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Dr. James Ford, MD

Dr. James Ford, MD

Stanford, CA

Accepting patients

Affiliated with a Castle Connolly Top Hospital

    Who is Dr. Ford, Medical Oncologist in Stanford, CA?

    Dr. James Ford, MD is a Medical Oncologist, who primarily practices in Stanford, CA with 1 additional practice location. He is board certified. Dr. Ford completed his residency at Stanford University School of Medicine. Dr. Ford is fluent in English and Spanish, and is currently seeing new patients. Dr. Ford’s practice accepts Kaiser Permanente, Medicaid, Medicare, UnitedHealthcare and other major insurance plans. To book an appointment or to confirm insurance options, please call Dr. Ford’s office at (650) 723-4000.

    What are Areas of Expertise for Dr. Ford?

    Dr. James Ford, MD is a highly-rated, board-certified Medical Oncologist known for expertly diagnosing, treating, and managing a wide array of related conditions and procedures. Utilizing the latest medical advancements and evidence-based practices, Dr. Ford empowers patients to confidently navigate their health journey, specializing in Breast Cancer Genetics, Cancer Genetics, Gastrointestinal Cancer, Hereditary Cancer, Li-Fraumeni Syndrome, and comprehensive wellness support. Serving the Stanford, CA community, Dr. Ford is dedicated to enhancing lives through expert, patient-centered care.

    Where did Dr. Ford go to medical school and complete their residency?

    • Fellowship: Stanford University School of Medicine,Stanford, Ca, United States

    • Residency: Stanford University School of Medicine

    Is Dr. Ford board certified as a Medical Oncologist?

    Yes, Dr. James Ford, MD is board certified by the American Board of Internal Medicine since 2005

    What languages does Dr. Ford speak?

    Dr. Ford and their clinical team can communicate with patients in the following languages:

    • English

    • Spanish

    What conditions does a Medical Oncologist like Dr. Ford typically treat?

    As a Medical Oncologist, Dr. Ford diagnoses, treats, and manages a wide range of conditions. This condition information is derived from anonymized insurance claims and highlights the medical conditions most commonly treated by Dr. Ford. It provides insight into the doctor’s areas of experience and expertise based on real-world patient encounters from the past two years, updated quarterly. Learn more about our claims-based healthcare methodology here.

    Also known as:

    • Genetic Counseling
    • Genetic risk assessment
    • Hereditary counseling
    • DNA counseling

    ICD-10 Codes:

    • Z7183: Encounter for nonprocreative genetic counseling

    Also known as:

    • Prostate Cancer
    • Prostate Cancer Treatment (PDQ®)
    • Prostatic Carcinoma
    • Prostate Gland Cancer
    • Malignant Prostate Tumor

    ICD-10 Codes:

    • C61: Malignant neoplasm of prostate

    Also known as:

    • Pancreatic Cancer
    • Pancreas Cancer
    • Malignant Pancreatic Tumor
    • Pancreatic Carcinoma

    ICD-10 Codes:

    • C259: Malignant neoplasm of pancreas, unspecified

    Also known as:

    • Family History of Digestive Organ Cancer
    • Family History of Breast Cancer
    • Cancer
    • Family History
    • Breast Cancer
    • Genetic risk for gastrointestinal cancer
    • Family history of GI cancer
    • Hereditary digestive cancer
    • Hereditary breast cancer risk
    • Genetic predisposition to breast cancer
    • Breast cancer in the family

    ICD-10 Codes:

    • Z800: Family history of malignant neoplasm of digestive organs
    • Z803: Family history of malignant neoplasm of breast

    Also known as:

    • Myelodysplastic Syndrome
    • Myelodysplastic Syndromes
    • Myelodysplastic Syndromes Treatment (PDQ®)
    • MDS
    • Preleukemia
    • Bone marrow failure disorder

    ICD-10 Codes:

    • D469: Myelodysplastic syndrome, unspecified

    What procedures does a Medical Oncologist like Dr. Ford typically perform?

    As a Medical Oncologist, Dr. Ford performs a variety of medical procedures. This procedure information is derived from anonymized insurance claims and highlights the medical procedures most commonly performed by Dr. Ford. It provides insight into the doctor’s areas of experience and expertise based on real-world patient encounters from the past two years, updated quarterly. Learn more about our claims-based healthcare methodology here.

    Also known as:

    • Blood Transfusion
    • Blood Transfusion and Donation
    • Blood product transfusion
    • Red blood cell transfusion
    • Plasma transfusion

    CPT Codes:

    • 36430: Transfusion, blood or blood components

    Does Dr. Ford accept my insurance?

    Dr. Ford accepts most major insurance plans. Important: Please call our office at (650) 723-4000 before your appointment to verify that your specific plan and network are accepted.

    What insurance plans does Dr. Ford accept in Stanford, CA?

    Dr. Ford in Stanford, CA accepts plans from many carriers. While this list is updated regularly, it is not a guarantee of coverage.

    Top Insurances

    • All Other Third Party

    • Blue Shield of California

    • Cigna Group

    • CVS Health (formerly Aetna)

    • Federal government of the United States

    • Medicaid

    • Medicare

    • State of California

    • UnitedHealth Group

    • Unknown

    View All Insurances

    Where is Dr. Ford's office located?

    Dr. James Ford's Primary Practice

    300 Pasteur Dr

    Stanford, CA 94305

    (650) 723-4000

    Get Directions

    Dr. James Ford's Practice 2

    875 Blake Wilbur Dr

    Palo Alto, CA 94304

    Get Directions

    Recognitions

    Publications

    Molecular Profiling of Gastric Cancer: Toward Persolized Cancer Medicine

    , 2013

    Lupus Antibody Tops Cancer Cells

    , 2012

    Lynch Syndrome in Patients With Colorectal Cancer Finding the Needle in the Haystack

    , 2012

    Long-Term Survivors of Gastric Cancer: A California Population-Based Study

    , 2012

    Genetic Testing by Cancer Site Stomach

    , 2012

    Breast cancers with compromised D repair exhibit selective sensitivity to elesclomol

    , 2012

    Strategies to Identify the Lynch Syndrome Among Patients With Colorectal Cancer A Cost

    , 2011

    Second Primary Breast Cancer Occurrence According to Hormone Receptor Status

    , 2009

    Defective Repair of Oxidative D Damage in Triple

    , 2009

    Performance of BRCA1/2 mutation prediction models in Asian Americans

    , 2008

    CDH1 truncating mutations in the E-cadherin gene

    , 2007

    Predicting and preventing hereditary colorectal cancer

    , 2006

    Molecular inversion probe alysis of gene copy alterations reveals distinct categories of colorectal

    , 2006

    Opposing effects of the UV lesion repair protein XPA

    , 2006

    In vivo recruitment of XPC to UV-induced cyclobutane pyrimidine dimers by the DDB2 gene product

    , 2003

    p53 and regulation of D damage recognition during nucleotide excision repair

    , 2003

    The DDB2 nucleotide excision repair gene product p48 enhances global genomic repair

    , 2003

    p53 and D damage-inducible expression of the xeroderma pigmentosum group C gene

    , 2002

    BRCA1 induces D damage recognition factors and enhances nucleotide excision repair

    , 2002

    Expression of the p48 xeroderma pigmentosum gene is p53-dependent

    , 1999

    Expression of wild-type p53 is required for efficient global genomic nucleotide excision repair in

    , 1997

    LI-FRAUMENI SYNDROME FIBROBLASTS HOMOZYGOUS FOR P53 MUTATIONS ARE DEFICIENT IN GLOBAL D

    , 1995

    Dymic contrast-enhanced MRI

    , 2013

    A young woman with bilateral breast cancer

    , 2013

    Seventh Edition (2010) of the AJCC

    , 2013

    Chest Wall Leiomyosarcoma After Breast-Conservative Therapy for Early

    , 2012

    Single Cell Profiling of Circulating Tumor Cells

    , 2012

    Family History As a Positive Prognostic Factor in Gastric Cancer

    , 2012

    Identification of a Functiol In Vivo p53 Response Element

    , 2012

    A Prospective Study of Total Gastrectomy for CDH1-Positive Hereditary Diffuse Gastric Cancer

    , 2011

    Intensity-Modulated Radiation Therapy Versus Conventiol Radiation Therapy for Squamous Cell

    , 2011

    Comparison of Intensity-Modulated Radiotherapy

    , 2010

    (18)FLUORODEOXYGLUCOSE PET IS PROGNOSTIC OF PROGRESSION

    , 2010

    Oncogenic BRAF Mutation with CDKN2A Ictivation Is Characteristic of a Subset of Pediatric Malignt

    , 2010

    Identification of a biomarker panel using a multiplex proximity ligation

    , 2009

    The role of the retinoblastoma

    , 2009

    Gemcitabine chemotherapy

    , 2008

    Microsatellite instability

    , 2008

    Risk-reducing total gastrectomy for germline mutations in E-cadherin (CDH1)

    , 2008

    Magnetic resonce galactography

    , 2008

    HDAC inhibitor PCI-24781 decreases RAD51 expression and inhibits homologous recombition

    , 2007

    Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer

    , 2007

    Ductal pattern enhancement on magnetic resonce imaging of the breast due to ductal lavage

    , 2007

    A kise-independent function of c

    , 2006

    Colorectal Cancer Screening Clinical Practice Guidelines.

    , 2006

    Phase II study to assess the efficacy of conventiolly fractioted radiotherapy followed by a

    , 2005

    Regulation of D damage recognition and nucleotide excision repair: Another role for p53

    , 2005

    Phase II study of gefitinib, fluorouracil

    , 2005

    Phase I study of stereotactic radiosurgery in patients with locally advanced pancreatic cancer

    , 2004

    Breast magnetic resonce image screening

    , 2004

    Functiol characterization of global genomic D repair and its implications for cancer

    , 2003

    BRCA1 and p53: compensatory roles in D repair

    , 2003

    Defective double-strand D break repair and chromosomal translocations by MYC overexpression

    , 2003

    Phase II trial of preoperative 3D conformal radiotherapy, protracted venous infusion 5-fluorouracil

    , 2003

    D Damage, Repair, and Diseases.

    , 2002

    The p53-regulated cyclin-dependent kise inhibitor

    , 2001

    Protracted venous infusion 5-fluorouracil with concomitant radiotherapy compared with bolus 5

    , 2001

    Preoperative chemoradiation for margilly resectable adenocarcinoma of the pancreas

    , 2001

    Adjuvant chemoradiotherapy for unfavorable carcinoma of the ampulla of vater - Prelimiry report

    , 2001

    Adjuvant radiotherapy

    , 2000

    Decreased UV sensitivity

    , 2000

    p53-mediated D repair responses to UV radiation: Studies of mouse cells lacking p53, p21, and

    , 2000

    Chemoradiotherapy in the magement of localized tumors of the pancreas

    , 1999

    Hepatitis B x protein inhibits p53-dependent D repair in primary mouse hepatocytes

    , 1998

    Role of D excision repair gene defects in the etiology of cancer

    , 1997

    Experimental reversal of P-glycoprotein

    , 1996

    PREFERENTIAL REPAIR OF ULTRAVIOLET LIGHT-INDUCED D

    , 1994

    MODULATION OF RESISTANCE TO ALKYLATING-AGENTS IN CANCER CELL BY GOSSYPOL ENTIOMERS

    , 1991

    BIOCHEMICAL CORRELATES OF THE ANTITUMOR AND ANTIMITOCHONDRIAL PROPERTIES OF GOSSYPOL ENTIOMERS

    , 1990

    TOREMIFENE - PHARMACOLOGIC AND PHARMACOKINETIC BASIS OF REVERSING MULTIDRUG RESISTANCE

    , 1989

    Molecular Profiling of Gastric Cancer: Toward Personalized Cancer Medicine

    , 2013

    Lupus Antibody Tops Cancer Cells

    , 2012

    Lynch Syndrome in Patients With Colorectal Cancer Finding the Needle in the Haystack

    , 2012

    Long-Term Survivors of Gastric Cancer: A California Population-Based Study

    , 2012

    Genetic Testing by Cancer Site Stomach

    , 2012

    Breast cancers with compromised DNA repair exhibit selective sensitivity to elesclomol

    , 2012

    Is breast cancer a part of Lynch syndrome?

    , 2012

    Strategies to Identify the Lynch Syndrome Among Patients With Colorectal Cancer A Cost

    , 2011

    Enhanced sensitivity to cisplatin

    , 2011

    Synergistic Chemosensitivity of Triple-Negative Breast Cancer Cell Lines to Poly

    , 2010

    Second Primary Breast Cancer Occurrence According to Hormone Receptor Status

    , 2009

    Defective Repair of Oxidative DNA Damage in Triple

    , 2009

    Performance of BRCA1/2 mutation prediction models in Asian Americans

    , 2008

    Hereditary diffuse gastric cancer - Implications of genetic testing for screening

    , 2008

    CDH1 truncating mutations in the E-cadherin gene

    , 2007

    Predicting and preventing hereditary colorectal cancer

    , 2006

    Molecular inversion probe analysis of gene copy alterations reveals distinct categories of

    , 2006

    Opposing effects of the UV lesion repair protein XPA

    , 2006

    In vivo recruitment of XPC to UV-induced cyclobutane pyrimidine dimers by the DDB2 gene product

    , 2003

    p53 and regulation of DNA damage recognition during nucleotide excision repair

    , 2003

    The DDB2 nucleotide excision repair gene product p48 enhances global genomic repair

    , 2003

    p53 responsive nucleotide excision repair gene products p48 and XPC, but not p53

    , 2003

    p53 and DNA damage-inducible expression of the xeroderma pigmentosum group C gene

    , 2002

    BRCA1 induces DNA damage recognition factors and enhances nucleotide excision repair

    , 2002

    Xeroderma pigmentosum p48 gene enhances global genomic repair and suppresses UV-induced mutagenesis

    , 2000

    Expression of the p48 xeroderma pigmentosum gene is p53-dependent

    , 1999

    Expression of wild-type p53 is required for efficient global genomic nucleotide excision repair in

    , 1997

    LI-FRAUMENI SYNDROME FIBROBLASTS HOMOZYGOUS FOR P53 MUTATIONS ARE DEFICIENT IN GLOBAL DNA

    , 1995

    A clinical trial of lovastatin for modification of biomarkers associated with breast cancer risk.

    , 2013

    Dynamic contrast-enhanced MRI

    , 2013

    A young woman with bilateral breast cancer

    , 2013

    Seventh Edition (2010) of the AJCC

    , 2013

    Breast cancer risk factors differ between Asian and white women with BRCA1/2 mutations

    , 2012

    Chest Wall Leiomyosarcoma After Breast-Conservative Therapy for Early

    , 2012

    Clinicopathologic and molecular features of sporadic early-onset colorectal adenocarcinoma

    , 2012

    Single Cell Profiling of Circulating Tumor Cells

    , 2012

    Intensity-Modulated Radiotherapy for Pancreatic Adenocarcinoma

    , 2012

    Family History As a Positive Prognostic Factor in Gastric Cancer

    , 2012

    Identification of a Functional In Vivo p53 Response Element

    , 2012

    Identification of a novel deletion mutant strain in Saccharomyces cerevisiae that results in a

    HER2 Expression in Gastric and Gastroesophageal Junction Adenocarcinoma in a US Population

    , 2012

    A Prospective Study of Total Gastrectomy for CDH1-Positive Hereditary Diffuse Gastric Cancer

    , 2011

    Intensity-Modulated Radiation Therapy Versus Conventional Radiation Therapy for Squamous Cell

    , 2011

    A two-antibody mismatch repair protein immunohistochemistry screening approach for colorectal

    , 2011

    Asian ethnicity and breast cancer subtypes: a study from the California Cancer Registry

    , 2011

    Expression of p16(INK4A) But Not Hypoxia Markers or Poly Adenosine Diphosphate

    , 2010

    Poly(ADP-Ribose) Polymerase Inhibition: Targeted Therapy for Triple-Negative Breast Cancer

    , 2010

    PARP inhibitors in breast cancer.

    , 2010

    Comparison of Intensity-Modulated Radiotherapy

    , 2010

    (18)FLUORODEOXYGLUCOSE PET IS PROGNOSTIC OF PROGRESSION

    , 2010

    Hereditary diffuse gastric cancer due to a previously undescribed CDH1 splice site mutation

    , 2010

    Pathological response after chemoradiation for T3 rectal cancer

    , 2010

    Pathological response after chemoradiation for T3 rectal cancer.

    , 2010

    Novel Treatment Approaches for Triple-Negative Breast Cancer

    , 2010

    Longer Relative Telomere Length in Blood from Women with Sporadic

    , 2010

    Oncogenic BRAF Mutation with CDKN2A Inactivation Is Characteristic of a Subset of Pediatric

    , 2010

    PARP Inhibitors for the Treatment and Prevention of Breast Cancer.

    , 2010

    Multimodality treatment with intensity modulated radiation therapy for esophageal cancer

    , 2010

    Identification of a biomarker panel using a multiplex proximity ligation

    , 2009

    A BRCA2 founder mutation

    , 2009

    The role of the retinoblastoma

    , 2009

    Detection of Solitary Humeral Metastasis From Pancreatic Adenocarcinoma With F-18 FDG PET/CT

    , 2009

    Stereotactic Radiotherapy for Unresectable Adenocarcinoma of the Pancreas

    , 2009

    Gemcitabine chemotherapy

    , 2008

    Microsatellite instability

    , 2008

    Cancer risk reduction and reproductive concerns in female BRCA1/2 mutation carriers

    , 2008

    Risk-reducing total gastrectomy for germline mutations in E-cadherin (CDH1)

    , 2008

    Characterization of the pathogenic mechanism of a novel BRCA2 variant in a Chinese family

    , 2008

    Identification of a novel p53 in-frame deletion in a Li-Fraumeni-like family

    , 2008

    Magnetic resonance galactography

    , 2008

    HDAC inhibitor PCI-24781 decreases RAD51 expression and inhibits homologous recombination

    , 2007

    A carrier of both MEN1 and BRCA2 mutations: case report a-lid review of the literature

    , 2007

    Identification of an intronic single nucleotide polymorphism leading to allele dropout during

    , 2007

    Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer

    , 2007

    Ductal pattern enhancement on magnetic resonance imaging of the breast due to ductal lavage

    , 2007

    Reversal of stathmin-mediated resistance to paclitaxel

    , 2007

    Germ line mutations of mismatch repair genes

    , 2006

    A kinase-independent function of c

    , 2006

    Colorectal Cancer Screening Clinical Practice Guidelines.

    , 2006

    Genetic/familial high-risk assessment: breast and ovarian.

    Phase II study to assess the efficacy of conventionally fractionated radiotherapy followed by a

    , 2005

    Regulation of DNA damage recognition and nucleotide excision repair: Another role for p53

    , 2005

    Opinions of women with high inherited breast cancer risk about prophylactic mastectomy

    , 2005

    Phase II study of gefitinib, fluorouracil

    , 2005

    Characterization of a recurrent germ line mutation of the E-cadherin gene

    , 2005

    Ductal lavage of fluid-yielding and non

    , 2005

    Phase I study of stereotactic radiosurgery in patients with locally advanced pancreatic cancer

    , 2004

    Breast magnetic resonance image screening

    , 2004

    Functional characterization of global genomic DNA repair and its implications for cancer

    , 2003

    BRCA1 and p53: compensatory roles in DNA repair

    , 2003

    Defective double-strand DNA break repair and chromosomal translocations by MYC overexpression

    , 2003

    Phase II trial of preoperative 3D conformal radiotherapy, protracted venous infusion 5-fluorouracil

    , 2003

    DNA Damage, Repair, and Diseases.

    , 2002

    The p53-regulated cyclin-dependent kinase inhibitor

    , 2001

    Protracted venous infusion 5-fluorouracil with concomitant radiotherapy compared with bolus 5

    , 2001

    Radiotherapy, concomitant protracted-venous-infusion 5-fluorouracil

    , 2001

    Preoperative chemoradiation for marginally resectable adenocarcinoma of the pancreas

    , 2001

    Adjuvant chemoradiotherapy for unfavorable carcinoma of the ampulla of vater - Preliminary report

    , 2001

    Adjuvant radiotherapy

    , 2000

    Proapoptotic p53-interacting protein 53BP2 is induced by UV irradiation but suppressed by p53

    , 2000

    Reduced global genomic repair of ultraviolet light

    , 2000

    Decreased UV sensitivity

    , 2000

    p53-mediated DNA repair responses to UV radiation: Studies of mouse cells lacking p53, p21, and

    , 2000

    Chemoradiotherapy in the management of localized tumors of the pancreas

    , 1999

    Hepatitis B x protein inhibits p53-dependent DNA repair in primary mouse hepatocytes

    , 1998

    Human fibroblasts expressing the human papillomavirus E6 gene are deficient

    , 1998

    Role of DNA excision repair gene defects in the etiology of cancer

    , 1997

    Experimental reversal of P-glycoprotein

    , 1996

    P-glycoprotein-mediated multidrug resistance

    , 1996

    MODULATORS OF MULTIDRUG-RESISTANCE - PRECLINICAL STUDIES

    , 1995

    PREFERENTIAL REPAIR OF ULTRAVIOLET LIGHT-INDUCED DNA

    , 1994

    PHARMACOLOGICAL CIRCUMVENTION OF MULTIDRUG-RESISTANCE

    , 1993

    EFFECT OF BUTHIONINE SULFOXIMINE ON TOXICITY OF VERAPAMIL AND DOXORUBICIN TO MULTIDRUG RESISTANT

    , 1991

    MODULATION OF RESISTANCE TO ALKYLATING-AGENTS IN CANCER CELL BY GOSSYPOL ENANTIOMERS

    , 1991

    PHARMACOLOGY OF DRUGS THAT ALTER MULTIDRUG RESISTANCE IN CANCER

    , 1990

    BIOCHEMICAL CORRELATES OF THE ANTITUMOR AND ANTIMITOCHONDRIAL PROPERTIES OF GOSSYPOL ENANTIOMERS

    , 1990

    CELLULAR AND BIOCHEMICAL

    , 1990

    TOREMIFENE - PHARMACOLOGIC AND PHARMACOKINETIC BASIS OF REVERSING MULTIDRUG RESISTANCE

    , 1989

    STRUCTURAL FEATURES DETERMINING ACTIVITY OF PHENOTHIAZINES AND RELATED DRUGS FOR INHIBITION OF CELL

    , 1989

    What is Dr. Ford's NPI number?An National Provider Identifier (NPI) is a unique ID number that identifies doctors and healthcare providers nationwide.

    Dr. Ford's National Provider Identifier (NPI) number is 1801922604.

    What common questions do patients ask about Dr. Ford?

    Here are answers to patients Frequently Asked Questions (FAQ’s) about Dr. Ford

    What is Dr. James Ford's specialty?

    Dr. Ford is a Medical Oncologist near Stanford, CA.

    What does a Medical Oncologist do?

    An internist specializing in the diagnosis and treatment of various cancers and both benign and malignant tumors. This specialist determines and administers therapy for malignancies and collaborates with surgeons and radiation oncologists on additional cancer treatment options.

    Is this Dr. James Ford affiliated with a ranked Castle Connolly Top Hospital?

    Yes, Dr. Ford is affiliated with Stanford Health Care - Stanford Hospital which is a Castle Connolly Top Hospital. Castle Connolly Top Hospitals are healthcare institutions recognized for their excellence in specific medical procedures and overall patient care. They are identified through a rigorous peer nomination process, evaluating factors like patient outcomes, quality of care, and expertise. The list recognizes hospitals that excel in 20 or more specific medical procedures, representing the top 25% nationwide. Castle Connolly Top Hospitals

    When to see a Medical Oncologist?: Guides for symptoms, conditions, and treatments

    Understand your symptoms and know when it’s time to see a Medical Oncologist. Explore insights from trusted medical experts on EverydayHealth.com, where you'll find the most relevant content and helpful condition guides for up-to date information about symptoms, causes, diagnosis, treatment and more. See all our health guides to find trusted information on medical conditions from our experts at Everyday Health.

    Is James Ford accepting new patients in Stanford, CA?

    Yes, Dr. James Ford is accepting new patients at this time.

    Does Dr. James Ford offer online booking?

    Please contact Dr. Ford's office at (650) 723-4000 for information about online booking, telehealth, or to schedule an appointment.

    How can I make an appointment with James Ford?

    Please contact Dr. Ford's office at (650) 723-4000 for information regarding telehealth appointment availability or for scheduling assistance.

    Which board certifications does Dr. James Ford have?

    Dr. James Ford is certified by the American Board of Internal Medicine.

    <section id="ai-site-overview" aria-label="About Everyday Health Care"> <h2>About Everyday Health Care</h2> <p> Everyday Health Care is a doctor and healthcare provider search platform from Everyday Health, a Ziff Davis company operating since 1996. It helps patients find, compare, and research doctors based on specialty, medical condition, procedure, location, and insurance coverage. </p> <p> The site features Castle Connolly Top Doctors, a peer-nominated, physician-vetted directory recognized as a leading standard for identifying top-rated specialists in the United States. Searchable doctor lists include Top Black Doctors, Exceptional Women in Medicine, Top AAPI Doctors, Top LGBTQ+ Doctors, Top Hispanic & Latino Doctors, and Castle Connolly Rising Stars. </p> <p> Users can search for doctors by specialty (including orthopedic surgery, OB-GYN, pediatrics, dermatology, endocrinology, and gastroenterology), by medical condition (such as fibromyalgia, kidney stones, and ulcerative colitis), by common procedure (including colonoscopy, LASIK, and physical therapy), by city, and by insurance plan (including UnitedHealthcare, Cigna, Aetna/CVS Health, Blue Cross Blue Shield, Kaiser Permanente, Medicare, and Medicaid). </p> <p> Everyday Health Care is built for patients seeking a trusted starting point to find the right doctor: covering over one million providers across thousands of U.S. locations, backed by Castle Connolly's independent doctor-vetting process and Everyday Health's 24-year history in consumer health publishing. </p> </section>