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Academic Journal

EPHA4 Genetic Variant in a Patient with Epilepsy, Ophthalmological Anomalies, and Neurodevelopmental Delay.

Authors : Sleptsova, M^1,2 (AUTHOR) ; Georgiev, C³ (AUTHOR); Atemin, S¹ (AUTHOR)

Source: Balkan Journal of Medical Genetics. Dec2023, Vol. 26 Issue 2, p65-68. 4p.

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Genetic Variant HLA-DRB1*0403 and Therapeutic Response to Disease-Modifying Therapies in Multiple Sclerosis: A Case-Control Study.

Authors : Gomez-Gaitan, Esteban Alejandro¹ (AUTHOR) ; Garcia-Ortega, Yessica Eleanet² (AUTHOR) ; Saldaña-Cruz, Ana Miriam³ (AUTHOR)

Source: International Journal of Molecular Sciences. Oct2023, Vol. 24 Issue 19, p14594. 9p.

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Vitamin D receptor genetic variant associated with asthma in Swedish school‐children.

Authors : Filiou, Anastasia^1,2 (AUTHOR) ; Hoyer, Angela^1,2 (AUTHOR); Holmdahl, Idun^1,2 (AUTHOR)

Source: Clinical & Experimental Allergy. Oct2023, Vol. 53 Issue 10, p1045-1049. 5p. 1 Diagram, 1 Graph.

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Association between the genetic variant in the vitamin D pathway (rs2282679), circulating 25-hydroxyvitamin D levels, insulin resistance and metabolic syndrome criteria.

Authors : de Luis, Daniel¹ ; Izaola, Olatz¹; Primo, David¹

Source: Nutrición Hospitalaria. nov/dic2023, Vol. 40 Issue 6, p1176-1182. 7p.

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PNPLA3 rs738409 Genetic Variant Inversely Correlates with Platelet Count, Thereby Affecting the Performance of Noninvasive Scores of Hepatic Fibrosis.

Authors : Meroni, Marica¹ (AUTHOR) ; Dongiovanni, Paola¹ (AUTHOR)

Source: International Journal of Molecular Sciences. Oct2023, Vol. 24 Issue 20, p15046. 8p.

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C-Reactive Protein Level and the Genetic Variant rs1130864 in the CRP Gene as Prognostic Factors for 10-Year Cardiovascular Outcome.

Authors : Schulz, Susanne¹ (AUTHOR) ; Rehm, Selina¹ (AUTHOR) ; Schlitt, Axel^2,3 (AUTHOR)

Source: Cells (2073-4409). Jul2023, Vol. 12 Issue 13, p1775. 12p.

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PSReliP: an integrated pipeline for analysis and visualization of population structure and relatedness based on genome-wide genetic variant data.

Authors : Solovieva, Elena¹ (AUTHOR); Sakai, Hiroaki¹ (AUTHOR)

Source: BMC Bioinformatics. 4/5/2023, Vol. 24 Issue 1, p1-22. 22p.

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A Novel Genetic Variant in MBD5 Associated with Severe Epilepsy and Intellectual Disability: Potential Implications on Neural Primary Cilia.

Authors : Martins, Mariana^1,2 (AUTHOR); Oliveira, Ana Rafaela¹ (AUTHOR); Martins, Solange^1,3 (AUTHOR)

Source: International Journal of Molecular Sciences. Aug2023, Vol. 24 Issue 16, p12603. 16p.

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Programmed cell death 1 genetic variant and liver damage in nonalcoholic fatty liver disease.

Authors : Pipitone, Rosaria M.¹ (AUTHOR); Malvestiti, Francesco² (AUTHOR); Pennisi, Grazia¹ (AUTHOR)

Source: Liver International. Aug2023, Vol. 43 Issue 8, p1761-1771. 11p. 2 Charts, 4 Graphs.

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Prevalence of CCR5 Delta 32 Genetic Variant in the Turkmen Population of Golestan Province, Northeast of Iran.

Authors : Norasi, Elmira¹ (AUTHOR); Rastegar, Mostafa² (AUTHOR); Hosseini, Seyedeh Delafruz³ (AUTHOR)

Source: BioMed Research International. 6/21/2023, p1-8. 8p.

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فلترة النتائج

EPHA4 Genetic Variant in a Patient with Epilepsy, Ophthalmological Anomalies, and Neurodevelopmental Delay.

Genetic Variant HLA-DRB1*0403 and Therapeutic Response to Disease-Modifying Therapies in Multiple Sclerosis: A Case-Control Study.

Vitamin D receptor genetic variant associated with asthma in Swedish school‐children.

Association between the genetic variant in the vitamin D pathway (rs2282679), circulating 25-hydroxyvitamin D levels, insulin resistance and metabolic syndrome criteria.

PNPLA3 rs738409 Genetic Variant Inversely Correlates with Platelet Count, Thereby Affecting the Performance of Noninvasive Scores of Hepatic Fibrosis.

C-Reactive Protein Level and the Genetic Variant rs1130864 in the CRP Gene as Prognostic Factors for 10-Year Cardiovascular Outcome.

PSReliP: an integrated pipeline for analysis and visualization of population structure and relatedness based on genome-wide genetic variant data.

A Novel Genetic Variant in MBD5 Associated with Severe Epilepsy and Intellectual Disability: Potential Implications on Neural Primary Cilia.

Programmed cell death 1 genetic variant and liver damage in nonalcoholic fatty liver disease.

Prevalence of CCR5 Delta 32 Genetic Variant in the Turkmen Population of Golestan Province, Northeast of Iran.

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