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The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
August 14, 2023
Congenital Myopathy Due to Pathogenic Missense Variant in the <i>MYBPC1</i> Gene
Vinaya Bhandari, Raymond Kim, Hanna Faghfoury, et al.
Molecular Biology and Evolution
|
June 12, 2014
Neanderthal origin of the haplotypes carrying the functional variant Val92Met in the MC1R in modern humans
Qiliang Ding, Ya Hu, Shuhua Xu, et al.
International Journal of Molecular Sciences
|
August 10, 2024
Accurate and Automated Genotyping of the <i>CFTR</i> Poly-T/TG Tract with <i>CFTR</i>-TIPS
Qiliang Ding, Christopher D Hofich, Tifani B Kellogg, et al.
Clinical Epigenetics
|
April 29, 2025
Thirteen cases support the clinical significance of imprinting center 1 (IC1) microdeletions in Beckwith-Wiedemann syndrome
Qiliang Ding, Zinandre Stander, Brandon J Elizalde, et al.
Molecular Cytogenetics
|
November 13, 2024
False-positive XXY results by interphase FISH in cytogenetically normal XX individuals: two cases highlighting the necessity of additional laboratory follow-up
Qiliang Ding, Abigail L Bronson, Kyna A Byerly, et al.
Prenatal Diagnosis
|
April 11, 2025
Artifacts, Not Differences in Sex Development, Are the Predominant Cause of Phenotypic Sex Discordance With Prenatal Cell-Free DNA Screening: A Review of 33 Cases
Qiliang Ding, Nicole L Hoppman, Erik C Thorland, et al.
Hematology Reports
|
April 27, 2026
Concomitant Clonal <i>CBFB</i>::<i>MYH11</i> and <i>PDGFRB</i> Fusions in a Case of <i>De Novo</i> Acute Myeloid Leukemia
Qiliang Ding, Natasha E Lewis, Cody J Artymiuk, et al.
Familial Cancer
|
July 22, 2023
Germline whole genome sequencing in adults with multiple primary tumors
Yiming Wang, Qiliang Ding, Stephenie Prokopec, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 4, 2025
Rethinking the pathogenicity of intragenic DMD duplications detected by carrier screening: High prevalence of nontandem duplications revealed by long-read sequencing
Qiliang Ding, Jagadheshwar Balan, Noemi Vidal-Folch, et al.
American Journal of Clinical Pathology
|
February 10, 2025
Follow the LINE: A novel case of dilated cardiomyopathy caused by a LINE-1 insertion in the TTN gene
Qiliang Ding, Jenna Fine, Frank T Hoffman, et al.
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Search research articles
Search
Showing results (11-20 of 27) with videos related to
Sort By:
Page
of 3
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
August 14, 2023
Congenital Myopathy Due to Pathogenic Missense Variant in the <i>MYBPC1</i> Gene
Vinaya Bhandari, Raymond Kim, Hanna Faghfoury, et al.
Molecular Biology and Evolution
|
June 12, 2014
Neanderthal origin of the haplotypes carrying the functional variant Val92Met in the MC1R in modern humans
Qiliang Ding, Ya Hu, Shuhua Xu, et al.
International Journal of Molecular Sciences
|
August 10, 2024
Accurate and Automated Genotyping of the <i>CFTR</i> Poly-T/TG Tract with <i>CFTR</i>-TIPS
Qiliang Ding, Christopher D Hofich, Tifani B Kellogg, et al.
Clinical Epigenetics
|
April 29, 2025
Thirteen cases support the clinical significance of imprinting center 1 (IC1) microdeletions in Beckwith-Wiedemann syndrome
Qiliang Ding, Zinandre Stander, Brandon J Elizalde, et al.
Molecular Cytogenetics
|
November 13, 2024
False-positive XXY results by interphase FISH in cytogenetically normal XX individuals: two cases highlighting the necessity of additional laboratory follow-up
Qiliang Ding, Abigail L Bronson, Kyna A Byerly, et al.
Prenatal Diagnosis
|
April 11, 2025
Artifacts, Not Differences in Sex Development, Are the Predominant Cause of Phenotypic Sex Discordance With Prenatal Cell-Free DNA Screening: A Review of 33 Cases
Qiliang Ding, Nicole L Hoppman, Erik C Thorland, et al.
Hematology Reports
|
April 27, 2026
Concomitant Clonal <i>CBFB</i>::<i>MYH11</i> and <i>PDGFRB</i> Fusions in a Case of <i>De Novo</i> Acute Myeloid Leukemia
Qiliang Ding, Natasha E Lewis, Cody J Artymiuk, et al.
Familial Cancer
|
July 22, 2023
Germline whole genome sequencing in adults with multiple primary tumors
Yiming Wang, Qiliang Ding, Stephenie Prokopec, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 4, 2025
Rethinking the pathogenicity of intragenic DMD duplications detected by carrier screening: High prevalence of nontandem duplications revealed by long-read sequencing
Qiliang Ding, Jagadheshwar Balan, Noemi Vidal-Folch, et al.
American Journal of Clinical Pathology
|
February 10, 2025
Follow the LINE: A novel case of dilated cardiomyopathy caused by a LINE-1 insertion in the TTN gene
Qiliang Ding, Jenna Fine, Frank T Hoffman, et al.
Page
of 3