163.
A One-Penny Imputed Genome from Next-Generation Reference Panels
by Browning, Brian L
American journal of human genetics, 2018, Vol.103 (3), p.338-348

164.
Confronting real time ethical, legal, and social issues in the Electronic Medical Records and Genomics (eMERGE) Consortium
by Clayton, Ellen Wright
Genetics in medicine, 2010, Vol.12 (10), p.616-620

165.
StringTie enables improved reconstruction of a transcriptome from RNA-seq reads
by Pertea, Mihaela
Nature biotechnology, 2015, Vol.33 (3), p.290-295

166.
A genomic perspective on HLA evolution
by Meyer, Diogo
Immunogenetics (New York), 2017, Vol.70 (1), p.5-27

167.
Sequence-specific antimicrobials using efficiently delivered RNA-guided nucleases
by Citorik, Robert J
Nature biotechnology, 2014, Vol.32 (11), p.1141-1145

168.
Whole-genome sequencing of quartet families with autism spectrum disorder
by Yuen, Ryan K C
Nature medicine, 2015, Vol.21 (2), p.185-191

169.
Visualization of Genetic Drift Processes Using the Conserved Collagen 1[alpha]1 GXY Domain
by Kleinnijenhuis, Anne J
Journal of molecular evolution, 2019, Vol.87 (2-3), p.106

170.
Genetic associations in diabetic nephropathy: a meta-analysis
by Mooyaart, A. L
Diabetologia, 2010, Vol.54 (3), p.544-553

171.
Consideration of Cosegregation in the Pathogenicity Classification of Genomic Variants
by Jarvik, Gail P
American journal of human genetics, 2016, Vol.98 (6), p.1077-1081

172.
A “Copernican” Reassessment of the Human Mitochondrial DNA Tree from its Root
by Behar, Doron M
American journal of human genetics, 2012, Vol.90 (4), p.675-684

173.
Messenger RNA Degradation in Bacterial Cells
by Hui, Monica P
Annual review of genetics, 2014, Vol.48 (1), p.537-559

174.
Allelic Skewing of DNA Methylation Is Widespread across the Genome
by Schalkwyk, Leonard C
American journal of human genetics, 2010, Vol.86 (2), p.196-212

175.
Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort
by Waszak, Sebastian M
The lancet oncology, 2018, Vol.19 (6), p.785-798

176.
Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol
by Schmidt, Ellen M
American journal of human genetics, 2014, Vol.94 (2), p.233-245

177.
Sequencing wild and cultivated cassava and related species reveals extensive interspecific hybridization and genetic diversity
by Bredeson, Jessen V
Nature biotechnology, 2016, Vol.34 (5), p.562-570

178.
Haploinsufficiency of a Spliceosomal GTPase Encoded by EFTUD2 Causes Mandibulofacial Dysostosis with Microcephaly
by Lines, Matthew A
American journal of human genetics, 2012, Vol.90 (2), p.369-377

179.
Increased l1 retrotransposition in the neuronal genome in schizophrenia
by Bundo, Miki
Neuron (Cambridge, Mass.), 2014, Vol.81 (2), p.306-313

180.
The historical role of species from the Solanaceae plant family in genetic research
by Gebhardt, Christiane
Theoretical and Applied Genetics, 2016, Vol.129 (12), p.2281-2294
