PPARdelta in humans: genetic and pharmacological evidence for a significant metabolic function. by Karpe, F, Ehrenborg, E

HUMAN GENETIC POLYMORPHISMS AND THE RISK OF MALARIA-ASSOCIATED SEIZURES IN AFRICAN POPULATIONS by Kariuki, S, Rockett, K, Clark, T, Reyburn, H, Agbenyega, T, Taylor, T, Williams, T, Newton, C

Structures of CUG repeats in RNA. Potential implications for human genetic diseases. by Pinheiro, P, Scarlett, G, Rodger, A, Rodger, P, Murray, A, Brown, T, Newbury, S, McClellan, J

“…Triplet repeats that cause human genetic diseases have been shown to exhibit unusual compact structures in DNA, and in this paper we show that similar structures exist in shorter "normal length" CNG RNA. …”

Searching for the human genetic factors standing in the way of universally effective vaccines. by Mentzer, A, O'Connor, D, Pollard, A, Hill, A

“…There is compelling evidence that a significant proportion of this variability can be attributed to human genetic variation, especially for those vaccines administered in early life. …”

A second update on mapping the human genetic architecture of COVID-19 by Kanai, M, Andrews, SJ, Cordioli, M, COVID-19 Host Genetics Initiative, Malinauskas, T, Elliott, K, Knight, J, Wilson, D, Earle, SG, Lin, S, Arning, N, Armstrong, J, Rudkin, JK, Crook, D, Wyllie, DH, Band, G

Mendelian randomization as a tool to inform drug development using human genetics by Iyas Daghlas, Dipender Gill

“…A promising strategy for expediting and improving the probability of success in the drug development process is the use of naturally randomized human genetic variation for drug target identification and validation. …”
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Studying the factors affecting human genetics due to environmental degradation and climate change by Mirsaidova Khilola, Iskandarova Viktoriya, Sattarova Zebo

“…Environmental degradation and climate change have significant impacts on human genetics. The article examines the factors affecting human genetics due to these changes. …”
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Combining Human Genetics of Multiple Sclerosis with Oxidative Stress Phenotype for Drug Repositioning by Stefania Olla, Maristella Steri, Alessia Formato, Michael B. Whalen, Silvia Corbisiero, Cristina Agresti

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Human genetics as a model for target validation: finding new therapies for diabetes by Thomsen, S, Gloyn, A

“…These findings highlight the potential for use of human genetic variation for prospective target validation, and establish a framework for future applications. …”

Human genetics of obesity and type 2 diabetes mellitus: past, present, and future by Ingelsson, E, McCarthy, M

“…We highlight obstacles to the translation of human genetic findings into mechanism inference but are optimistic that, as these are overcome, there is untapped potential for novel drugs and more effective strategies for treating and preventing T2D and obesity.…”

Flow cytogenetics/ by Gray, Joe W.

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Science and the question of human equality / by Collins, Margaret S.

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Molecular sensors for cardiovascular homeostasis / [electronic resource] by 228836 Wang, Donna H., SpringerLink (Online service)

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Evolutionary genomics : statistical and computational methods / by Anisimova, Maria

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Inheritance : how our genes change our lives / by 299867 Moalem, Sharon author, LaPlante, Matthew D author

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Computational Biology of Non-Coding RNA : Methods and Protocols / by Lai, Xin, editor 636268, Gupta, Shailendra Kumar, editor 636269, Vera, Julio, editor 636270

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New insights from GWAS on BMI-related growth traits in a longitudinal cohort of admixed children with Native American and European ancestry by Lucas Vicuña, Esteban Barrientos, Tomás Norambuena, Danilo Alvares, Juan Cristobal Gana, Valeria Leiva-Yamaguchi, Cristian Meza, José L. Santos, Veronica Mericq, Ana Pereira, Susana Eyheramendy

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The fragile X locus is prone to spontaneous DNA damage that is preferentially repaired by nonhomologous end-joining to preserve genome integrity by Daman Kumari, Rachel Adihe Lokanga, Cai McCann, Thomas Ried, Karen Usdin

Subjects: “…Human Genetics…”
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Mutational burden of XPNPEP3 leads to defects in mitochondrial complex I and cilia in NPHPL1 by Lingxiao Tong, Jia Rao, Chenxi Yang, Jie Xu, Yijun Lu, Yuchen Zhang, Xiaohui Cang, Shanshan Xie, Jianhua Mao, Pingping Jiang

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Genetic identification of members of the prominent Báthory aristocratic family by Alexandra Gînguță, Bence Kovács, Oszkár Schütz, Balázs Tihanyi, Emil Nyerki, Kitti Maár, Zoltán Maróti, Gergely I.B. Varga, Dan Băcueț-Crișan, Timea Keresztes, Tibor Török, Endre Neparáczki

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