Jannah Shamsani

ID Genomics (United States) — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

8h-index258citations12works9.02yr avg
OpenAlex↗ORCID↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

RNA Research and Splicing(4), Amyotrophic Lateral Sclerosis Research(3), Cancer Genomics and Diagnostics(3), Genetic factors in colorectal cancer(3), Genomics and Rare Diseases(3)

Publications12 total

Amyotrophic lateral sclerosis diagnosis using machine learning and multi-omic data integration
Heliyon·2024· 9 citedOpen Access
Novel variants in established epilepsy genes in focal epilepsy
Seizure·2023· 3 citedOpen Access
Novel GATOR1 variants in focal epilepsy
Epilepsy & Behavior·2023· 8 cited
Molecular Classification and Interpretation of Amyotrophic Lateral Sclerosis Using Deep Convolution Neural Networks and Shapley Values
Genes·2021· 20 citedOpen Access
Molecular Classification and Interpretation of Amyotrophic Lateral Sclerosis Using Deep Convolution Neural Networks and Shapley Values
Preprints.org·2021· 3 citedOpen Access
Tumor Signature Analysis Implicates Hereditary Cancer Genes in Endometrial Cancer Development
Cancers·2021· 8 citedOpen Access
Identification of genetic variants associated with risk of endometrial cancer
2020
A plugin for the Ensembl Variant Effect Predictor that uses MaxEntScan to predict variant spliceogenicity
Bioinformatics·2018· 86 citedOpen Access
Endometrial cancer gene panels: clinical diagnostic vs research germline DNA testing
Modern Pathology·2017· 60 citedOpen Access
The Association of CYP19A1 Variation with Circulating Estradiol and Aromatase Inhibitor Outcome: Can CYP19A1 Variants Be Used to Predict Treatment Efficacy?
Frontiers in Pharmacology·2017· 7 citedOpen Access
Frequent occurrence of gastric cancer in Asian kindreds with Li–Fraumeni syndrome
Clinical Genetics·2014· 17 cited
Whole-genome sequencing analysis of phenotypic heterogeneity and anticipation in Li–Fraumeni cancer predisposition syndrome
Proceedings of the National Academy of Sciences·2014· 37 citedOpen Access

Frequent Co-authors

Amanda B. Spurdle(4), Tracy A. O’Mara(3), Abdul Karim(3), Zheng Su(3), Ognjen Milićević(3), Hima Nikafshan Rad(3), Nicola Waddell(2), Judy Kirk(2), Hany Ariffin(2), Pierre Hainaut(2), Adelyne Chan(2), Mawar Karsa(2), Phillip K. West(2), Matthew Keon(2), Samuel Brennan(2), Ted Wong(2), Guus Teunisse(2), Maša Kovačević(2), Milena Janković(2), Marija Branković(2)