| Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene GL Xu, TH Bestor, D Bourc'his, CL Hsieh, N Tommerup, M Bugge, ... Nature 402 (6758), 187-191, 1999 | 1446 | 1999 |
| Chiasma distribution at diakinesis in the normal human male MAJ Hultén Hereditas 76 (1), 55-78, 1974 | 357 | 1974 |
| Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location JP Cheadle, H Gill, N Fleming, J Maynard, A Kerr, H Leonard, ... Human molecular genetics 9 (7), 1119-1129, 2000 | 330 | 2000 |
| Crossing over analysis at pachytene in man AL Barlow, MA Hulten European Journal of Human Genetics 6 (4), 350-358, 1998 | 225 | 1998 |
| Rapid and simple prenatal diagnosis of common chromosome disorders: advantages and disadvantages of the molecular methods FISH and QF-PCR MA Hulten, S Dhanjal, B Pertl REPRODUCTION-CAMBRIDGE- 126 (3), 279-297, 2003 | 222 | 2003 |
| Distribution of the Rad51 recombinase in human and mouse spermatocytes AL Barlow, FE Benson, SC West, MA Hultén The EMBO journal, 1997 | 211 | 1997 |
| Rapid and simple prenatal DNA diagnosis of Down's syndrome L Verma, F Macdonald, P Leedham, M McConachie, S Dhanjal, M Hulten The Lancet 352 (9121), 9-12, 1998 | 209 | 1998 |
| Further studies on bivalent chiasma frequency in human males with normal karyotypes DA Laurie, MA Hultén Annals of human genetics 49 (3), 189-201, 1985 | 191 | 1985 |
| Patterns of meiotic recombination in human fetal oocytes C Tease, GM Hartshorne, MA Hultén The American Journal of Human Genetics 70 (6), 1469-1479, 2002 | 181 | 2002 |
| Nuclear weapons tests and human germline mutation rate YE Dubrova, RI Bersimbaev, LB Djansugurova, MK Tankimanova, ... Science 295 (5557), 1037-1037, 2002 | 179 | 2002 |
| Guidelines for reporting clinical features in cases with MECP2 mutations AM Kerr, Y Nomura, D Armstrong, M Anvret, PV Belichenko, S Budden, ... Brain and Development 23 (4), 208-211, 2001 | 178 | 2001 |
| Sites of differential DNA methylation between placenta and peripheral blood: molecular markers for noninvasive prenatal diagnosis of aneuploidies EA Papageorgiou, H Fiegler, V Rakyan, S Beck, M Hulten, K Lamnissou, ... The American journal of pathology 174 (5), 1609-1618, 2009 | 175 | 2009 |
| Childhood cancer and parental use of tobacco: deaths from 1971 to 1976 T Sorahan, P Prior, RJ Lancashire, SP Faux, MA Hulten, IM Peck, ... British journal of cancer 76 (11), 1525-1531, 1997 | 171 | 1997 |
| Quantification of human seminiferous epithelium NE Skakkebaek, MAJ HULTÉN, P JACOBSEN, M MIKKELSEN Reproduction 32 (3), 391-401, 1973 | 164 | 1973 |
| Inter-sex variation in synaptonemal complex lengths largely determine the different recombination rates in male and female germ cells C Tease, MA Hultén Cytogenetic and genome research 107 (3-4), 208-215, 2004 | 158 | 2004 |
| Mammalian meiotic telomeres: protein composition and redistribution in relation to nuclear pores H Scherthan, M Jerratsch, B Li, S Smith, M Hultén, T Lock, T de Lange Molecular biology of the cell 11 (12), 4189-4203, 2000 | 156 | 2000 |
| Candidate epigenetic biomarkers for non-invasive prenatal diagnosis of Down syndrome RW Old, F Crea, W Puszyk, MA Hultén Reproductive biomedicine online 15 (2), 227-235, 2007 | 155 | 2007 |
| On the origin of trisomy 21 Down syndrome MA Hultén, SD Patel, M Tankimanova, M Westgren, N Papadogiannakis, ... Molecular Cytogenetics 1, 1-10, 2008 | 151 | 2008 |
| Childhood cancer and parental use of tobacco: deaths from 1953 to 1955 T Sorahan, RJ Lancashire, MA Hulten, I Peck, AM Stewart British Journal of Cancer 75 (1), 134-138, 1997 | 151 | 1997 |
| Genotype-phenotype correlation between position of constitutional APC gene mutation and CHRPE expression in familial adenomatous polyposis YL Wallis, F Macdonald, M Hultén, JEV Morton, CM McKeown, ... Human genetics 94, 543-548, 1994 | 141 | 1994 |
