Maj Hultén - Concepedia

Author

Maj Hultén

University of Warwick ORCID

Also Known As

M A Hulten, M A Hultén, M Hulten, M Hultén, M. A. HULTÉN, M. A. Hulten, M. A. Hultén, M. HULTÉN, M. Hulten, M. Hultén

225

Publications

Citations

H-Index

132

Concepts

All Affiliations

University of Warwick Karolinska University Hospital Heartlands Hospital Karolinska Institutet University of Birmingham

About

Maj Hultén is an author at University of Warwick specializing in medicine, genetics, and cytogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	35	68	4.9K
2	Public Health	18	26	1.2K
3	Natural Sciences	8	8	1.7K
4	Health Sciences	5	5	242
5	Engineering	2	2	180

Maj Hultén

118

Publications

7.4K

Citations

H-Index

Page 1

	Year	Citations
Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene Guoliang Xu, Timothy H. Bestor, Déborah Bourc’his, Nature ChromatinGenome InstabilityChromosome InstabilityGenetic DisorderNatural Sciences	1999	1.2K
Chiasma distribution at diakinesis in the normal human male Maj Hultén Hereditas CytogeneticsGeneticsPathologyDermatologyPathologic Lesion	2009	291
Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome) Melanie M. Hagleitner, Arjan C. Lankester, P Maraschio, Journal of Medical Genetics	2007	215
Further studies on bivalent chiasma frequency in human males with normal karyotypes D. A. Laurie, Maj Hultén Annals of Human Genetics SpermatogenesisCytogeneticsTriple Staining TechniqueGeneticsHuman Males	1985	157
Mammalian Meiotic Telomeres: Protein Composition and Redistribution in Relation to Nuclear Pores Harry Scherthan, Martin Jerratsch, Bibo Li, Molecular Biology of the Cell Protein CompositionGeneticsMolecular BiologyReproductive BiologySomatic Telomeres	2000	154
Patterns of Meiotic Recombination in Human Fetal Oocytes C. Tease, Geraldine Hartshorne, Maj Hultén The American Journal of Human Genetics OocyteInfertilityDevelopmental BiologyFertilityCell Division	2002	153
Guidelines for reporting clinical features in cases with MECP2 mutations Alison Kerr, Yoshiko Nomura, Dawna Armstrong, Brain and Development Genetic DisorderGeneticsMecp2 MutationsPathologyMedical Genetics	2001	146
Nuclear Weapons Tests and Human Germline Mutation Rate Yuri E. Dubrova, Rakhmet I. Bersimbaev, Leyla Djansugurova, Science Genetic TestingEngineeringSoviet UnionMutation-based TestingMedicine	2002	142
On the origin of trisomy 21 Down syndrome Maj Hultén, Suketu D Patel, Maira Tankimanova, Molecular Cytogenetics	2008	139
Rapid and simple prenatal DNA diagnosis of Down's syndrome Louisa Verma, Fiona MacDonald, P W Leedham, The Lancet Down SyndromePrenatal Genetic TestingGenetic DisorderGeneticsDiagnosis	1998	137

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