Overview
Rebecca Ahrens-Nicklas is a Pediatrics specialist and a Medical Genetics provider in Philadelphia, Pennsylvania. Dr. Ahrens-Nicklas has been practicing medicine for over 14 years is highly rated in 12 conditions, according to our data. Her top areas of expertise are Multiple Sulfatase Deficiency, Chondrodysplasia Punctata with Steroid Sulfatase Deficiency, Inborn Amino Acid Metabolism Disorder, and Phenylketonuria (PKU).
Her clinical research consists of co-authoring 72 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
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Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Elaine Zackai is a Medical Genetics specialist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Zackai is highly rated in 57 conditions, according to our data. Her top areas of expertise are Micrognathia, DiGeorge Syndrome, Hardikar Syndrome, Sotos Syndrome, and Myringotomy.
Michael Bober is a Medical Genetics specialist and a Pediatrics provider in Wilmington, Delaware. Dr. Bober is highly rated in 35 conditions, according to our data. His top areas of expertise are Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2), Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1), Achondroplasia, Osteotomy, and Myringotomy. Dr. Bober is currently accepting new patients.
Jennifer Kalish is a Medical Genetics provider in Philadelphia, Pennsylvania. Dr. Kalish is highly rated in 19 conditions, according to our data. Her top areas of expertise are Beckwith-Wiedemann Syndrome, Macroglossia, Hemi 3 Syndrome, Hemihyperplasia, and Glossectomy.
Areas of Expertise
When evaluating expertise, MediFind pulls from factors such as the number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
To learn more about how MediFind determines the expertise levels, check out our expert tiers page.
- Distinguished
- Chondrodysplasia Punctata with Steroid Sulfatase Deficiency
- Inborn Amino Acid Metabolism Disorder
- Phenylketonuria (PKU)
- Advanced
- Cardiomyopathic Lentiginosis
- Coffin-Siris Syndrome
- Leukodystrophy
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Micrognathia
- Noonan Syndrome