Peter J. Hulick, M.D.

Peter J. Hulick, M.D.

Peter J. Hulick, M.D.

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Conditions & Procedures

Conditions

Albinism, Alkaptonuria, Alpha-1-Antitrypsin, Alport Syndrome, Alzheimer's Disease, Amyotrophic Lateral Sclerosis (ALS), Ataxia , Ataxia Telangiectasia, Autism, Bannayan-Riley-Ruvalcaba syndrome, Bardet Biedl Syndrome, Batten Disease, Birt-Hogg-Dube, Brain Cancer, Brugada Syndrome, Camurati-Engelmann Disease, Carcinoid, Cardiomyopathy, Carney Complex, Celiac Disease, Centronuclear Myotubular Myopathy, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL), Cerebral Cavernous Malformations (CCMs), Cervical Cancer, Charcot-Marie-Tooth, Chromosomal Disorders, Colon Cancer, Cone Rod Dystrophy (CRD), Congenital Adrenal Hyperplasia (CAH), Congenital Heart Disease, Cystic Fibrosis, Dermatomyositis, Dystonia, Ehlers-Danlos, Fabry Disease, Familial Adenomatous Polyposis (FAP)/MAP, Familial Amyloidosis, Familial Aneurysm, Familial Aortic Aneurysms, Familial Cold Autoinflammatory Syndrome (FCAS), Familial Dysautonomia (FD), Familial Hypocalciuric Hypercalcemia (FHH), Familial Mediterranean Fever (FMF), Fragile X syndrome (FXS), Galactosemia, Gallbladder Cancer, Gastrointestinal Stromal Tumor (GIST), Gaucher Disease, General Genetic Syndromes, Gilbert Syndrome, Gitelman Syndrome, Glomerulopathy, Head and Neck Cancer, Hearing Loss, Hemagophagocytic Syndrome, Hemochromotosis, Hemophilia, Hereditary Dementias, Hereditary Diffuse Gastric Cancer, Hereditary Hemorrahgic Telangiestasia (HHT), Hereditary Leiomyomatosis with Renal Cell Cancer (HLRCC), Hereditary Neuropathy with Liability to Pressure Palsies (HNPP), Huntington's Disease, Huntington's Disease (HD), Hyperparathyroidism, Hypochondroplasia, Hypophosphatemic Rickets, Infertility, Juvenile Polyposis Syndrome, Kennedy's Disease, Kidney Cancer, Long QT, Long QT syndrome (LQTS), Lynch Syndrome, Malignant Hyperthermia (MH), Marfan Syndrome, Melanoma, Mental Retardation (MR), Metabolic Disorders, Mitochondrial Disorders, Multiple Congenital Anomalies (MCA), Multiple Endocrine Neoplasia Type 1 (MEN1), Multiple Endocrine Neoplasia Type 2 (MEN2), Multiple Endocrine Neoplasia Type 2B (MEN2B), Muscular Dystrophies (MD), Myotonic Dystrophy, Neurofibromatosis (NF), Neurological Disease, Noonan Syndrome (NS), Norrie Disease, Ollier Disease, Ornithine Transcarbamylase (OTC), Osteogenesis Imperfecta (OI), Ovarian Cancer, Pancreatic Cancer, Pancreatitis, Paraganglioma, Parkinson's Disease (PD), Pediatric Genetic Disorders, Peutz-Jeghers Syndrome, Pheochromocytoma, Polycystic Kidney Disease (PKD), Prader-Willi Syndrome (PWS), Rectal Cancer, Russell-Silver Syndrome (RSS), Sarcoma, Schizencephaly, Schwannoma, Sebaceous Carcinoma, Small Bowel Cancer, Spinal Muscular Atrophy (SMA), Spinocerebellar Ataxia (SCA), Stargardt's Disease, Stickler Syndrome, Stomach Cancer, Thrombophilia, Thyroid Cancer, Treacher Collins syndrome (TCS), Tuberous Sclerosis (TSC), Uterine Cancer, Von Hippel Lindau, Williams syndrome (WS)

Procedures

Breast Cancer (BRCA) Gene Test, Genomic Screening, Pharmacogenetic Testing

General Information

Gender

Male

Affiliation

NorthShore Medical Group

Academic Rank

Clinical Assistant Professor

Languages

English

Board Certified

Clinical Genetics (M.D.), Internal Medicine

Education, Training & Fellowships

Medical School

Jefferson Medical College, 2001

Residency

Mayo Clinic/St. Luke's Hospital, 2002
Children's Hospital Boston/Beth Israel Harvard University, 2007

Locations

A

NorthShore Medical Group

1000 Central St.
Suite 620
Evanston, IL 60201
847.570.1029 847.733.5318 fax Get Directions This location is wheelchair accessible.
B

NorthShore Medical Group

757 Park Ave. West
Kellogg Cancer Center
Highland Park, IL 60035
847.570.1029 847.733.5318 fax Get Directions This location is wheelchair accessible.

Insurance

In the News

Jul 2015

May 2015

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Featured Videos

Don Burzen and his physicians discuss the discovery of his genetic mutation by the Northshore Center for Personalized Medicine.

Don Burzen and his physicians discuss the discovery of his genetic mutation by the Northshore Center for Personalized Medicine.

Sivan Schondorf talks about how genetic counseling helped with her decision to undergo genetic testing for the BRCA1/BRCA2 gene mutation.

Sivan Schondorf talks about how genetic counseling helped with her decision to undergo genetic testing for the BRCA1/BRCA2 gene mutation.

Learn more about the NorthShore Center for Personalized Medicine.

Learn more about the NorthShore Center for Personalized Medicine.

Dr. Hulick discusses how to prepare for a cancer genetics evaluation.

Dr. Hulick discusses how to prepare for a cancer genetics evaluation.

Dr. Hulick discusses the role genetics has in a kidney cancer diagnosis.

Dr. Hulick discusses the role genetics has in a kidney cancer diagnosis.