41.
Fast Principal-Component Analysis Reveals Convergent Evolution of ADH1B in Europe and East Asia
by Galinsky, Kevin J
American journal of human genetics, 2016-03-03, Vol.98 (3), p.456-472

42.
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, 2012-04-06, Vol.90 (4), p.636-647

43.
Great expectations: views of genetic research participants regarding current and future genetic studies
by Henderson, Gail
Genetics in medicine, 2008-03, Vol.10 (3), p.193-200

44.
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 Are Identified in Individuals with Congenital Hypogonadotropic Hypogonadism
by Miraoui, Hichem
American journal of human genetics, 2013-05-02, Vol.92 (5), p.725-743

45.
Playing a Part in Research? University Students’ Attitudes to Direct-To-Consumer Genomics
by Vayena, Effy
Community genetics, 2014-01-01, Vol.17 (3), p.158-168

46.
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, 2010-02, Vol.36 (2), p.93-98

47.
Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia
by Bogliolo, Massimo
American journal of human genetics, 2013-05-02, Vol.92 (5), p.800-806

48.
A comprehensive transcriptional portrait of human cancer cell lines
by Klijn, Christiaan
Nature biotechnology, 2015-03, Vol.33 (3), p.306-312

49.
A Specific IFIH1 Gain-of-Function Mutation Causes Singleton-Merten Syndrome
by Rutsch, Frank
American journal of human genetics, 2015-02-05, Vol.96 (2), p.275-282

50.
The Expanding Landscape of Alternative Splicing Variation in Human Populations
by Park, Eddie
American journal of human genetics, 2018-01-04, Vol.102 (1), p.11-26

51.
Engineered CRISPR-Cas12a variants with increased activities and improved targeting ranges for gene, epigenetic and base editing
by Kleinstiver, Benjamin P
Nature biotechnology, 2019-03, Vol.37 (3), p.276-282

52.
The diploid genome sequence of an Asian individual
by Wang, Jun
Nature, 2008-11-06, Vol.456 (7218), p.60-65

53.
The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities
by Chong, Jessica X
American journal of human genetics, 2015-08-06, Vol.97 (2), p.199-215

54.
Common genetic variants on 5p14.1 associate with autism spectrum disorders
by Hakonarson, Hakon
Nature, 2009-05-28, Vol.459 (7246), p.528-533

55.
How anonymous is ‘anonymous’? Some suggestions towards a coherent universal coding system for genetic samples
by Schmidt, Harald
Journal of medical ethics, 2012-05, Vol.38 (5), p.304-309

56.
DNA methylation-based classification and grading system for meningioma: a multicentre, retrospective analysis
by Sahm, Felix, MD
The lancet oncology, 2017, Vol.18 (5), p.682-694

57.
Mutations in DDX58, which Encodes RIG-I, Cause Atypical Singleton-Merten Syndrome
by Jang, Mi-Ae
American journal of human genetics, 2015-02-05, Vol.96 (2), p.266-274

58.
Converging Mechanisms in ALS and FTD: Disrupted RNA and Protein Homeostasis
by Ling, Shuo-Chien
Neuron (Cambridge, Mass.), 2013-08-07, Vol.79 (3), p.416-438

59.
Mutations in PIEZO2 Cause Gordon Syndrome, Marden-Walker Syndrome, and Distal Arthrogryposis Type 5
by McMillin, Margaret J
American journal of human genetics, 2014-05-01, Vol.94 (5), p.734-744

60.
Dimeric CRISPR RNA-guided FokI nucleases for highly specific genome editing
by Tsai, Shengdar Q
Nature biotechnology, 2014-06, Vol.32 (6), p.569-576
