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Genetic mapping

First molecular report of Moniezia expansa in small ruminants of Pakistan with epidemiological insight

Hira Muqaddas, Naunain Mehmood, [ ... ], Furhan Iqbal

TRIO RVEMVS: A Bayesian framework for rare variant association analysis with expectation-maximization variable selection using family trio data

Duo Yu, Matthew Koslovsky, [ ... ], Michael D. Swartz

Genetic structure of the commercial stingless bee Heterotrigona itama (Apidae: Meliponini) in Thailand

Kanyanat Wongsa, Ekgachai Jeratthitikul, [ ... ], Atsalek Rattanawannee

Predictors of frequency of CF care in the US Cystic Fibrosis Foundation Patient Registry

Alexandra C. Hinton, Edmund H. Sears, Jonathan B. Zuckerman, Sara Lopez-Pintado

Impact of CD40 (rs1883832) and CD40L (rs1126535) gene variants on laryngeal cancer susceptibility and their association with serum biomarker levels of sCD40 and sCD40L

Alper Gümüş, Dilara Sönmez, [ ... ], Arzu Ergen

An easy-to-use pipeline to analyze amplicon-based Next Generation Sequencing results of human mitochondrial DNA from degraded samples

Daniel R. Cuesta-Aguirre, Assumpció Malgosa, Cristina Santos

Genomic variability in Zika virus in GBS cases in Colombia

Nelson Rivera-Franco, Diana López-Alvarez, [ ... ], on behalf of NEAS

Genomic variants associated with type 2 diabetes mellitus among Filipinos

Eva Maria C. Cutiongco-de la Paz, Jose B. Nevado Jr., [ ... ], Mark David G. Francisco

Ancestral origins of TYR and OCA2 gene mutations in oculocutaneous albinism from two admixed populations in Colombia

Wilmer A. Cárdenas, Andrew B. Conley, [ ... ], María Claudia Lattig

Genome-Wide, Non-Invasive Prenatal Testing for rare chromosomal abnormalities: A systematic review and meta-analysis of diagnostic test accuracy

Marton Konya, Agnes Czimbalmos, [ ... ], Aniko Gal

Rabex-5 E3 and Rab5 GEF domains differ in their regulation of Ras, Notch, and PI3K signaling in Drosophila wing development

Theresa A. Reimels, Mia Steinberg, [ ... ], Cathie M. Pfleger

Association of variants in AGTR1, ACE, MTHFR genes with microalbuminuria and risk factors for the onset of diabetic nephropathy in adolescents with type 1 diabetes in the population of Serbia

Smiljka Kovacevic, Vera Zdravkovic, [ ... ], Maja Jesic

Genotype–phenotype analysis of hearing function in patients with DFNB1A caused by the c.-23+1G>A splice site variant of the GJB2 gene (Cx26)

Fedor M. Teryutin, Vera G. Pshennikova, [ ... ], Nikolay A. Barashkov

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