Lauren Roth, M.D., is board certified in obstetrics and gynecology and reproductive endocrinology and infertility. She has published research on a range of fertility topics including polycystic ovary syndrome (PCOS) and the impact of weight on reproductive hormones. Dr. Roth sees patients in SGF’s Frederick, Rockville, and Silver Spring, Maryland offices. Lauren Roth, M.D. completed her undergraduate degree in Women’s Studies at the University of Maryland, College Park, where she graduated magna cum laude and inducted into Phi Beta Kappa. She earned her Medical Degree from the University of Maryland, Baltimore. She continued on to the University of Colorado, Denver where she completed her residency in Obstetrics and Gynecology and a 3 years fellowship in Reproductive Endocrinology and Infertility. She then served as an Assistant Professor at University of Colorado for 2 years before moving back to Maryland. Dr. Roth is board certified in both Obstetrics and Gynecology and Reproductive Endocrinology and Infertility. During her residency, Dr. Roth received several teaching awards and served as chief resident. During her fellowship and time as faculty at University of Colorado, she presented research at multiple national meetings and received three national research awards. She has published research on a range of fertility topics including polycystic ovary syndrome (PCOS) and the impact of weight on reproductive hormones. Dr. Roth joined the practice in 2015. Dr. Roth is rated as an Experienced provider by MediFind in the treatment of Turner Syndrome. Her top areas of expertise are Infertility, Asherman Syndrome, Sertoli Cell-Only Syndrome, and Tubal Disease.

Maximilian Muenke is a Medical Genetics provider in Bethesda, Maryland. Dr. Muenke is rated as a Distinguished provider by MediFind in the treatment of Turner Syndrome. His top areas of expertise are Holoprosencephaly, Turner Syndrome, Craniosynostosis, and Corpus Callosum Agenesis.

Maria Menucci is an Endocrinologist in Camp Springs, Maryland. Dr. Menucci is rated as a Distinguished provider by MediFind in the treatment of Turner Syndrome. Her top areas of expertise are Mixed Gonadal Dysgenesis, Turner Syndrome, Perrault Syndrome, and Vitamin B12 Deficiency.

Dr. Aniket Sidhaye is an assistant professor of medicine and pediatrics at the Johns Hopkins University School of Medicine. His specific clinical interests are cystic fibrosis related endocrine disorders, type 1 diabetes mellitus particularly emerging adults with diabetes, thyroid disorders, metabolic bone disease, and management of hospitalized persons with diabetes. Dr. Sidhaye earned his M.D. from Northwestern University’s Feinberg School of Medicine. He completed his residency at Northwestern University. He performed a research fellowship in endocrinology and metabolism at Northwestern University and also performed fellowships in endocrinology and metabolism at Johns Hopkins. His research interests include CF related diabetes, bone health of CF patients after lung transplant, and the care of emerging adults with type 1 diabetes. In addition, he is a committed educator serving as an advisor in the medical school, co-director for the endocrine course for pre-clinical medical students, and program director for our endocrine fellowship. Dr. Sidhaye is rated as an Experienced provider by MediFind in the treatment of Turner Syndrome. His top areas of expertise are Type B Insulin Resistance Syndrome, Type 1 Diabetes (T1D), Type 2 Diabetes (T2D), and Paget's Disease of Bone.

Sonja Rasmussen, MD, MS is Professor in the Department of Genetic Medicine at Johns Hopkins School of Medicine. She joined Johns Hopkins after 4 years at the University of Florida (UF) College of Medicine and College of Public Health and Health Professions where she served as a Professor in the Departments of Pediatrics, Epidemiology, and Obstetrics and Gynecology and as the Director of UF’s Precision Health Program. Before joining University of Florida in 2018, she served for 20 years at the Centers for Disease Control and Prevention (CDC) in Atlanta, where she held several scientific leadership roles. She served in leadership roles during several CDC responses to public health emergencies, including 2009 H1N1 influenza, H7N9 influenza, Middle East Respiratory Syndrome (MERS), and Zika virus. Dr. Rasmussen is an author on >300 peer-reviewed publications and is the lead editor of The CDC Field Epidemiology Manual, released by Oxford University Press in 2019. Her research interests focus on understanding the effects of infections and medications during pregnancy, genetic and environmental risk factors for birth defects, and morbidity and mortality associated with genetic conditions. Dr. Rasmussen is rated as an Experienced provider by MediFind in the treatment of Turner Syndrome. Her top areas of expertise are Microcephaly, Achalasia Microcephaly Syndrome, Gastroschisis, and Cortical Dysplasia.

Ambroise Wonkam is a Pediatrics specialist and a Medical Genetics provider in Baltimore, Maryland. Dr. Wonkam is rated as an Experienced provider by MediFind in the treatment of Turner Syndrome. His top areas of expertise are Anemia, Fragile X Syndrome, Pyle Disease, and Micrognathia.

Dr. Kristin M. Arcara completed her undergraduate studies at SUNY Buffalo, and received her medical degree from SUNY Upstate Medical University. She then completed her residency in pediatrics at the Johns Hopkins Hospital, spending an additional year serving as Chief Resident. She also completed a fellowship in pediatric endocrinology at the Johns Hopkins Hospital. Dr. Arcara has been a faculty member in the Division of Pediatric Endocrinology at Johns Hopkins since 2014. After her fellowship, Dr. Arcara spent one year as a Pediatric Endocrinologist at Children’s National Medical Center before returning to Johns Hopkins Hospital. Dr. Arcara’s clinical activities include heading a multidisciplinary Pediatric Diabetes clinic at Mt. Washington Pediatric Hospital, consisting of certified diabetes educators, registered dietitian and a team of psychologists with extensive training and expertise in the unique issues surrounding management of diabetes in children. She also has general pediatric endocrine clinics in which she evaluates and treats a variety of disorders including short stature, abnormal pubertal development, thyroid disorders, polycystic ovary syndrome, hypopituitarism, diabetes insipidus, pituitary adenoma, congenital adrenal hyperplasia and disorders of sexual differentiation, Turner syndrome and Prader Willi syndrome among others. Dr. Arcara is a member of Mt. Washington Pediatric Hospital’s multidisciplinary Prader Willi Syndrome clinic. Dr. Arcara is rated as an Experienced provider by MediFind in the treatment of Turner Syndrome. Her top areas of expertise are Type 1 Diabetes (T1D), Turner Syndrome, Mixed Gonadal Dysgenesis, and Short Stature (Growth Disorders).

Dr. Malinda Wu is a pediatric endocrinologist seeing patients at the Johns Hopkins Children’s Center in Baltimore, Maryland. She specializes in a wide range of pediatric endocrine conditions including metabolic bone disease, pediatric osteoporosis and cystic fibrosis endocrinopathies. Dr. Wu received her M.D. from Jefferson Medical College, Thomas Jefferson University. She completed pediatrics residency at Penn State Hershey Medical Center and her pediatric endocrine fellowship at Emory University School of Medicine. She received her Master of Science in Clinical Research from Emory University (2021). Dr. Wu has been a faculty member at Johns Hopkins since 2021. Dr. Wu’s research interests are in metabolic bone disease and the health of women with cystic fibrosis. Dr. Wu’s current research is focused on women with cystic fibrosis and how estrogen supplementation may impact their health. She has received grant funding from the Cystic Fibrosis Foundation. Dr. Wu is rated as an Experienced provider by MediFind in the treatment of Turner Syndrome. Her top areas of expertise are Osteogenesis Imperfecta, Hypogonadism, Malnutrition, Exocrine Pancreatic Insufficiency, and Hormone Replacement Therapy (HRT).

Anita Madison is an Obstetrics and Gynecologist in Lutherville, Maryland. Dr. Madison is rated as an Experienced provider by MediFind in the treatment of Turner Syndrome. Her top areas of expertise are Ectopic Pregnancy, Turner Syndrome, Mosaicism, Intersex, and Tubal Ligation.

Dr. William J. Ravekes is an associate professor of pediatrics at the Johns Hopkins University School of Medicine. A pediatric cardiologist, Dr. Ravekes serves as medical director of the Pediatric Heart Transplant and Mechanical Circulatory Support Program as well as pediatric cardiology fellowship director. He also specializes in non-invasive imaging, fetal echocardiography and the perioperative and intensive care of fetuses, infants, children and adults with congenital heart disease. Dr. Ravekes earned his medical degree at the George Washington University School of Medicine. He completed a pediatrics residency and chief residency at Lucile Salter Packard Children's Hospital at Stanford and a fellowship in pediatric cardiology at Boston Children’s Hospital. He served on the faculty of Texas Children’s Hospital prior to joining Johns Hopkins. His research interests include echocardiographic assessment of cardiac function, aortopathies, heart failure and transplantation, and medical education. He has published more than 90 scholarly articles. Dr. Ravekes is rated as an Experienced provider by MediFind in the treatment of Turner Syndrome. His top areas of expertise are Vascular Ehlers-Danlos Syndrome (VEDS), Pediatric Myocarditis, Ehlers-Danlos Syndrome (EDS), and Pulmonary Hypertension.

Dr. Couser obtained his bachelor’s degree from the University of Virginia and his Medical Doctorate from the Virginia Commonwealth University School of Medicine (VCU SOM). Dr. Couser’s ophthalmology residency was completed at Howard University where he served as co-chief resident in the last year of his residency. He received fellowship training in pediatric ophthalmology and adult strabismus at Emory University. Dr. Couser received a master’s degree in biotechnology from the Johns Hopkins University and completed a residency in clinical genetics at the University of North Carolina at Chapel Hill. He is one of only a few individuals currently board-certified by both the American Board of Ophthalmology and the American Board of Medical Genetics and Genomics. CV https://www.hopkinsmedicine.org/-/media/wilmer/documents/cvs/couser-cv Research Summary My primary research focus involves the identification and management of genetic eye diseases including rare inherited disorders affecting the eyes. Research and scholarly activities have been an integral component of my career path. I have been the principal investigator on 10 clinical trial/IRB studies and a co-investigator on others, participated with several committees or advisory panels related to research activities. I have been credited with over 120 book chapter, journal article and abstract publications. In addition, I served as the primary author/sole editor for a textbook titled Ophthalmic Genetic Diseases: A Quick Reference Guide to the Eye and External Ocular Adnexa Abnormalities, 1st Edition, published by Elsevier in 2018, which is one of only a few textbooks published in this subject area. I also served as a grant review panelist for the National Eye Institute Career Development Awards. Selected Publications *Couser NL, Masood MM, Strande NT, Foreman AKM, Crooks K, Weck KE, Lu M, Wilhelmsen KC, Roche M, Evans JP, Berg JS, Powell CM. 2015. The phenotype of multiple congenital anomalies- hypotonia-seizures syndrome 1: Report and review. Am J Med Genet Part A 9999A:1–6 *Couser NL, Lambert SR. Botulinum toxin: A treatment of consecutive esotropia in children. Strabismus 2012; 20(4):158-161 Couser NL, Lenhart PD, Hutchinson AK. Augmented Hummelsheim procedure to treat complete abducens nerve palsy. J AAPOS 2012;16(4):331-5 *Natario L. Couser, Maheer M. Masood, Arthur S. Aylsworth, and Roger E. Stevenson. Ocular manifestations in the X-linked intellectual disability syndromes. Ophthalmic Genet. 2017, Jan 23:1-12 *Couser NL, Brooks BP, Drack AV, Shankar SP. The evolving role of genetics in ophthalmology. Ophthalmic Genet. 2021 Jan 12:1-4. doi: 10.1080/13816810.2020.1868011. Dr. Couser is rated as an Experienced provider by MediFind in the treatment of Turner Syndrome. His top areas of expertise are Epicanthal Folds, Strabismus, Brown Syndrome, and Hypotonia.

Dr. David W. Cooke is an associate professor of pediatrics at the Johns Hopkins University School of Medicine. Dr. Cooke’s clinical activities include both a general pediatric endocrine clinic and a pediatric diabetes clinic. His clinical interests include all endocrine disorders in children and adolescents, including short stature, abnormal pubertal development, growth hormone dysregulation, thyroid disorders, hormone deficiencies, hypopituitarism, diabetes insipidis, pituitary adenoma, prolactinoma, goiter, Cushing's disease, Addison's disease, polycystic ovary syndrome, congenital adrenal hyperplasia and disorders of sexual differentiation, Turner syndrome and Klinefelter syndrome, among others. He serves as clinical director of the division of pediatric endocrinology and director of the Pediatric Endocrinology Fellowship Training Program at Johns Hopkins. He is a member of the Johns Hopkins Klinefelter Syndrome Center. Dr. Cooke completed his undergraduate studies at the Massachusetts Institute of Technology, and received his medical degree from the Duke University School of Medicine. He then completed his residency in pediatrics at The Johns Hopkins Hospital, where he also completed a fellowship in pediatric endocrinology. He has been a faculty member in the Division of Pediatric Endocrinology at the Johns Hopkins since 1993. After his fellowship, Dr. Cooke spent five years of additional research training in the Department of Biological Chemistry at Johns Hopkins, supported by an individual Physician Scientist Award from the National Institutes of Health (NIH). Dr. Cooke’s past research interest was the molecular basis of insulin resistance and obesity, with studies examining the role the adipocyte plays in these conditions. He had received research funding for these studies from the NIH and from the American Diabetes Association. Dr. Cooke is a recipient of the Johns Hopkins University School of Medicine Institute for Excellence in Education award for Outstanding Achievement in Medical and Biomedical Education. He also has been recognized as a Top Doctor by Baltimore magazine. Dr. Cooke is a member of the Society for Pediatric Research, the American Diabetes Association, the Endocrine Society and Pediatric Endocrinology Society. He is a fellow of the American Academy of Pediatrics. Dr. Cooke is rated as an Experienced provider by MediFind in the treatment of Turner Syndrome. His top areas of expertise are Klinefelter Syndrome, Type 1 Diabetes (T1D), Precocious Puberty, and Diabetic Ketoacidosis.

Sudhir Vashist is a Pediatric Cardiologist in Baltimore, Maryland. Dr. Vashist is rated as an Experienced provider by MediFind in the treatment of Turner Syndrome. His top areas of expertise are Wolff-Parkinson-White Syndrome, Myocarditis, Ventricular Septal Defects, and Atrioventricular Nodal Reentrant Tachycardia (AVNRT).

Nicholas Pietris is a Pediatric Cardiologist in Baltimore,, Maryland. Dr. Pietris is rated as an Experienced provider by MediFind in the treatment of Turner Syndrome. His top areas of expertise are Patent Ductus Arteriosus, Atrial Septal Defect (ASD), Patent Foramen Ovale, and Ventricular Septal Defects.

Peter Gaskin is a Pediatric Cardiologist in Baltimore, Maryland. Dr. Gaskin is rated as an Experienced provider by MediFind in the treatment of Turner Syndrome. His top areas of expertise are Patent Ductus Arteriosus, Heart Murmurs, Ventricular Septal Defects, and Bicuspid Aortic Valve.

Wendy Wong is a primary care provider, practicing in Family Medicine in Rockville, Maryland. Dr. Wong is rated as an Advanced provider by MediFind in the treatment of Turner Syndrome. Her top areas of expertise are Mixed Gonadal Dysgenesis, Turner Syndrome, Perrault Syndrome, Familial Combined Hyperlipidemia, and Hip Replacement. Dr. Wong is currently accepting new patients.

Neha Vyas is a Pediatric Endocrinologist in Baltimore, Maryland. Dr. Vyas is rated as an Advanced provider by MediFind in the treatment of Turner Syndrome. Her top areas of expertise are Type 1 Diabetes (T1D), Short Stature (Growth Disorders), Precocious Puberty, and Familial Short Stature (FSS).

Micah Hill is a Reproductive Medicine specialist and an Obstetrics and Gynecologist in Rockville, Maryland. Dr. Hill is rated as an Experienced provider by MediFind in the treatment of Turner Syndrome. His top areas of expertise are Infertility, Triploidy, Ovarian Hyperstimulation Syndrome, Endoscopy, and Salpingo-Oophorectomy.

Jaclyn Murry is a Medical Genetics provider in Baltimore, Maryland. Dr. Murry is rated as an Experienced provider by MediFind in the treatment of Turner Syndrome. Her top areas of expertise are Mosaicism, Turner Syndrome, and Intersex.

Ryan Miller is a Pediatric Endocrinologist in Baltimore, Maryland. Dr. Miller is rated as an Experienced provider by MediFind in the treatment of Turner Syndrome. His top areas of expertise are Short Stature (Growth Disorders), Idiopathic Short Stature (ISS), Familial Short Stature (FSS), and Precocious Puberty.