Author

Herdis Steingrimsdottir

Observed names: H Steingrimsdottir, H. STEINGRIMSDOTTIR, H. Steingrimsdottir, Herdís Steingrímsdóttir, Steingrimsdottir, H, Steingrimsdottir, Herdis, Steingrímsdóttir, Herdís

Institution: Copenhagen Business School

Observed institutions: University of Hawaiʻi at Mānoa, University of Copenhagen, National Bureau of Economic Research, Karolinska University Hospital, University of Sussex, Copenhagen Business School, King's College London, IZA - Institute of Labor Economics, Princess Anne Hospital, University of California San Diego, National University Hospital of Iceland, King's College School, Centre international de recherche sur le cancer, University of Southampton, Medical Research Council

ORCID: 0000-0002-0189-5980

Observed ORCID: 0000-0002-0189-5980

OpenAlex ID: A5037430044

Molecular and Biochemical Characterization of xrs Mutants Defective in Ku80

1997 · B. K. Singleton, A. Priestley, et al. · Molecular and Cellular Biology · 183

Molecular Analysis of Mutations in the CSB(ERCC6) Gene in Patients with Cockayne Syndrome

1998 · Donna L. Mallery, Bianca Tanganelli, et al. · The American Journal of Human Genetics · 163

Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy

1994 · Bernard C. Broughton, Herdis Steingrimsdottir, et al. · Nature Genetics · 132

Mutations which alter splicing in the human hypoxanthine-guanine phosphoribosyltransferase gene

1992 · H. Steingrimsdottir, G. Rowley, et al. · Nucleic Acids Research · 130

Trichothiodystrophy, a human DNA repair disorder with heterogeneity in the cellular response to ultraviolet light.

1988 · A R Lehmann, C F Arlett, et al. · PubMed · 105

The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms

2014 · A Oddsson, S Y Kristinsson, et al. · Leukemia · 95

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Role of p16/MTS1, cyclin D1 and RB in primary oral cancer and oral cancer cell lines

1999 · M Sartor, H Steingrimsdottir, et al. · British Journal of Cancer · 92

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Mutant sequences in the rpsL gene of Escherichia coli B/r: Mechanistic implications for spontaneous and ultraviolet light mutagenesis

1992 · A.R. Timms, H. Steingrimsdottir, et al. · Molecular and General Genetics MGG · 92

Immune reconstitution after autologous hematopoietic stem cell transplantation in relation to underlying disease, type of high-dose therapy and infectious complications.

2000 · H Steingrimsdottir, A Gruber, et al. · PubMed · 80

Prevalence of human papillomavirus infection in premalignant and malignant lesions of the oral cavity in U.K. subjects: a novel method of detection

1998 · F Elamin, H Steingrimsdottir, et al. · Oral Oncology · 64

Relation between the human fibroblast strain 46BR and cell lines representative of Bloom's syndrome.

1988 · A R Lehmann, A E Willis, et al. · PubMed · 61

Five polymorphisms in the coding sequence of the xeroderma pigmentosum group D gene

1996 · Bernard C Broughton, Herdis Steingrimsdottir, et al. · Mutation Research/DNA Repair · 60

Molecular analysis of ultraviolet-induced mutations in a xeroderma pigmentosum cell line

1991 · G. Dorado, H. Steingrimsdottir, et al. · Journal of Molecular Biology · 59

How Does Daddy at Home Affect Marital Stability?

2020 · Arna Olafsson, Herdis Steingrimsdottir · The Economic Journal · 58

Inactivation of a Transfected Gene in Human Fibroblasts Can Occur by Deletion, Amplification, Phenotypic Switching, or Methylation

1987 · M M Gebara, C Drevon, et al. · Molecular and Cellular Biology · 52

Loss of heterozygosity on chromosome 5q in ovarian cancer is frequently accompanied by TP53 mutation and identifies a tumour suppressor gene locus at 5q13.1-21

1996 · M Tavassoli, H Steingrimsdottir, et al. · British Journal of Cancer · 51

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Molecular analysis of mutations in the hprt gene in circulating lymphocytes from normal and DNA-repair-deficient donors

1993 · H. Steingrimsdottir, G. Rowley, et al. · Mutation Research/DNA Repair · 48

SV40-transformed normal and DNA-repair-deficient human fibroblasts can be transfected with high frequency but retain only limited amounts of integrated DNA

1988 · Lynne V. Mayne, Tina Jones, et al. · Gene · 48

p53 aberrations in oral submucous fibrosis and oral squamous cell carcinoma detected by immunocytochemistry and PCR‐SSCP

1998 · C. Trivedy, K. A. A. S. Warnakulasuriya, et al. · Journal of Oral Pathology and Medicine · 42

HPRT somatic mutation data.

1990 · J Cole, M H Green, et al. · PubMed · 27

Reproductive rights and the career plans of U.S. college freshmen

2016 · Herdis Steingrimsdottir · Labour Economics · 21

1997 · Yafei Liu, Gino Cortopassi, et al. · Environmental and Molecular Mutagenesis · 19

Improved progression free survival with bortezomib consolidation after high dose melphalan: results of a randomised phase III trial

2011 · Mellquist, U. H., Gimsing, P, et al. · University of Southern Denmark Research Portal (University of Southern Denmark) · 18

The Long-term Impact of Children's Disabilities on Families

2019 · Snaebjorn Gunnsteinsson, Herdis Steingrimsdottir · RePEc: Research Papers in Economics · 17

p53 alterations and HPV infections are common in oral SCC: p53 gene mutations correlate with the absence of HPV 16-E6 DNA.

1998 · J Penhallow, H Steingrimsdottir, et al. · International Journal of Oncology · 17

Works count: 60

Citation count: 1,891

H-index: 21

I10-index: 31