Overview
Maria Schwab is a Medical Genetics provider practicing medicine in Newark, New Jersey.
Her clinical expertise encompasses Autism Spectrum Disorder, Chromosome 13q Deletion, Chromosome 2 Uniparental Disomy, and Mosaic Variegated Aneuploidy Syndrome.
She is actively involved in clinical research, co-authoring 2 peer reviewed articles.
Specialties
Licenses
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- POS
- HMO
- INDEMNITY
- POS
- PPO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE PART D
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
183 S Orange Ave # F, Newark, NJ 07103
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.
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Cohen Children's Northwell Health Physician Partners Medical Genetics
Dr. Ian Daniel Krantz, MD, is a renowned physician specializing in Genetics and Pediatrics. He currently sees patients at Cohen Children's Medical Center (CCMC) and Northwell Health Physician Partners Medical Genetics. Dr. Krantz holds certifications in Clinical Genetics, Cytogenetics, and Pediatrics from the American Board of Medical Genetics and the American Board of Pediatrics, respectively.Dr. Krantz completed his BFA at Concordia University in Montreal and his MD at Sackler School of Medicine (Tel Aviv University). He completed his residency in Medical Genetics at Children's Hospital of Philadelphia and his residency in Pediatrics at New York University Medical Center.With an impressive set of academic and administrative titles, Dr. Krantz serves as the Division Chief of Pediatric Genetics and Genomics at Cohen Children's Medical Center and is the System Vice President for Pediatric Genetics at Northwell Health. Additionally, he holds the position of Professor at the Zucker School of Medicine at Northwell Health.Dr. Krantz is recognized for his clinical expertise in isolated and syndromic forms of congenital birth differences and developmental diagnoses, including syndromic and non-syndromic autism. He has a special interest in the genetics of hearing loss and focused expertise in Cornelia de Lange Syndrome, Pallister-Killian syndrome, Alagille syndrome, CHOPS syndrome, among others.Dr. Krantz's research is dedicated to identifying and characterizing the molecular etiology of syndromic and non-syndromic developmental diagnoses. His research lab has made significant contributions in the field, discovering new disease genes and shedding light on critical molecular pathways involved in human developmental disorders.Driven by his commitment to advancing patient care, Dr. Krantz has been at the forefront of integrating genomic technologies into the clinical setting. He has implemented rapid genome sequencing into the NICU and CICU and established biobanks and biorepositories to further research efforts. Through his work, he aims to understand the impact of complex diagnostic information on clinicians and families involved.With his extensive expertise and dedication to advancing genetic research and patient care, Dr. Krantz continues to make significant contributions to the field of Pediatrics and Genetics. Dr. Krantz is highly rated in 15 conditions, according to our data. His clinical expertise encompasses Cornelia De Lange Syndrome, Pallister-Killian Mosaic Syndrome, Mosaicism, and KBG Syndrome.
Robert Desnick is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New York, New York. Dr. Desnick is highly rated in 8 conditions, according to our data. His clinical expertise encompasses Hereditary Coproporphyria, Fabry Disease, Aplasia Cutis Congenita, and Ectodermal Dysplasias.
Frequently Asked Questions about Dr. Maria Schwab
How do I make an appointment with Dr. Maria Schwab?
You can book an appointment with Dr. Maria Schwab by calling their office at 973-972-3818. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Maria Schwab a top-rated expert for Autism Spectrum Disorder?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Maria Schwab is classified as an Experienced expert for Autism Spectrum Disorder, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
What conditions does Dr. Maria Schwab specialize in?
While Dr. Maria Schwab is a Medical Genetics, they have specific expertise in Autism Spectrum Disorder, Chromosome 13q Deletion, and Chromosome 2 Uniparental Disomy. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Maria Schwab participate in research or clinical trials?
Yes. Dr. Maria Schwab has published 2 articles and abstracts on conditions like Autism Spectrum Disorder. You can view a list of Dr. Maria Schwab's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Maria Schwab accept my insurance?
Dr. Maria Schwab accepts most major insurance plans, including Horizon Healthcare and Humana. We recommend calling the office directly at 973-972-3818 to verify that your specific plan is currently accepted before your visit.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as 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.
Learn more about MediFind’s expert tiers
- Experienced
- Autism Spectrum DisorderDr. Schwab isExperienced. Learn about Autism Spectrum Disorder.
- Chromosome 11 Uniparental DisomyDr. Schwab isExperienced. Learn about Chromosome 11 Uniparental Disomy.
- Chromosome 13q DeletionDr. Schwab isExperienced. Learn about Chromosome 13q Deletion.
- Chromosome 2 Uniparental DisomyDr. Schwab isExperienced. Learn about Chromosome 2 Uniparental Disomy.
- Chromosome 6 Uniparental DisomyDr. Schwab isExperienced. Learn about Chromosome 6 Uniparental Disomy.
- Mosaic Variegated Aneuploidy SyndromeDr. Schwab isExperienced. Learn about Mosaic Variegated Aneuploidy Syndrome.
