| Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17 D Barker, K Wright, K Nguyen, I Cannon, P Fain, D Goldgar, DT Bishop, ... Science 236 (May 29), 1100-1102, 1987 | 919 | 1987 |
| Improved DNA extraction from ancient bones using silica‐based spin columns DY Yang, B Eng, JS Waye, JC Dudar, SR Saunders American Journal of Physical Anthropology: The Official Publication of the …, 1998 | 812 | 1998 |
| Hierarchical order in chromosome-specific human alpha satellite DNA HF Willard, JS Waye Trends in Genetics 3, 192-198, 1987 | 659 | 1987 |
| Fixed-bin analysis for statistical evaluation of continuous distributions of allelic data from VNTR loci, for use in forensic comparisons. B Budowle, AM Giusti, JS Waye, FS Baechtel, RM Fourney, DE Adams, ... American Journal of Human Genetics 48 (5), 841, 1991 | 325 | 1991 |
| Hydrops fetalis caused by α-thalassemia: an emerging health care problem DHK Chui, JS Waye Blood, The Journal of the American Society of Hematology 91 (7), 2213-2222, 1998 | 305 | 1998 |
| Structure, organization, and sequence of alpha satellite DNA from human chromosome 17: evidence for evolution by unequal crossing-over and an ancestral pentamer repeat shared … JS Waye, HF Willard Molecular and cellular biology 6 (9), 3156-3165, 1986 | 305 | 1986 |
| Prevalence and genotypes of α-and β-thalassemia carriers in Hong Kong—implications for population screening YL Lau, LC Chan, YYA Chan, SY Ha, CY Yeung, JS Waye, DHK Chui New England journal of medicine 336 (18), 1298-1301, 1997 | 290 | 1997 |
| Genomic organization of alpha satellite DNA on human chromosome 7: evidence for two distinct alphoid domains on a single chromosome JS Waye, SB England, HF Willard Molecular and cellular biology 7 (1), 349-356, 1987 | 257 | 1987 |
| A simple and sensitive method for quantifying human genomic DNA in forensic specimen extracts. JS Waye, LA Presley, B Budowle, GG Shutler, RM Fourney Biotechniques 7 (8), 852-855, 1989 | 251 | 1989 |
| Nucleotide sequence heterogeneity of alpha satellite repetitive DNA: a survey of alphoid sequences from different human chromosomes JS Waye, HF Willard Nucleic acids research 15 (18), 7549-7569, 1987 | 247 | 1987 |
| Chromosome-specific alpha satellite DNA: nucleotide sequence analysis of the 2.0 kilobasepair repeat from the human X chromosome JS Waye, HF Willard Nucleic acids research 13 (8), 2731-2743, 1985 | 241 | 1985 |
| Chromosome-specific subsets of human alpha satellite DNA: analysis of sequence divergence within and between chromosomal subsets and evidence for an ancestral pentameric repeat HF Willard, JS Waye Journal of molecular evolution 25, 207-214, 1987 | 209 | 1987 |
| Human beta satellite DNA: genomic organization and sequence definition of a class of highly repetitive tandem DNA. JS Waye, HF Willard Proceedings of the National Academy of Sciences 86 (16), 6250-6254, 1989 | 195 | 1989 |
| Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach B Giardine, J Borg, DR Higgs, KR Peterson, S Philipsen, D Maglott, ... Nature genetics 43 (4), 295-301, 2011 | 179 | 2011 |
| Changes in the epidemiology of thalassemia in North America: a new minority disease EP Vichinsky, EA MacKlin, JS Waye, F Lorey, NF Olivieri Pediatrics 116 (6), e818-e825, 2005 | 174 | 2005 |
| Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for … HF Willard, JS Waye, MH Skolnick, CE Schwartz, VE Powers, SB England Proceedings of the National Academy of Sciences 83 (15), 5611-5615, 1986 | 164 | 1986 |
| Molecular analysis of a deletion polymorphism in alpha satellite of human chromosome 17: evidence for homologous unequal crossing-over and subsequent fixation JS Waye, HF Willard Nucleic acids research 14 (17), 6915-6927, 1986 | 130 | 1986 |
| 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 | 118 | 1987 |
| Hb H hydrops foetalis syndrome: a case report and review of literature F Lorey, P Charoenkwan, HE Witkowska, J Lafferty, M Patterson, B Eng, ... British journal of haematology 115 (1), 72-78, 2001 | 113 | 2001 |
| Universal newborn screening for Hb H disease in California F Lorey, G Cunningham, EP Vichinsky, BH Lubin, HE Witkowska, ... Genetic testing 5 (2), 93-100, 2001 | 113 | 2001 |
