hospital Graduate Medical Committee and is a member of the Academy at Harvard Medical School. In addition to his involvement in resident and fellow education, he directs preclinical medical education in Endocrinology at Harvard Medical School.
Ari J. Wassner | Publications
Congenital Hypothyroidism: Screening and Management. Pediatrics. 2023 01 01; 151(1). View Congenital Hypothyroidism: Screening and Management. Abstract
Congenital Hypothyroidism: Screening and Management. Pediatrics. 2023 01 01; 151(1). View Congenital Hypothyroidism: Screening and Management. Abstract
Pediatric thyroid cancer: Recent developments. Best Pract Res Clin Endocrinol Metab. 2023 Jan; 37(1):101715. View Pediatric thyroid cancer: Recent developments. Abstract
Autoimmune Thyroiditis and Risk of Malignancy in Children with Thyroid Nodules. Thyroid. 2022 09; 32(9):1109-1117. View Autoimmune Thyroiditis and Risk of Malignancy in Children with Thyroid Nodules. Abstract
Investigations Into Obesity and the Risk of Malignant Disease in Pediatric Thyroid Nodules-Reply. JAMA Otolaryngol Head Neck Surg. 2022 08 01; 148(8):793-794. View Investigations Into Obesity and the Risk of Malignant Disease in Pediatric Thyroid Nodules-Reply. Abstract
Is Thyroid Monitoring Warranted in Infants and Young Children After Intravascular Administration of Iodine-Based Contrast Media? AJR Am J Roentgenol. 2023 01; 220(1):144-145. View Is Thyroid Monitoring Warranted in Infants and Young Children After Intravascular Administration of Iodine-Based Contrast Media? Abstract
Association Between Body Mass Index and Thyroid Cancer in Children With Thyroid Nodules. JAMA Otolaryngol Head Neck Surg. 2022 04 01; 148(4):375-377. View Association Between Body Mass Index and Thyroid Cancer in Children With Thyroid Nodules. Abstract
Thyroid Nodules in Children With Familial Adenomatous Polyposis. Am J Gastroenterol. 2022 07 01; 117(7):1166-1168. View Thyroid Nodules in Children With Familial Adenomatous Polyposis. Abstract
Germline pathogenic variants in cancer risk genes among patients with thyroid cancer and suspected predisposition. Cancer Med. 2022 04; 11(8):1745-1752. View Germline pathogenic variants in cancer risk genes among patients with thyroid cancer and suspected predisposition. Abstract
Subtype of atypia on cytology and risk of malignancy in pediatric thyroid nodules. Cancer Cytopathol. 2022 05; 130(5):330-335. View Subtype of atypia on cytology and risk of malignancy in pediatric thyroid nodules. Abstract
Belzutifan, a Potent HIF2a Inhibitor, in the Pacak-Zhuang Syndrome. N Engl J Med. 2021 11 25; 385(22):2059-2065. View Belzutifan, a Potent HIF2a Inhibitor, in the Pacak-Zhuang Syndrome. Abstract
Predictors of Bilateral Disease in Pediatric Differentiated Thyroid Cancer. J Clin Endocrinol Metab. 2021 09 27; 106(10):e4242-e4250. View Predictors of Bilateral Disease in Pediatric Differentiated Thyroid Cancer. Abstract
Clinical utility of sonographic features in indeterminate pediatric thyroid nodules. Eur J Endocrinol. 2021 May; 184(5):657-665. View Clinical utility of sonographic features in indeterminate pediatric thyroid nodules. Abstract
Re: "The Use of the Bethesda System for Reporting Thyroid Cytopathology in Pediatric Thyroid Nodules: A Meta-Analysis" by Vuong et al. Thyroid. 2021 09; 31(9):1441. View Re: "The Use of the Bethesda System for Reporting Thyroid Cytopathology in Pediatric Thyroid Nodules: A Meta-Analysis" by Vuong et al. Abstract
Relationship of Preoperative Thyroid Dysfunction to Clinical Outcomes in Pediatric Cardiac Surgery. J Clin Endocrinol Metab. 2021 04 23; 106(5):e2129-e2136. View Relationship of Preoperative Thyroid Dysfunction to Clinical Outcomes in Pediatric Cardiac Surgery. Abstract
Natural History of Thyroid Disease in Children with PTEN Hamartoma Tumor Syndrome. J Clin Endocrinol Metab. 2021 03 08; 106(3):e1121-e1130. View Natural History of Thyroid Disease in Children with PTEN Hamartoma Tumor Syndrome. Abstract
Risk Stratification in Pediatric Thyroid Cancer: Growing Evidence for Individualized Therapy. J Clin Endocrinol Metab. 2021 03 08; 106(3):e1471-e1472. View Risk Stratification in Pediatric Thyroid Cancer: Growing Evidence for Individualized Therapy. Abstract
Severity of Proteinuria Is Directly Associated With Risk of Hypothyroidism in Adults. J Clin Endocrinol Metab. 2021 01 23; 106(2):e757-e762. View Severity of Proteinuria Is Directly Associated With Risk of Hypothyroidism in Adults. Abstract
Severity of Proteinuria Is Directly Associated With Risk of Hypothyroidism in Adults. J Clin Endocrinol Metab. 2021 Jan 23; 106(2):e757-e762. View Severity of Proteinuria Is Directly Associated With Risk of Hypothyroidism in Adults. Abstract
Consensus statement by the American Association of Clinical Endocrinology (AACE) and the American Head and Neck Society Endocrine Surgery Section (AHNS-ES) on Pediatric Benign and Malignant Thyroid Surgery. Head Neck. 2021 04; 43(4):1027-1042. View Consensus statement by the American Association of Clinical Endocrinology (AACE) and the American Head and Neck Society Endocrine Surgery Section (AHNS-ES) on Pediatric Benign and Malignant Thyroid Surgery. Abstract
Graves' disease in a five-month-old boy with an unusual treatment course. J Pediatr Endocrinol Metab. 2021 Mar 26; 34(3):401-406. View Graves' disease in a five-month-old boy with an unusual treatment course. Abstract
Consensus Statement by the American Association of Clinical Endocrinology (AACE) and the American Head and Neck Society Endocrine Surgery Section (AHNS) on Pediatric Benign and Malignant Thyroid Surgery. Endocr Pract. 2021 Mar; 27(3):174-184. View Consensus Statement by the American Association of Clinical Endocrinology (AACE) and the American Head and Neck Society Endocrine Surgery Section (AHNS) on Pediatric Benign and Malignant Thyroid Surgery. Abstract
Undernutrition and Pubertal Timing in Female Survivors of Medulloblastoma and Other Embryonal Tumors. J Clin Endocrinol Metab. 2020 10 01; 105(10). View Undernutrition and Pubertal Timing in Female Survivors of Medulloblastoma and Other Embryonal Tumors. Abstract
Unraveling the Genetics of Congenital Hypothyroidism: Challenges and Opportunities. J Clin Endocrinol Metab. 2020 09 01; 105(9). View Unraveling the Genetics of Congenital Hypothyroidism: Challenges and Opportunities. Abstract
MCT8 deficiency: collaborative rare disease phenotyping for care and research. Lancet Diabetes Endocrinol. 2020 07; 8(7):555-557. View MCT8 deficiency: collaborative rare disease phenotyping for care and research. Abstract
Update on congenital hypothyroidism. Curr Opin Endocrinol Diabetes Obes. 2020 02; 27(1):63-69. View Update on congenital hypothyroidism. Abstract
Assessment of American College of Radiology Thyroid Imaging Reporting and Data System (TI-RADS) for Pediatric Thyroid Nodules. Radiology. 2020 02; 294(2):415-420. View Assessment of American College of Radiology Thyroid Imaging Reporting and Data System (TI-RADS) for Pediatric Thyroid Nodules. Abstract
A Novel ALK Fusion in Pediatric Medullary Thyroid Carcinoma. Thyroid. 2019 11; 29(11):1704-1707. View A Novel ALK Fusion in Pediatric Medullary Thyroid Carcinoma. Abstract
COINCIDENT SUPPURATIVE THYROIDITIS AND GRAVES DISEASE IN A PATIENT WITH INFECTED BRANCHIAL CLEFT CYST. AACE Clin Case Rep. 2019 Nov-Dec; 5(6):e365-e368. View COINCIDENT SUPPURATIVE THYROIDITIS AND GRAVES DISEASE IN A PATIENT WITH INFECTED BRANCHIAL CLEFT CYST. Abstract
Differences in Thyroid Nodule Cytology and Malignancy Risk Between Children and Adults. Thyroid. 2019 08; 29(8):1097-1104. View Differences in Thyroid Nodule Cytology and Malignancy Risk Between Children and Adults. Abstract
Thyroid hormone therapy in congenital hypothyroidism and pediatric hypothyroidism. Endocrine. 2019 10; 66(1):51-62. View Thyroid hormone therapy in congenital hypothyroidism and pediatric hypothyroidism. Abstract
Natural History and Outcomes of Cytologically Benign Thyroid Nodules in Children. J Clin Endocrinol Metab. 2018 09 01; 103(9):3557-3565. View Natural History and Outcomes of Cytologically Benign Thyroid Nodules in Children. Abstract
Thyroid Nodules in Pediatric Patients: Sonographic Characteristics and Likelihood of Cancer. Radiology. 2018 08; 288(2):591-599. View Thyroid Nodules in Pediatric Patients: Sonographic Characteristics and Likelihood of Cancer. Abstract
Congenital Hypothyroidism. Clin Perinatol. 2018 03; 45(1):1-18. View Congenital Hypothyroidism. Abstract
Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis. Kidney Int. 2018 01; 93(1):204-213. View Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis. Abstract
Congenital hypothyroidism: insights into pathogenesis and treatment. Int J Pediatr Endocrinol. 2017; 2017:11. View Congenital hypothyroidism: insights into pathogenesis and treatment. Abstract
Prevalence and Significance of Thyroglobulin Antibodies in Pediatric Thyroid Cancer. J Clin Endocrinol Metab. 2017 09 01; 102(9):3146-3153. View Prevalence and Significance of Thyroglobulin Antibodies in Pediatric Thyroid Cancer. Abstract
Pediatric Hypothyroidism: Diagnosis and Treatment. Paediatr Drugs. 2017 Aug; 19(4):291-301. View Pediatric Hypothyroidism: Diagnosis and Treatment. Abstract
Myocardial Induction of Type 3 Deiodinase in Dilated Cardiomyopathy. Thyroid. 2017 05; 27(5):732-737. View Myocardial Induction of Type 3 Deiodinase in Dilated Cardiomyopathy. Abstract
Mutations in SLC26A1 Cause Nephrolithiasis. Am J Hum Genet. 2016 06 02; 98(6):1228-1234. View Mutations in SLC26A1 Cause Nephrolithiasis. Abstract
Liothyronine Improves Biochemical Control of Congenital Hypothyroidism in Patients with Central Resistance to Thyroid Hormone. J Pediatr. 2016 08; 175:167-172.e1. View Liothyronine Improves Biochemical Control of Congenital Hypothyroidism in Patients with Central Resistance to Thyroid Hormone. Abstract
Prevalence of Monogenic Causes in Pediatric Patients with Nephrolithiasis or Nephrocalcinosis. Clin J Am Soc Nephrol. 2016 Apr 07; 11(4):664-72. View Prevalence of Monogenic Causes in Pediatric Patients with Nephrolithiasis or Nephrocalcinosis. Abstract
Subclinical Hypothyroidism in Infancy: To Treat or Not to Treat, That Is the Question. J Pediatr. 2016 Mar; 170:17-9. View Subclinical Hypothyroidism in Infancy: To Treat or Not to Treat, That Is the Question. Abstract
Congenital hypothyroidism: recent advances. Curr Opin Endocrinol Diabetes Obes. 2015 Oct; 22(5):407-12. View Congenital hypothyroidism: recent advances. Abstract
Fourteen monogenic genes account for 15% of nephrolithiasis/nephrocalcinosis. J Am Soc Nephrol. 2015 Mar; 26(3):543-51. View Fourteen monogenic genes account for 15% of nephrolithiasis/nephrocalcinosis. Abstract
Mice with hepatocyte-specific deficiency of type 3 deiodinase have intact liver regeneration and accelerated recovery from nonthyroidal illness after toxin-induced hepatonecrosis. Endocrinology. 2014 Oct; 155(10):4061-8. View Mice with hepatocyte-specific deficiency of type 3 deiodinase have intact liver regeneration and accelerated recovery from nonthyroidal illness after toxin-induced hepatonecrosis. Abstract
Severe hypercalcaemia due to subcutaneous fat necrosis: presentation, management and complications. Arch Dis Child Fetal Neonatal Ed. 2014 Sep; 99(5):F419-21. View Severe hypercalcaemia due to subcutaneous fat necrosis: presentation, management and complications. Abstract
How are childhood thyroid nodules discovered: opportunities for improving early detection. J Pediatr. 2014 Mar; 164(3):658-60. View How are childhood thyroid nodules discovered: opportunities for improving early detection. Abstract
Rates of medical errors and preventable adverse events among hospitalized children following implementation of a resident handoff bundle. JAMA. 2013 Dec 04; 310(21):2262-70. View Rates of medical errors and preventable adverse events among hospitalized children following implementation of a resident handoff bundle. Abstract
Endocrine physiology in the newborn. Semin Pediatr Surg. 2013 Nov; 22(4):205-10. View Endocrine physiology in the newborn. Abstract
Hypothyroidism in the newborn period. Curr Opin Endocrinol Diabetes Obes. 2013 Oct; 20(5):449-54. View Hypothyroidism in the newborn period. Abstract
A standardized assessment of thyroid nodules in children confirms higher cancer prevalence than in adults. J Clin Endocrinol Metab. 2013 Aug; 98(8):3238-45. View A standardized assessment of thyroid nodules in children confirms higher cancer prevalence than in adults. Abstract
Isolated central hypothyroidism in young siblings as a manifestation of PROP1 deficiency: clinical impact of whole exome sequencing. Horm Res Paediatr. 2013; 79(6):379-86. View Isolated central hypothyroidism in young siblings as a manifestation of PROP1 deficiency: clinical impact of whole exome sequencing. Abstract
Synthesis and ion conductance behavior of a tetrameric alamethicin ion channel. Org Lett. 2002 May 16; 4(10):1647-9. View Synthesis and ion conductance behavior of a tetrameric alamethicin ion channel. Abstract