Maryam Rezaei
Montreal, QC, Canada
Last Updated: 09/26/2026
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Found 12 publications
Lessons learned from the exome sequencing of nine cases of infertility and the way forward.
Journal: Reproductive biomedicine online
Published: July 28, 2025
Defects in meiosis I contribute to the genesis of androgenetic hydatidiform moles.
Journal: The Journal of clinical investigation
Published: March 21, 2023
Functionally Assessing the Age-Related Decline in the Detection Rate of Photons by Cone Photoreceptors.
Journal: Frontiers in aging neuroscience
Published: July 20, 2021
Evaluation of Cognitive Impairment in Refractory Temporal Lobe Epilepsy Patients Concerning Structural Brain Lesions.
Journal: Basic and clinical neuroscience
Published: July 02, 2021
A protein-truncating mutation in CCNB3 in a patient with recurrent miscarriages and failure of meiosis I.
Journal: Journal of medical genetics
Published: March 25, 2021
Novel pathogenic variants in NLRP7, NLRP5, and PADI6 in patients with recurrent hydatidiform moles and reproductive failure.
Journal: Clinical genetics
Published: January 25, 2021
The genetics of recurrent hydatidiform moles in Mexico: further evidence of a strong founder effect for one mutation in NLRP7 and its widespread.
Journal: Journal of assisted reproduction and genetics
Published: January 01, 2021
Biallelic PADI6 variants linking infertility, miscarriages, and hydatidiform moles.
Journal: European journal of human genetics : EJHG
Published: December 05, 2017
The genetics of recurrent hydatidiform moles: new insights and lessons from a comprehensive analysis of 113 patients.
Journal: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
Published: November 23, 2017
The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions.
The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions.
Journal: European journal of human genetics : EJHG
Published: September 16, 2016
Two novel mutations in the KHDC3L gene in Asian patients with recurrent hydatidiform mole.
Journal: Human genome variation
Published: December 17, 2015
The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions.
The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions.
Journal: European journal of human genetics : EJHG
Published: September 22, 2015
Showing 1-12 of 12
Last Updated: 09/26/2026