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The Kaohsiung Journal of Medical Sciences
|
January 2, 2026
Exome Sequencing Identifies Variants in MLH1 and ERBB2 as Potential Cancer-Predisposing Factors in Familial Early-Onset Colorectal Cancer
Behnaz Bagheri, Neda Mohsen-Pour, Najmeh Salehi, et al.
Biochemical Genetics
|
May 12, 2025
Novel EDARADD Variant in Ectodermal Dysplasia Unveiled by Whole-Exome Sequencing
Samira Kalayinia, Saranaz Seyed AliAkbar, Amirali Soheili, et al.
BMC Musculoskeletal Disorders
|
March 28, 2024
A novel homozygous variant (c.5876T > C: p. Leu1959Pro) in DYSF segregates with limb-girdle muscular dystrophy: a case report
Hamed Hesami, Serwa Ghasemi, Golnaz Houshmand, et al.
BMC Cardiovascular Disorders
|
August 23, 2024
Combination of FLNC and JUP variants causing arrhythmogenic cardiomyopathy in an Iranian family with different clinical features
Kasra Mehdizadeh, Mahdieh Soveizi, Amir Askarinejad, et al.
Journal of Cardiovascular and Thoracic Research
|
November 29, 2023
Polymorphism of rs599839 in the <i>PSRC1</i> gene is associated with coronary artery disease in an Iranian population
Golnaz Houshmand, Mohammad Javad Alemzadeh-Ansari, Saeideh Mazloumzadeh, et al.
BMC Medical Genomics
|
March 7, 2025
Unraveling a novel FBN1 variant in Marfan syndrome with dilated aortic root manifestation
Amirreza Sabahizadeh, Amir Askarinejad, Saranaz Seyed AliAkbar, et al.
Journal of Cellular and Molecular Medicine
|
May 15, 2023
Role of non-coding variants in cardiovascular disease
Katayoun Heshmatzad, Niloofar Naderi, Majid Maleki, et al.
Cardiology in the Young
|
November 16, 2021
Whole-exome sequencing identified compound heterozygous variants in the <i>TTN</i> gene causing Salih myopathy with dilated cardiomyopathy in an Iranian family
Mohammad Mahdavi, Neda Mohsen-Pour, Majid Maleki, et al.
Laboratory Medicine
|
May 29, 2023
Whole-exome sequencing reveals a likely pathogenic LMNA variant causing hypertrophic cardiomyopathy
Mohammad Mahdavi, Neda Mohsen-Pour, Majid Maleki, et al.
Scientific Reports
|
March 4, 2024
Exploring TTN variants as genetic insights into cardiomyopathy pathogenesis and potential emerging clues to molecular mechanisms in cardiomyopathies
Amir Ghaffari Jolfayi, Erfan Kohansal, Serwa Ghasemi, et al.
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Search research articles
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Showing results (41-50 of 53) with videos related to
Sort By:
Page
of 6
The Kaohsiung Journal of Medical Sciences
|
January 2, 2026
Exome Sequencing Identifies Variants in MLH1 and ERBB2 as Potential Cancer-Predisposing Factors in Familial Early-Onset Colorectal Cancer
Behnaz Bagheri, Neda Mohsen-Pour, Najmeh Salehi, et al.
Biochemical Genetics
|
May 12, 2025
Novel EDARADD Variant in Ectodermal Dysplasia Unveiled by Whole-Exome Sequencing
Samira Kalayinia, Saranaz Seyed AliAkbar, Amirali Soheili, et al.
BMC Musculoskeletal Disorders
|
March 28, 2024
A novel homozygous variant (c.5876T > C: p. Leu1959Pro) in DYSF segregates with limb-girdle muscular dystrophy: a case report
Hamed Hesami, Serwa Ghasemi, Golnaz Houshmand, et al.
BMC Cardiovascular Disorders
|
August 23, 2024
Combination of FLNC and JUP variants causing arrhythmogenic cardiomyopathy in an Iranian family with different clinical features
Kasra Mehdizadeh, Mahdieh Soveizi, Amir Askarinejad, et al.
Journal of Cardiovascular and Thoracic Research
|
November 29, 2023
Polymorphism of rs599839 in the <i>PSRC1</i> gene is associated with coronary artery disease in an Iranian population
Golnaz Houshmand, Mohammad Javad Alemzadeh-Ansari, Saeideh Mazloumzadeh, et al.
BMC Medical Genomics
|
March 7, 2025
Unraveling a novel FBN1 variant in Marfan syndrome with dilated aortic root manifestation
Amirreza Sabahizadeh, Amir Askarinejad, Saranaz Seyed AliAkbar, et al.
Journal of Cellular and Molecular Medicine
|
May 15, 2023
Role of non-coding variants in cardiovascular disease
Katayoun Heshmatzad, Niloofar Naderi, Majid Maleki, et al.
Cardiology in the Young
|
November 16, 2021
Whole-exome sequencing identified compound heterozygous variants in the <i>TTN</i> gene causing Salih myopathy with dilated cardiomyopathy in an Iranian family
Mohammad Mahdavi, Neda Mohsen-Pour, Majid Maleki, et al.
Laboratory Medicine
|
May 29, 2023
Whole-exome sequencing reveals a likely pathogenic LMNA variant causing hypertrophic cardiomyopathy
Mohammad Mahdavi, Neda Mohsen-Pour, Majid Maleki, et al.
Scientific Reports
|
March 4, 2024
Exploring TTN variants as genetic insights into cardiomyopathy pathogenesis and potential emerging clues to molecular mechanisms in cardiomyopathies
Amir Ghaffari Jolfayi, Erfan Kohansal, Serwa Ghasemi, et al.
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of 6