| Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresis S Kenwrick, M Patterson, A Speer, K Fischbeck, K Davies Cell 48 (2), 351-357, 1987 | 202 | 1987 |
| Disorder-induced coherent scattering in slow-light photonic crystal waveguides M Patterson, S Hughes, S Combrié, NVQ Tran, A De Rossi, R Gabet, ... Physical review letters 102 (25), 253903, 2009 | 177 | 2009 |
| Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity syndrome JA Batch, DM Williams, HR Davies, BD Brown, BAJ Evans, IA Hughes, ... Human molecular genetics 1 (7), 497-503, 1992 | 176 | 1992 |
| Molecular Characterization of Cell Cycle Gene CDC7 from Saccharomyces cerevisiae M Patterson, RA Sclafani, WL Fangman, J Rosamond Molecular and cellular biology 6 (5), 1590-1598, 1986 | 170 | 1986 |
| Ultrahigh Purcell factors and Lamb shifts in slow-light metamaterial waveguides P Yao, C Van Vlack, A Reza, M Patterson, MM Dignam, S Hughes Physical Review B—Condensed Matter and Materials Physics 80 (19), 195106, 2009 | 140 | 2009 |
| Chromosome-specific alpha satellite DNA from human chromosome 1: hierarchical structure and genomic organization of a polymorphic domain spanning several hundred kilobase pairs … JS Waye, SJ Durfy, D Pinkel, S Kenwrick, M Patterson, KE Davies, ... Genomics 1 (1), 43-51, 1987 | 119 | 1987 |
| Differential regulation of the yeast CDC7 gene during mitosis and meiosis RA Sclafani, M Patterson, J Rosamond, WL Fangman Molecular and cellular biology, 1988 | 111 | 1988 |
| Androgen insensitivity syndrome: a survey of diagnostic procedures and management in the UK RM Viner, Y Teoh, DM Williams, MN Patterson, IA Hughes Archives of Disease in Childhood 77 (4), 305-309, 1997 | 101 | 1997 |
| Disorder-induced incoherent scattering losses in photonic crystal waveguides: Bloch mode reshaping, multiple scattering, and breakdown of the Beer-Lambert law M Patterson, S Hughes, S Schulz, DM Beggs, TP White, L O’Faolain, ... Physical Review B—Condensed Matter and Materials Physics 80 (19), 195305, 2009 | 97 | 2009 |
| Functional analysis of six androgen receptor mutations identified in patients with partial androgen insensitivity syndrome CL Bevan, BB Brown, HR Davies, BAJ Evans, IA Hughes, MN Patterson Human Molecular Genetics 5 (2), 265-273, 1996 | 90 | 1996 |
| Evidence that xeroderma pigmentosum cells from complementation group E are deficient in a homolog of yeast photolyase M Patterson, G Chu Molecular and cellular biology 9 (11), 5105-5112, 1989 | 77 | 1989 |
| Phenotypic diversity in siblings with partial androgen insensitivity syndrome BAJ Evans, IA Hughes, CL Bevan, MN Patterson, JW Gregory Archives of disease in childhood 76 (6), 529-531, 1997 | 76 | 1997 |
| MASA syndrome: further clinical delineation and chromosomal localisation RM Winter, KE Davies, MV Bell, SM Huson, MN Patterson Human genetics 82, 367-370, 1989 | 73 | 1989 |
| 8 Androgen insensitivity syndrome MN Patterson, MJ McPhaul, IA Hughes Baillière's clinical endocrinology and metabolism 8 (2), 379-404, 1994 | 71 | 1994 |
| Physical mapping studies on the human X chromosome in the region Xq27-Xqter M Patterson, C Schwartz, M Bell, S Sauer, M Hofker, B Trask, ... Genomics 1 (4), 297-306, 1987 | 68 | 1987 |
| Mutational screening of the Wilms's tumour gene, WT1, in males with genital abnormalities. PA Clarkson, HR Davies, DM Williams, R Chaudhary, IA Hughes, ... Journal of medical genetics 30 (9), 767-772, 1993 | 66 | 1993 |
| Mapping of DNA markers close to the fraglle site on the human X chromosome at Xq25–3 M Patterson, S Kenwrick, S Thibodeau, K Faulk, MG Mattei, JF Mattei, ... Nucleic acids research 15 (6), 2639-2651, 1987 | 60 | 1987 |
| Mutations of the androgen receptor gene identified in perineal hypospadias. JA Batch, BA Evans, IA Hughes, MN Patterson Journal of medical genetics 30 (3), 198-201, 1993 | 52 | 1993 |
| Phenotypic variation and detection of carrier status in the partial androgen insensitivity syndrome. JA Batch, HR Davies, BA Evans, IA Hughes, MN Patterson Archives of disease in childhood 68 (4), 453-457, 1993 | 51 | 1993 |
| Physical linkage of a GABAA receptor subunit gene to the DXS374 locus in human Xq28. MV Bell, J Bloomfield, M McKinley, MN Patterson, MG Darlison, ... American journal of human genetics 45 (6), 883, 1989 | 50 | 1989 |
