Magnus Nordenskj�ld
Karolinska University Hospital(SE)Karolinska Institutet(SE)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Prenatal Screening and Diagnostics, Genetic factors in colorectal cancer, DNA Repair Mechanisms, Neuroendocrine Tumor Research Advances
Most-Cited Works
- → Mutation in the DNA mismatch repair gene homologue hMLH 1 is associated with hereditary non-polyposis colon cancer(1994)2,065 cited
- → Highly abnormal cleavage divisions in preimplantation embryos from translocation carriers(2000)111 cited
- → Analysis of short stature homeobox-containing gene ( SHOX ) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity(2001)60 cited
- → Distinct deleted regions on chromosome segment 16q23-24 associated with metastases in prostate cancer(1999)55 cited
- → Isolation and mapping of polymorphic cosmid clones used for sublocalization of the multiple endocrine neoplasia type 1 (MEN1) locus(1992)42 cited
- → Four separate regions on chromosome 17 show loss of heterozygosity in familial breast carcinomas(1993)31 cited
- → Molecular analysis of 4p deletion associated with Wolf-Hirschhorn syndrome moving the ?critical segment? towards the telomere(1991)28 cited
- → Early prenatal diagnosis of the ICF syndrome(2000)19 cited
- → A normal male with an inherited deletion of one exon within the DMD gene(1990)16 cited
- → Sublocalization of a locus at 3p21.3?23 predisposing to hereditary nonpolyposis colon cancer(1994)13 cited