Abdul Noor

Biochemistry, Genetics and Molecular Biology · Life Sciences

30h-index8.0kcitations99works0.72yr avg
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Research Topics

Genomic variations and chromosomal abnormalities(33), Genomics and Rare Diseases(27), Genetics and Neurodevelopmental Disorders(25), Prenatal Screening and Diagnostics(13), Autism Spectrum Disorder Research(11)

Publications99 total

Findings from Comprehensive Genome Sequencing in the Canadian Population: Results from the GENCOV Study
Genetics in Medicine Open·2026Open Access
Opportunistic screening for broad range of medically relevant secondary findings: Laboratory benefits and burdens
Genetics in Medicine·2025Open Access
P867: A cautionary tale of fetoplacental discrepancies: The impact of mosaicism in prenatal diagnosis
Genetics in Medicine Open·2025Open Access
Effect of Different Root Stocks on Kaghzi Lime During First Year of Growth and Insecticidal Suppression of Citrus Leafminer
Sarhad Journal of Agriculture·2025Open Access
P686: Opportunistic screening for broad range of clinically relevant secondary findings: Outcomes of exome analysis in the Incidental Genomics RCT
Genetics in Medicine Open·2025Open Access
P298: Decoding ambiguity: Evaluating the psychological harms and utility of returning cancer variants of uncertain significance
Genetics in Medicine Open·2025Open Access
Clinical Utility of Genomic Sequencing for Hereditary Cancer Syndromes: An Observational Cohort Study
JCO Precision Oncology·2024· 1 cited
Persistent Hyperinsulinemic Hypoglycemia of Infancy: A Clinical Case Report
Clinical Research·2024Open Access
Opportunistic genomic screening has clinical utility: An interventional cohort study
Genetics in Medicine·2024· 5 citedOpen Access
Validation of low‐pass genome sequencing for prenatal diagnosis
Prenatal Diagnosis·2024· 6 citedOpen Access
P555: Clinical utility returning of all types of medically relevant genomic sequencing findings: An observational study
Genetics in Medicine Open·2024Open Access
P523: Returning all clinically relevant findings from genomic sequencing: Preliminary results from the incidental genomics RCT
Genetics in Medicine Open·2024Open Access
P709: Self reported vs genetic ancestry from the GENCOV COVID-19 genomic sequencing study
Genetics in Medicine Open·2024Open Access
P782: Validation of low-pass genome sequencing for prenatal diagnosis
Genetics in Medicine Open·2024Open Access
P574: Summary of findings from comprehensive genome sequencing performed in a healthy population cohort*
Genetics in Medicine Open·2024Open Access
P769: Trio-whole exome and whole genome sequencing in fetal central nervous system anomalies
Genetics in Medicine Open·2024Open Access
P733: Comparative analysis of DNA variant classifications between the GENCOV COVID-19 genome study and the ClinVar database
Genetics in Medicine Open·2024Open Access
P710: Phenome-wide association study (PheWAS) for the Canadian HostSeq Biobank
Genetics in Medicine Open·2024Open Access
Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta‐analysis
Prenatal Diagnosis·2023· 22 citedOpen Access
Characterizing Risk Factors for Hospitalization and Clinical Characteristics in a Cohort of COVID-19 Patients Enrolled in the GENCOV Study
Viruses·2023· 7 citedOpen Access
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Frequent Co-authors

John B. Vincent(24), Stephen W. Scherer(16), Christian R. Marshall(13), Muhammad Ayub(10), Christian Windpassinger(10), Wendy Roberts(8), Muhammad Rafiq(8), Dimitri J. Stavropoulos(8), Bridget A. Fernandez(7), Anath C. Lionel(7), David Chitayat(7), Muhammad Ansar(7), Dalila Pinto(5), Farooq Naeem(5), Marsha Speevak(5), Anna Mikhailov(5), Daniele Merico(4), Rosanna Weksberg(4), Bhooma Thiruvahindrapuram(4), Erwin Petek(4)