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International Journal of Molecular Sciences
|
October 14, 2023
Complexity in Genetic Epilepsies: A Comprehensive Review
Cassandra Rastin, Laila C Schenkel, Bekim Sadikovic
Journal of Pediatric Genetics
|
February 10, 2017
Constitutional Epi/Genetic Conditions: Genetic, Epigenetic, and Environmental Factors
Laila C Schenkel, David Rodenhiser, Victoria Siu, et al.
Critical Reviews in Clinical Laboratory Sciences
|
January 14, 2016
DNA methylation analysis in constitutional disorders: Clinical implications of the epigenome
Laila C Schenkel, David I Rodenhiser, Peter J Ainsworth, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
July 19, 2023
Genotypic analysis of a large cohort of patients with suspected atypical hemolytic uremic syndrome
Dervla M Connaughton, Pratibha Bhai, Paul Isenring, et al.
The Journal of Nutritional Biochemistry
|
August 6, 2015
Choline supplementation restores substrate balance and alleviates complications of Pcyt2 deficiency
Laila C Schenkel, Sugashan Sivanesan, Junzeng Zhang, et al.
The Journal of Molecular Diagnostics : JMD
|
September 2, 2016
Clinical Validation of Fragile X Syndrome Screening by DNA Methylation Array
Laila C Schenkel, Charles Schwartz, Cindy Skinner, et al.
Genes
|
November 11, 2022
Evaluation of DNA Methylation Array for Glioma Tumor Profiling and Description of a Novel Epi-Signature to Distinguish IDH1/IDH2 Mutant and Wild-Type Tumors
Laila C Schenkel, Joseph Mathew, Hal Hirte, et al.
JCEM Case Reports
|
February 5, 2025
A Novel and Rare Pathogenic Gene Variant in 2 Patients With Multiple Endocrine Neoplasia Type 1 (MEN-1) Syndrome
Jordan C LeSarge, Hani Rjoob, Kristin K Clemens, et al.
Frontiers in Oncology
|
May 10, 2018
Genomic DNA Methylation-Derived Algorithm Enables Accurate Detection of Malignant Prostate Tissues
Erfan Aref-Eshghi, Laila C Schenkel, Peter Ainsworth, et al.
Epigenetics
|
September 22, 2017
The defining DNA methylation signature of Kabuki syndrome enables functional assessment of genetic variants of unknown clinical significance
Erfan Aref-Eshghi, Laila C Schenkel, Hanxin Lin, et al.
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of 3
Search research articles
Search
Showing results (1-10 of 22) with videos related to
Sort By:
Page
of 3
International Journal of Molecular Sciences
|
October 14, 2023
Complexity in Genetic Epilepsies: A Comprehensive Review
Cassandra Rastin, Laila C Schenkel, Bekim Sadikovic
Journal of Pediatric Genetics
|
February 10, 2017
Constitutional Epi/Genetic Conditions: Genetic, Epigenetic, and Environmental Factors
Laila C Schenkel, David Rodenhiser, Victoria Siu, et al.
Critical Reviews in Clinical Laboratory Sciences
|
January 14, 2016
DNA methylation analysis in constitutional disorders: Clinical implications of the epigenome
Laila C Schenkel, David I Rodenhiser, Peter J Ainsworth, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
July 19, 2023
Genotypic analysis of a large cohort of patients with suspected atypical hemolytic uremic syndrome
Dervla M Connaughton, Pratibha Bhai, Paul Isenring, et al.
The Journal of Nutritional Biochemistry
|
August 6, 2015
Choline supplementation restores substrate balance and alleviates complications of Pcyt2 deficiency
Laila C Schenkel, Sugashan Sivanesan, Junzeng Zhang, et al.
The Journal of Molecular Diagnostics : JMD
|
September 2, 2016
Clinical Validation of Fragile X Syndrome Screening by DNA Methylation Array
Laila C Schenkel, Charles Schwartz, Cindy Skinner, et al.
Genes
|
November 11, 2022
Evaluation of DNA Methylation Array for Glioma Tumor Profiling and Description of a Novel Epi-Signature to Distinguish IDH1/IDH2 Mutant and Wild-Type Tumors
Laila C Schenkel, Joseph Mathew, Hal Hirte, et al.
JCEM Case Reports
|
February 5, 2025
A Novel and Rare Pathogenic Gene Variant in 2 Patients With Multiple Endocrine Neoplasia Type 1 (MEN-1) Syndrome
Jordan C LeSarge, Hani Rjoob, Kristin K Clemens, et al.
Frontiers in Oncology
|
May 10, 2018
Genomic DNA Methylation-Derived Algorithm Enables Accurate Detection of Malignant Prostate Tissues
Erfan Aref-Eshghi, Laila C Schenkel, Peter Ainsworth, et al.
Epigenetics
|
September 22, 2017
The defining DNA methylation signature of Kabuki syndrome enables functional assessment of genetic variants of unknown clinical significance
Erfan Aref-Eshghi, Laila C Schenkel, Hanxin Lin, et al.
Page
of 3