Overview
Joshua Baker is a Pediatrics provider practicing medicine in Chicago, Illinois.
Dr. Baker is highly rated in 43 conditions, according to our data. His clinical expertise encompasses Urea Cycle Disorders (UCD), Acid Sphingomyelinase Deficiency (ASMD), Niemann-Pick Disease, and Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome).
He is actively involved in clinical research, co-authoring 23 peer reviewed articles.
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
- 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 MANAGED MEDICAID
- OTHER MEDICAID
- STATE MEDICAID
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- HMO
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- OTHER COMMERCIAL
- OTHER MEDICARE PART D
- OTHER COMMERCIAL
- 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
225 E Chicago Ave, Chicago, IL 60611
300 Longwood Ave, Boston, MA 02115
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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Lurie Children's Medical Group Inc.
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Frequently Asked Questions about Dr. Joshua J. Baker
How do I make an appointment with Dr. Joshua J. Baker?
You can book an appointment with Dr. Joshua J. Baker by calling their office at 312-227-4000. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Joshua J. Baker a top-rated expert for Urea Cycle Disorders (UCD)?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Joshua J. Baker is classified as an Distinguished expert for Urea Cycle Disorders (UCD), 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. Joshua J. Baker specialize in?
While Dr. Joshua J. Baker is a Pediatrics, they have specific expertise in Urea Cycle Disorders (UCD), Acid Sphingomyelinase Deficiency (ASMD), and Niemann-Pick Disease. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Pediatrics.
Does Dr. Joshua J. Baker participate in research or clinical trials?
Yes. Dr. Joshua J. Baker has published 23 articles and abstracts on conditions like Urea Cycle Disorders (UCD). You can view a list of Dr. Joshua J. Baker's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Joshua J. Baker accept my insurance?
Dr. Joshua J. Baker accepts most major insurance plans, including Aetna and Cigna. We recommend calling the office directly at 312-227-4000 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
- Distinguished
- Acid Sphingomyelinase Deficiency (ASMD)Dr. Baker isDistinguished. Learn about Acid Sphingomyelinase Deficiency (ASMD).
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Niemann-Pick DiseaseDr. Baker isDistinguished. Learn about Niemann-Pick Disease.
- Urea Cycle Disorders (UCD)Dr. Baker isDistinguished. Learn about Urea Cycle Disorders (UCD).
- Advanced
- Autosomal Recessive Congenital Methemoglobinemia
- Beta-Ketothiolase DeficiencyDr. Baker isAdvanced. Learn about Beta-Ketothiolase Deficiency.
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency
- CHARGE SyndromeDr. Baker isAdvanced. Learn about CHARGE Syndrome.
- Dihydrolipoamide Dehydrogenase Deficiency
- Early Infantile Epileptic Encephalopathy
- Fabry DiseaseDr. Baker isAdvanced. Learn about Fabry Disease.
- GABA-Transaminase DeficiencyDr. Baker isAdvanced. Learn about GABA-Transaminase Deficiency.
- Glutaric Acidemia Type 2Dr. Baker isAdvanced. Learn about Glutaric Acidemia Type 2.
- Glycogen Storage Disease Type 0Dr. Baker isAdvanced. Learn about Glycogen Storage Disease Type 0.
- Glycogen Storage Disease Type 13
- Glycogen Storage Disease Type 3Dr. Baker isAdvanced. Learn about Glycogen Storage Disease Type 3.
- Glycogen Storage Disease Type 7Dr. Baker isAdvanced. Learn about Glycogen Storage Disease Type 7.
- Glycogen Storage Disease Type 9Dr. Baker isAdvanced. Learn about Glycogen Storage Disease Type 9.
- GM1 GangliosidosisDr. Baker isAdvanced. Learn about GM1 Gangliosidosis.
- HyperlysinemiaDr. Baker isAdvanced. Learn about Hyperlysinemia.
- Isovaleric AcidemiaDr. Baker isAdvanced. Learn about Isovaleric Acidemia.
- Koolen De Vries SyndromeDr. Baker isAdvanced. Learn about Koolen De Vries Syndrome.
- Malonyl-CoA Decarboxylase Deficiency
- Microcephaly Deafness SyndromeDr. Baker isAdvanced. Learn about Microcephaly Deafness Syndrome.
- Mucopolysaccharidoses (MPS)Dr. Baker isAdvanced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome)
- PEPCK 1 DeficiencyDr. Baker isAdvanced. Learn about PEPCK 1 Deficiency.
- Phosphoglycerate Kinase Deficiency
- Phosphoglycerate Mutase Deficiency
- Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy
- Pompe DiseaseDr. Baker isAdvanced. Learn about Pompe Disease.
- Pyruvate Carboxylase DeficiencyDr. Baker isAdvanced. Learn about Pyruvate Carboxylase Deficiency.
- Sandhoff DiseaseDr. Baker isAdvanced. Learn about Sandhoff Disease.
- Succinic Semialdehyde Dehydrogenase Deficiency
- Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Von Gierke DiseaseDr. Baker isAdvanced. Learn about Von Gierke Disease.
- Wildervanck SyndromeDr. Baker isAdvanced. Learn about Wildervanck Syndrome.
- Williams SyndromeDr. Baker isAdvanced. Learn about Williams Syndrome.
- X-Linked Creatine DeficiencyDr. Baker isAdvanced. Learn about X-Linked Creatine Deficiency.
- Experienced
- Activated PI3K Delta Syndrome (APDS)Dr. Baker isExperienced. Learn about Activated PI3K Delta Syndrome (APDS).
- AminoaciduriaDr. Baker isExperienced. Learn about Aminoaciduria.
- Autism Spectrum DisorderDr. Baker isExperienced. Learn about Autism Spectrum Disorder.
- Cantu SyndromeDr. Baker isExperienced. Learn about Cantu Syndrome.
- Cardiofaciocutaneous SyndromeDr. Baker isExperienced. Learn about Cardiofaciocutaneous Syndrome.
- ChondrodystrophyDr. Baker isExperienced. Learn about Chondrodystrophy.
- Delayed GrowthDr. Baker isExperienced. Learn about Delayed Growth.
- Fetal Alcohol Syndrome (FAS)Dr. Baker isExperienced. Learn about Fetal Alcohol Syndrome (FAS).
- Gaucher DiseaseDr. Baker isExperienced. Learn about Gaucher Disease.
- Hemi 3 SyndromeDr. Baker isExperienced. Learn about Hemi 3 Syndrome.
- Hereditary AtaxiaDr. Baker isExperienced. Learn about Hereditary Ataxia.
- Hereditary Spastic ParaparesisDr. Baker isExperienced. Learn about Hereditary Spastic Paraparesis.
- Increased Head CircumferenceDr. Baker isExperienced. Learn about Increased Head Circumference.
- Infantile NeutropeniaDr. Baker isExperienced. Learn about Infantile Neutropenia.
- Leigh SyndromeDr. Baker isExperienced. Learn about Leigh Syndrome.
- Liver FailureDr. Baker isExperienced. Learn about Liver Failure.
- Marshall-Smith SyndromeDr. Baker isExperienced. Learn about Marshall-Smith Syndrome.
- Maternally Inherited Leigh SyndromeDr. Baker isExperienced. Learn about Maternally Inherited Leigh Syndrome.
- Megalencephaly-Capillary Malformation Syndrome
- MicrocephalyDr. Baker isExperienced. Learn about Microcephaly.
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A)
- Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B)
- Multiple Epiphyseal DysplasiaDr. Baker isExperienced. Learn about Multiple Epiphyseal Dysplasia.
- Newborn Low Blood SugarDr. Baker isExperienced. Learn about Newborn Low Blood Sugar.
- OmphaloceleDr. Baker isExperienced. Learn about Omphalocele.
- Perlman SyndromeDr. Baker isExperienced. Learn about Perlman Syndrome.
- Phenylketonuria (PKU)Dr. Baker isExperienced. Learn about Phenylketonuria (PKU).
- PIK3CA-Related Overgrowth SpectrumDr. Baker isExperienced. Learn about PIK3CA-Related Overgrowth Spectrum.
- RASopathiesDr. Baker isExperienced. Learn about RASopathies.
- Simpson-Golabi-Behmel SyndromeDr. Baker isExperienced. Learn about Simpson-Golabi-Behmel Syndrome.