Hultén, Maj A.. (2011) On the origin of crossover interference : a chromosome oscillatory movement (COM) model. Molecular Cytogenetics, Vol.4 (No.10). ISSN 1755-8166

Della Ragione, Floriana, Mastrovito, Paola, Campanile, Ciro, Conti, Anna, Papageorgiou, Elisavet A., Hultén, Maj A., Patsalis, Philippos C., Carter, Nigel P. and D'Esposito, Maurizio. (2010) Differential DNA methylation as a tool for noninvasive prenatal diagnosis (NIPD) of X chromosome aneuploidies. The Journal of Molecular Diagnostics, Vol.12 (No.6). pp. 797-807. ISSN 1525-1578

Hultén, Maj A., Jonasson, Jon, Nordgren, Ann and Iwarsson, Erik. (2010) Germinal and somatic trisomy 21 mosaicism : how common is it, what are the implications for individual carriers and how does it come about? Current Genomics, Vol.11 (No.6). pp. 409-419. ISSN 1389-2029

Hultén, Maj A., Patel, Suketu D., Westgren, Magnus, Papadogiannakis, Nikos, Jonsson, Anna Maria, Jonasson, Jon and Iwarsson, Erik. (2010) On the paternal origin of trisomy 21 Down syndrome. Molecular Cytogenetics, Vol.3 (No.1). p. 4. ISSN 1755-8166

Hultén, Maj A., Patel, Suketu, Jonasson, Jon and Iwarsson, Erik (2010) On the origin of the maternal age effect in trisomy 21 Down syndrome : the Oocyte Mosaicism Selection model. Reproduction, Vol.139 (No.1). pp. 1-9. ISSN 1470-1626

Hultén, Maj A. (2009) Non-invasive prenatal diagnosis: another new concept in need of a definition. Reproductive Biomedicine Online, Vol.19 (No.5). p. 756. ISSN 1472-6483

Hu, Suwei, Zhong, Yanfang, Hao, Yuantao, Luo, Minqi, Zhou, Yan, Guo, Hui, Liao, Weijiao, Wan, Desheng, Wei, Haiyun, Gao, Yueting, Shan, Jinglan, Hu, Bin, Hultén, Maj A. and Wang, Yiming. (2009) Novel rare alleles of ABCA1 are exclusively associated with extreme high-density lipoprotein-cholesterol levels among the Han Chinese. Clinical Chemistry and Laboratory Medicine, Vol.47 (No.10). pp. 1239-1245. ISSN 1434-6621

Middlemiss, Prisca, Wynn, S. L. and Hultén, Maj A. (2009) Development of a set of family-friendly leaflets on rare chromosome disorders for use by families and professionals. In: British Human Genetics Conference, University of Warwick, England, AUG 31-SEP 02, 2009. Published in: Journal of Medical Genetics, Vol.46 (Suppl. 1). S106-S106.

Stergianou, K., Carpenter, K., Ocraft, K., Cross, G., Hultén, Maj A. and Parkin, T. (2009) Evaluation of technologies for detection and quantification of foetal DNA in maternal plasma in a clinical setting. In: British Human Genetics Conference, University of Warwick, England, September 23-25, 2002. Published in: Journal of Medical Genetics, Vol.46 (Suppl. 1). S28-S28.

Hultén, Maj A. (2009) Introduction to session "Trisomy 21 Down Syndrome, fifty years on: where are we now?". In: British Human Genetics Conference, University of Warwick, England, AUG 31-SEP 02, 2009. Published in: Journal of Medical Genetics, Vol.46 (Suppl. 1). S21-S21.

Hultén, Maj A. and Patel, S. (2009) On the origin of constitutional aneuploidy: ovarian aneuploidy mosaicism. In: British Human Genetics Conference, University of Warwick, England, August 31-SEP 02, 2009. Published in: Journal of Medical Genetics, Vol.46 (Suppl. 1). S97-S97.

Hultén, Maj A. and Iwarsson, Erik (2009) On the origin of trisomy 21-the evidence from oocyte and polar body analysis. In: British Human Genetics Conference, University of Warwick, England, AUG 31-SEP 02, 2009. Published in: Journal of Medical Genetics, Vol.46 (Suppl. 1). S97-S97.

Moffat, Kevin G., Patel, S. and Hultén, Maj A. (2009) Trisomy21, Down Syndrome and the origin of Alzheimer's disease. In: British Human Genetics Conference, University of Warwick, England, AUG 31-SEP 02, 2009. Published in: Journal of Medical Genetics, Vol.46 (Suppl. 1). S22-S22.

Stergianou, K., Carpenter, K., Ocraft, K., Cross, G., Hultén, Maj A. and Parkin, T. (2009) Evaluation of technologies for detection and quantification of foetal DNA in maternal plasma in a clinical setting. In: 7th European Cytogenetics Conference, Stockholm, Sweden, Jul 04-07, 2009. Published in: Chromosome Research, Vol.17 (Suppl. 1). p. 221.

Hultén, Maj A. (2009) Inborn aneuploidy: how does it come about? The maternal side. In: 7th European Cytogenetics Conference, Stockholm, Sweden, July 04-07, 2009. Published in: Chromosome Research, Vol.17 (Suppl. 1). p. 17.

Hultén, Maj A. and Iwarsson, Erik (2009) On the origin of constitutional aneuploidy. In: 7th European Cytogenetics Conference, Stockholm, Sweden, July 04-07, 2009. Published in: Chromosome Research, Vol.17 (Suppl. 1). pp. 108-109.

Papageorgiou, Elisavet A., Fiegler, Heike, Rakyan, Vardhman, Beck, Stephan, Hultén, Maj A., Lamnissou, Klea, Carter, Nigel P. and Patsalis, Philippos C.. (2009) Sites of differential DNA methylation between placenta and peripheral blood molecular markers for noninvasive prenatal diagnosis of aneuploidies. American Journal of Pathology, Vol.174 (No.5). pp. 1609-1618. ISSN 0002-9440

Hultén, Maj A., Patel, Suketu D., Tankimanova, Maira, Westgren, Magnus, Papadogiannakis, Nikos, Jonsson, Anna Maria and Iwarsson, Erik. (2008) On the origin of trisomy 21 Down syndrome. Molecular Cytogenetics, Vol.1 (No.21). ISSN 1755-8166

Hultén, Maj A. (2008) On the origin of Down syndrome. In: British Human Genetics Conference, Univ York, York, England, Sep 15-17, 2008. Published in: Journal of Medical Genetics, Vol.45 (Suppl.1). S32-S32.

. (2008) Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome). Journal of Medical Genetics, Vol.45 (No.2). pp. 93-99. ISSN 0022-2593

Legler, Tobias J., Liu, Zhong, Mavrou, Ariadni, Finning, Kirstin, Hromadnikova, Ilona, Galbiati, Silvia, Meaney, Cathy, Hultén, Maj A., Crea, Francesco , Olsson, Martin L., Maddocks, Deborah G., Huang, Dorothy, Fisher, Sylvia Armstrong, Sprenger-Haussels, Markus, Soussan, Aicha Ait and van der Schoot, C. Ellen. (2007) Workshop report on the extraction of foetal DNA from maternal plasma. Prenatal Diagnosis, Vol.27 (No.9). pp. 824-829. ISSN 0197-3851

Old, Robert W. , Crea, Francesco, Puszyk, William Matthew and Hultén, Maj A.. (2007) Candidate epigenetic biomarkers for non-invasive prenatal diagnosis of Down syndrome. Reproductive Biomedicine Online, Vol.15 (No.2). pp. 227-235. ISSN 1472-6483

Hultén, Maj A. and Old, Robert W. (2007) Non-invasive prenatal diagnosis of Down's syndrome. Lancet, Vol.369 (No.9578). p. 1997. ISSN 0140-6736

Hultén, Maj A., Crea, F., Puszyk, W. M. and Old, R. W. (2007) Towards noninvasive prenatal diagnosis of trisomy 21 Down syndrome. In: 6th European Cytogenetics Conference, Istanbul, TURKEY, JUL 07-10, 2007. Published in: CHROMOSOME RESEARCH, 15 (Suppl. 1). pp. 242-243.

Knudsen, Gun Peggy S., Neilson, Tracey C. S., Pedersen, June, Kerr, Alison, Schwartz, Marianne, Hultén, Maj A., Bailey, Mark E. S. and Orstavik, Karen Helene. (2006) Increased skewing of X chromosome inactivation in Rett syndrome patients and their mothers. EUROPEAN JOURNAL OF HUMAN GENETICS, 14 (11). pp. 1189-1194. ISSN 1018-4813

Hultén, Maj A.. (2006) Altered patterns of meiotic recombination in human fetal oocytes with asynapsis and/or synaptonemal complex fragmentation at pachytene. REPRODUCTIVE BIOMEDICINE ONLINE, 13 (1). pp. 88-95. ISSN 1472-6483

Tease, C. and Hultén, Maj A.. (2004) Inter-sex variation in synaptonemal complex lengths largely determine the different recombination rates in male and female germ cells. Cytogenetic and Genome Research, Vol.107 (No.3-4). pp. 208-215. ISSN 1424-8581

Grimshaw, G. M., Szczepura, Ala, Hultén, Maj A., MacDonald, F. and Nevin, N. C. (2003) Evaluation of molecular tests for prenatal diagnosis of chromosome abnormalities. Health Technology Assessment, Vol.7 (No.10). ISSN 1366-5278

Lyrakou, S., Hultén, Maj A. and Hartshorne, Geraldine M.. (2002) Growth factors promote meiosis in mouse fetal ovaries in vitro. Molecular Human Reproduction, Vol.8 (No.10). pp. 906-911. ISSN 1360-9947