Cracking the genome: Inside the race to unlock human DNA K Davies JHU Press, 2002 | 242 | 2002 |
The $1,000 genome: the revolution in DNA sequencing and the new era of personalized medicine K Davies Simon and Schuster, 2015 | 142 | 2015 |
Chromosome 7 long arm deletion in myeloid disorders: a narrow breakpoint region in 7q22 defined by molecular mapping J Kere, T Ruutu, KA Davies, IB Roninson, PC Watkins, R Winqvist, ... | 90 | 1989 |
Breakthrough: the race to find the breast cancer gene K Davies, M White | 69 | 1996 |
Hereditary disorders of the red cell membrane skeleton KA Davies, SE Lux Trends in Genetics 5, 222-227, 1989 | 58 | 1989 |
The essence of inactivity K Davies Nature 349 (6304), 15-16, 1991 | 45 | 1991 |
DNA: The Story of the Genetic Revolution JD Watson, A Berry, K Davies Knopf, 2017 | 40 | 2017 |
Closing the Menkes disease gene. K Davies Nature 361 (6407), 1993 | 37 | 1993 |
The sequence: Inside the race for the human genome K Davies Phoenix, 2002 | 31 | 2002 |
Cystic fibrosis. Complementary endeavours. K Davies Nature 348 (6297), 110-111, 1990 | 29 | 1990 |
Reactions to the National Academies/Royal Society Report on Heritable Human Genome Editing M Angrist, R Barrangou, F Baylis, C Brokowski, G Burgio, A Caplan, ... The CRISPR journal 3 (5), 332-349, 2020 | 28 | 2020 |
Editing humanity: The CRISPR revolution and the new era of genome editing K Davies Simon and Schuster, 2020 | 24 | 2020 |
Cystic fibrosis carrier detection using a linked gene probe. M Farrall, P Scambler, KW Klinger, K Davies, C Worrall, R Williamson, ... Journal of medical genetics 23 (4), 295-299, 1986 | 22 | 1986 |
After the genome: DNA and human disease K Davies Cell 104 (4), 465-467, 2001 | 19 | 2001 |
Breaking the fragile X K Davies Nature 351 (6326), 439-440, 1991 | 16 | 1991 |
Deficiency of band-3 in dominant hereditary spherocytosis with normal spectrin content S Lux, C Bedrosian, O Shalev, M Morris, J Chasis, K Davies, P Savvides, ... Clinical Research 38 (2), A300-A300, 1990 | 16 | 1990 |
Further data supporting linkage between cystic fibrosis and the met oncogene and haplotype analysis with met and pJ3. 11 M Farrall, E Watson, G Bates, G Bell, J Bell, KA Davies, X Estivill, H Kruyer, ... American journal of human genetics 39 (6), 713, 1986 | 16 | 1986 |
The $1,000,000 Genome Interpretation K Davies Australian Life Scientist 8 (1), 50-54, 2011 | 15 | 2011 |
Who's on Third? K DAVIES Bio-IT World 9 (5), 2010 | 15* | 2010 |
Complementary endeavours K Davies Nature 348 (6297), 110-111, 1990 | 15 | 1990 |