Faculty

Institution

Unit

Venue

Kimberly Kripps, M.D.

Assistant Professor of Molecular and Medical Genetics

Oregon Health & Science University

Affiliations

Division Of Genetics

Kimberly Kripps, M.d. is currently serving as a Division Of Genetics Assistant Professor of Molecular and Medical Genetics at Oregon Health & Science University.

Honors

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Experiences

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Education

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Kimberly Kripps, M.D.

Oregon Health & Science University

Assistant Professor of Molecular and Medical Genetics

You can click a keyword to filter the displayed items

genetics genetic disorders human genetics medicine health sciences medical genetics disease gene identification mendelian disorder molecular biology hepatology gene expression molecular neurodegeneration hematology veterinary medicine transcriptome metabolism nutrition clinical lipidology molecular diagnostics metabolic syndrome child nutrition pediatric diabetes clinical nutrition molecular psychiatry genome biology redox biology molecular metabolism molecular physiology ocular surface avian biology clinical investigation child neurology clinical presentation disease mechanisms metabolic disorders disease progression genomic mechanisms mitochondrial function mitochondrial biogenesis genome instability ocular pathology ocular disease clinical case report adrenal disease case studies vascular trauma electronic publishing neonatology genetic testing developmental anomalies paediatric medicine methionine synthase deficiency variable clinical presentation microdeletion spectrum severe phenotype orbital involvement extensive eyelid granulomatous inflammation unusual neuroimaging novel suclg1 variants

Notable Scholarly Works

Notable Federal Grants

Collaborators

Letter to the Editor: Newborn Screening for Low Blood Citrulline Leads to Diagnosis of Ornithine Aminotransferase Deficiency. Molecular Genetics and Metabolism (2026)

pediatricsgenetic disordersmendelian disordermedicinepregnancy hypertensionhuman geneticshealth sciencesgenetic testing

Novel Suclg1 Variants in a Patient With Fatal Neonatal Onset Succinyl-Coa Ligase Deficiency. Journal of Pediatric Genetics (2025)

pathologygenetic disordersmolecular medicinedevelopmental anomaliesnovel suclg1 variants

Feasibility of Newborn Screening for Pyridoxine-Dependent Epilepsy. Molecular Genetics and Metabolism (2024)

pediatricsgenetic disordersmolecular psychiatryepilepsy

P.48 Severe Variant for Pyridoxine Dependent Epilepsy Found in the Micronesian Population: A Case Study. Molecular Genetics and Metabolism (2024)

genetic disordersmolecular neurodegenerationmendelian disorderdisease gene identificationepilepsyhuman geneticsgenetics

Pyridoxine Dependent Epilepsy: Identification of a Founder Variant in the Micronesian Population With Severe Features. Molecular Genetics and Metabolism (2023)

genetic disordersmendelian disorderdisease gene identificationepilepsyheredityhuman geneticsmedical geneticsgenetics

Rubella Virus‐Associated Necrotizing Granulomatous Inflammation With Extensive Eyelid, Ocular, and Orbital Involvement. Pediatric Dermatology (2023)

orbital involvementinfectious diseasesvirologyextensive eyelidpathogenesisocular surfacegranulomatous inflammationocular diseaseocular pathologyinfectious diseases (medical specialty)pathogensophthalmology

ANABOLISM: Practical Strategies. (2022)

surgeryvascular traumavascular surgeryneuromuscular medicine

Loss of Focad, Operating via the Ski Messenger Rna Surveillance Pathway, Causes a Pediatric Syndrome With Liver Cirrhosis. Nature Genetics (2022)

disease mechanismshepatologymolecular diagnosticsmolecular biologygene expressiontranscriptomegenetics

A Novel Intronic Pathogenic Variant in Star With a Dominant Negative Mechanism Causes Attenuated Lipoid Congenital Adrenal Hyperplasia. Journal of Investigative Medicine High Impact Case Reports (2021)

Erin FinnKimberly KrippsChristina ChambersMichele RappNaomi J. L. MeeksFang XuWuyan ChenAustin A. LarsonNatalie J. Nokoff

pathologyadrenal diseasepathogenesisclinical investigationavian biologyclinical case reportmedicineclinical researchcase studiesgenetics

Methionine Synthase Deficiency: Variable Clinical Presentation and Benefit of Early Diagnosis and Treatment. Journal of Inherited Metabolic Disease (2021)

Kimberly A. KrippsLeighann SrembaAustin A. LarsonJohan L.K. Van HoveHoanh NguyenErica L. WrightDavid M. MirskyDavid WatkinsDavid S. RosenblattDavid KetteridgeSusan A. BerryShawn E. McCandlessPeter R. Baker

clinical lipidologyclinical presentationvariable clinical presentationhepatologyhematologypharmacologymedicinemethionine synthase deficiencyveterinary medicinemedical geneticshealth sciences

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Kimberly Kripps, M.D.

Assistant Professor of Molecular and Medical Genetics

Oregon Health & Science University

Affiliations

Division Of Genetics

Kimberly Kripps, M.d. is currently serving as a Division Of Genetics Assistant Professor of Molecular and Medical Genetics at Oregon Health & Science University.

Honors

Create free account to unlock more features

Experiences

Create free account to unlock more features

Education

Create free account to unlock more features

Kimberly Kripps, M.D.

Oregon Health & Science University

Assistant Professor of Molecular and Medical Genetics

You can click a keyword to filter the displayed items

Notable Scholarly Works

Notable Federal Grants

Collaborators

Letter to the Editor: Newborn Screening for Low Blood Citrulline Leads to Diagnosis of Ornithine Aminotransferase Deficiency. Molecular Genetics and Metabolism (2026)

pediatricsgenetic disordersmendelian disordermedicinepregnancy hypertensionhuman geneticshealth sciencesgenetic testing

Novel Suclg1 Variants in a Patient With Fatal Neonatal Onset Succinyl-Coa Ligase Deficiency. Journal of Pediatric Genetics (2025)

pathologygenetic disordersmolecular medicinedevelopmental anomaliesnovel suclg1 variants

Feasibility of Newborn Screening for Pyridoxine-Dependent Epilepsy. Molecular Genetics and Metabolism (2024)

pediatricsgenetic disordersmolecular psychiatryepilepsy

P.48 Severe Variant for Pyridoxine Dependent Epilepsy Found in the Micronesian Population: A Case Study. Molecular Genetics and Metabolism (2024)

genetic disordersmolecular neurodegenerationmendelian disorderdisease gene identificationepilepsyhuman geneticsgenetics

Pyridoxine Dependent Epilepsy: Identification of a Founder Variant in the Micronesian Population With Severe Features. Molecular Genetics and Metabolism (2023)

genetic disordersmendelian disorderdisease gene identificationepilepsyheredityhuman geneticsmedical geneticsgenetics

Rubella Virus‐Associated Necrotizing Granulomatous Inflammation With Extensive Eyelid, Ocular, and Orbital Involvement. Pediatric Dermatology (2023)

ANABOLISM: Practical Strategies. (2022)

surgeryvascular traumavascular surgeryneuromuscular medicine

Loss of Focad, Operating via the Ski Messenger Rna Surveillance Pathway, Causes a Pediatric Syndrome With Liver Cirrhosis. Nature Genetics (2022)

disease mechanismshepatologymolecular diagnosticsmolecular biologygene expressiontranscriptomegenetics

Erin FinnKimberly KrippsChristina ChambersMichele RappNaomi J. L. MeeksFang XuWuyan ChenAustin A. LarsonNatalie J. Nokoff

pathologyadrenal diseasepathogenesisclinical investigationavian biologyclinical case reportmedicineclinical researchcase studiesgenetics

Methionine Synthase Deficiency: Variable Clinical Presentation and Benefit of Early Diagnosis and Treatment. Journal of Inherited Metabolic Disease (2021)

clinical lipidologyclinical presentationvariable clinical presentationhepatologyhematologypharmacologymedicinemethionine synthase deficiencyveterinary medicinemedical geneticshealth sciences

1
2
10 / page