HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Jennifer Kerkhof Selected Research

RNA (Ribonucleic Acid)

1/2022OMIXCARE: OMICS technologies solved about 33% of the patients with heterogeneous rare neuro-developmental disorders and negative exome sequencing results and identified 13% additional candidate variants.
1/2022Clinical Utility of Implementing a Frontline NGS-Based DNA and RNA Fusion Panel Test for Patients with Suspected Myeloid Malignancies.
10/2019Genome-wide DNA methylation and RNA analyses enable reclassification of two variants of uncertain significance in a patient with clinical Kabuki syndrome.
9/2019Implementation of an NGS-based sequencing and gene fusion panel for clinical screening of patients with suspected hematologic malignancies.

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown:


Jennifer Kerkhof Research Topics

Disease

5Neoplasms (Cancer)
01/2023 - 10/2020
4Neurodevelopmental Disorders
01/2023 - 11/2021
3Kabuki syndrome
01/2022 - 10/2019
2Intellectual Disability (Idiocy)
02/2024 - 11/2022
2Carcinogenesis
02/2024 - 05/2023
1Rubinstein-Taybi Syndrome (Syndrome, Rubinstein-Taybi)
03/2024
1Brachydactyly
02/2024
1Cleft Palate (Palate, Cleft)
02/2024
1Autism Spectrum Disorder
02/2024
1Chromosome Fragility
11/2023
1Rare Diseases (Rare Disease)
10/2023
1Acute Myeloid Leukemia (Acute Myelogenous Leukemia)
09/2023
1Bone Marrow Failure Disorders
09/2023
1Renpenning syndrome 1
01/2023
1Disease Progression
01/2023
1Muscle Weakness
01/2023
1Duchenne Muscular Dystrophy (Muscular Dystrophy, Becker)
01/2023
1Clark-Baraitser syndrome
11/2022
1Pelger-Huet Anomaly
10/2022
1Autistic Disorder (Autism)
10/2022
1DiGeorge Syndrome (Syndrome, DiGeorge)
08/2021
1Mitochondrial Diseases (Mitochondrial Disease)
01/2021
1Adenocarcinoma
10/2020
1Hematologic Neoplasms (Hematological Malignancy)
09/2019
1Agammaglobulinemia (Hypogammaglobulinemia)
10/2018
1Free sialic acid storage disease
10/2018

Drug/Important Bio-Agent (IBA)

5ChromatinIBA
10/2022 - 08/2021
4DNA (Deoxyribonucleic Acid)IBA
11/2023 - 10/2020
4RNA (Ribonucleic Acid)IBA
01/2022 - 09/2019
3Biomarkers (Surrogate Marker)IBA
10/2023 - 01/2021
3A-Form DNA (A-DNA)IBA
01/2023 - 09/2019
2Proteins (Proteins, Gene)FDA Link
03/2024 - 02/2024
2Transcription Factors (Transcription Factor)IBA
02/2024 - 05/2023
2Poly(ADP-ribose) Polymerase InhibitorsIBA
01/2022 - 10/2020
1Retinaldehyde (Retinal)IBA
09/2023
1DystrophinIBA
01/2023
1Lysine AcetyltransferasesIBA
01/2023
1Histones (Histone)IBA
01/2023
1polyglutamine-binding protein 1IBA
01/2023
1Thyroid Hormone Receptors (Thyroid Hormone Receptor)IBA
11/2022
1ElementsIBA
11/2022
1PlatinumIBA
01/2022
1Mitochondrial DNA (mtDNA)IBA
01/2021
1Immunoglobulin G (IgG)IBA
10/2018
1N-Acetylneuraminic Acid (Sialic Acid)IBA
10/2018

Therapy/Procedure

1Therapeutics
01/2023
1Molecular Targeted Therapy
01/2023
1Drug Therapy (Chemotherapy)
01/2022