42.
Ethical, Legal, and Social Implications of Biobanks for Genetics Research
by Haga, Susanne B
Advances in Genetics, 2008, Vol.60, p.505-544

43.
Mutation effects predicted from sequence co-variation
by Hopf, Thomas A
Nature biotechnology, 2017, Vol.35 (2), p.128-135

44.
Association of Low-Frequency and Rare Coding-Sequence Variants with Blood Lipids and Coronary Heart Disease in 56,000 Whites and Blacks
by Peloso, Gina M
American journal of human genetics, 2014, Vol.94 (2), p.223-232

45.
PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses
by Purcell, Shaun
American journal of human genetics, 2007, Vol.81 (3), p.559-575

46.
The beliefs, motivations, and expectations of parents who have enrolled their children in a genetic biorepository
by Harris, Erin D
Genetics in medicine, 2012, Vol.14 (3), p.330-337

47.
Fast Principal-Component Analysis Reveals Convergent Evolution of ADH1B in Europe and East Asia
by Galinsky, Kevin J
American journal of human genetics, 2016, Vol.98 (3), p.456-472

48.
Combined Analysis of Genome-wide Association Studies for Crohn Disease and Psoriasis Identifies Seven Shared Susceptibility Loci
by Ellinghaus, David
American journal of human genetics, 2012, Vol.90 (4), p.636-647

49.
Great expectations: views of genetic research participants regarding current and future genetic studies
by Henderson, Gail
Genetics in medicine, 2008, Vol.10 (3), p.193-200

50.
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 Are Identified in Individuals with Congenital Hypogonadotropic Hypogonadism
by Miraoui, Hichem
American journal of human genetics, 2013, Vol.92 (5), p.725-743

51.
Playing a Part in Research? University Students’ Attitudes to Direct-To-Consumer Genomics
by Vayena, Effy
Community genetics, 2014, Vol.17 (3), p.158-168

52.
Examining the public refusal to consent to DNA biobanking: empirical data from a Swedish population-based study
by Melas, Philippe A
Journal of medical ethics, 2010, Vol.36 (2), p.93-98

53.
Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia
by Bogliolo, Massimo
American journal of human genetics, 2013, Vol.92 (5), p.800-806

54.
A comprehensive transcriptional portrait of human cancer cell lines
by Klijn, Christiaan
Nature biotechnology, 2015, Vol.33 (3), p.306-312

55.
Identification and development of a functional marker of TaGW2 associated with grain weight in bread wheat (Triticum aestivum L.)
by Su, Zhenqi
Theoretical and applied genetics, 2010, Vol.122 (1), p.211-223

56.
A Specific IFIH1 Gain-of-Function Mutation Causes Singleton-Merten Syndrome
by Rutsch, Frank
American journal of human genetics, 2015, Vol.96 (2), p.275-282

57.
The Expanding Landscape of Alternative Splicing Variation in Human Populations
by Park, Eddie
American journal of human genetics, 2018, Vol.102 (1), p.11-26

58.
Increasing the efficiency of precise genome editing with CRISPR-Cas9 by inhibition of nonhomologous end joining
by Maruyama, Takeshi
Nature biotechnology, 2015, Vol.33 (5), p.538-542

59.
Engineered CRISPR-Cas12a variants with increased activities and improved targeting ranges for gene, epigenetic and base editing
by Kleinstiver, Benjamin P
Nature biotechnology, 2019, Vol.37 (3), p.276-282

60.
The diploid genome sequence of an Asian individual
by Wang, Jun
Nature, 2008, Vol.456 (7218), p.60-65
