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Academic Journal

Population structure in genetic studies: Confounding factors and mixed models.

Authors : Sul, Jae Hoon¹; Martin, Lana S.²; Eskin, Eleazar^2,3

Source: PLoS Genetics. 12/27/2018, Vol. 14 Issue 12, p1-22. 22p.

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Academic Journal

Acquisition and transfer of antibiotic resistance genes in association with conjugative plasmid or class 1 integrons of Acinetobacter baumannii.

Authors : Leungtongkam, Udomluk¹; Thummeepak, Rapee¹; Tasanapak, Kannipa¹

Source: PLoS ONE. 12/6/2018, Vol. 13 Issue 12, p1-12. 12p.

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Academic Journal

Impact of variants on type-2 diabetes risk genes identified through genomewide association studies in polycystic ovary syndrome: a case-control study.

Authors : Ezzidi, Intissar^1,2 ; Mtiraoui, Nabil^1,2; Mohmmed Ali, Mohammed Eltigani³

Source: Journal of Genetics. Dec2018, Vol. 97 Issue 5, p1213-1223. 11p.

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Academic Journal

Relationship between the genetic expression of WTAP and bladder cancer and patient prognosis.

Authors : Chen, Lezhong; Wang, Xinghuan

Source: Oncology Letters. Dec2018, Vol. 16 Issue 6, p6966-6970. 5p.

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Academic Journal

Mouse genome-wide association studies and systems genetics uncover the genetic architecture associated with hepatic pharmacokinetic and pharmacodynamic properties of a constrained ethyl antisense oligonucleotide targeting Malat1.

Authors : Pirie, Elaine¹; Ray, Shayoni¹; Pan, Calvin²

Source: PLoS Genetics. 10/29/2018, Vol. 14 Issue 10, p1-22. 22p.

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Academic Journal

Reflection of Scholarly Communications on Journal of Genetics: A Bibliometrics Study.

Authors : Kavitha, E. S.¹

Source: Asian Journal of Information Science & Technology (AJIST). Oct-Dec2018, Vol. 8 Issue 3, p32-40. 9p.

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Academic Journal

Genetic association of ADIPOQ gene variants (-3971A>G and +276G>T) with obesity and metabolic syndrome in North Indian Punjabi population.

Authors : Kaur, Harjit¹; Badaruddoza, Badaruddoza¹ ; Bains, Veena¹

Source: PLoS ONE. 9/28/2018, Vol. 13 Issue 9, p1-17. 17p.

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Academic Journal

Quantification of dysarthrοphonia in a Cypriot family with autosomal recessive hereditary spastic paraplegia associated with a homozygous SPG11 mutation.

Authors : Konstantopoulos, Kostas^1,2 ; Zamba-Papanicolaou, Eleni^2,3 ; Christodoulou, Kyproula^3,4

Source: Neurological Sciences. Sep2018, Vol. 39 Issue 9, p1547-1550. 4p. 2 Charts.

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Academic Journal

Clinical genetics and genomic medicine in Qatar.

Authors : Al‐Dewik, Nader¹; Al‐Mureikhi, Mariam¹; Shahbeck, Noora¹

Source: Molecular Genetics & Genomic Medicine. Sep2018, Vol. 6 Issue 5, p702-712. 11p.

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Academic Journal

Establishment of the Alabama Hereditary Cancer Cohort ‐ strategies for the inclusion of underrepresented populations in cancer genetics research.

Authors : Bishop, Madison R.^1,2; Shah, Amit¹; Shively, Melissa¹

Source: Molecular Genetics & Genomic Medicine. Sep2018, Vol. 6 Issue 5, p766-778. 13p.

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