Overview
Michele Spencer-Manzon is a Medical Genetics provider practicing medicine in New Haven, Connecticut.
Dr. Spencer-Manzon is highly rated in 14 conditions, according to our data. Her clinical expertise encompasses Maple Syrup Urine Disease, Tyrosinemia Type 3, Tyrosinemia Type 1, and Tyrosinemia Type 2.
She is actively involved in clinical research, co-authoring 17 peer reviewed articles. Dr. Spencer-Manzon is currently accepting new patients.
Specialties
Licenses
Hospital Affiliations
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- HMO
- PPO
- HMO
- POS
- 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
1 Long Wharf Dr, New Haven, CT 06511
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.
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.
Yale University
Yong-hui Jiang is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New Haven, Connecticut. Dr. Jiang is highly rated in 6 conditions, according to our data. His clinical expertise encompasses Angelman Syndrome, Autism Spectrum Disorder, MELAS Syndrome, and Prader-Willi Syndrome.
Elaine Pereira is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New York, New York. Dr. Pereira is highly rated in 7 conditions, according to our data. Her clinical expertise encompasses Chromosome 6q Deletion, Chromosome 13q Duplication, Trisomy 13, and Micrognathia.
Frequently Asked Questions about Dr. Michele J. Spencer-Manzon
How do I make an appointment with Dr. Michele J. Spencer-Manzon?
You can book an appointment with Dr. Michele J. Spencer-Manzon by calling their office at 203-764-9199. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Michele J. Spencer-Manzon a top-rated expert for Maple Syrup Urine Disease?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Michele J. Spencer-Manzon is classified as an Advanced expert for Maple Syrup Urine Disease, 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. Michele J. Spencer-Manzon specialize in?
While Dr. Michele J. Spencer-Manzon is a Medical Genetics, they have specific expertise in Maple Syrup Urine Disease, Tyrosinemia Type 3, and Tyrosinemia Type 1. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Michele J. Spencer-Manzon participate in research or clinical trials?
Yes. Dr. Michele J. Spencer-Manzon has published 17 articles and abstracts on conditions like Maple Syrup Urine Disease. You can view a list of Dr. Michele J. Spencer-Manzon's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Michele J. Spencer-Manzon accept my insurance?
Dr. Michele J. Spencer-Manzon accepts most major insurance plans, including Aetna and Anthem BCBS. We recommend calling the office directly at 203-764-9199 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
- Advanced
- Beta-Ketothiolase DeficiencyDr. Spencer-Manzon isAdvanced. Learn about Beta-Ketothiolase Deficiency.
- Dihydropteridine Reductase DeficiencyDr. Spencer-Manzon isAdvanced. Learn about Dihydropteridine Reductase Deficiency.
- Fetal Akinesia SequenceDr. Spencer-Manzon isAdvanced. Learn about Fetal Akinesia Sequence.
- Maple Syrup Urine DiseaseDr. Spencer-Manzon isAdvanced. Learn about Maple Syrup Urine Disease.
- Maternal HyperphenylalaninemiaDr. Spencer-Manzon isAdvanced. Learn about Maternal Hyperphenylalaninemia.
- Methylmalonic AcidemiaDr. Spencer-Manzon isAdvanced. Learn about Methylmalonic Acidemia.
- Experienced
- AminoaciduriaDr. Spencer-Manzon isExperienced. Learn about Aminoaciduria.
- Andersen DiseaseDr. Spencer-Manzon isExperienced. Learn about Andersen Disease.
- Arthrogryposis Multiplex CongenitaDr. Spencer-Manzon isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- Congenital ContracturesDr. Spencer-Manzon isExperienced. Learn about Congenital Contractures.
- Cortical DysplasiaDr. Spencer-Manzon isExperienced. Learn about Cortical Dysplasia.
- GABA-Transaminase DeficiencyDr. Spencer-Manzon isExperienced. Learn about GABA-Transaminase Deficiency.
