Charlotte Brasch-Andersen

Clinical Laboratory Geneticist (ErCLG), MSc, PhD

  • Campusvej 55

    5230 Odense M

    Denmark

20022020

Research output per year

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Research Output

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Journal article
2020

A new 1p36.13-1p36.12 microdeletion syndrome characterized by learning disability, behavioral abnormalities, and ptosis

Aagaard Nolting, L., Brasch-Andersen, C., Cox, H., Kanani, F., Parker, M., Fry, A. E., Loddo, S., Novelli, A., Dentici, M. L., Joss, S., Jørgensen, J. P. & Fagerberg, C. R., Jun 2020, In : Clinical Genetics. 97, 6, p. 927-932

Research output: Contribution to journalJournal articleResearchpeer-review

Heme oxygenase 1 polymorphism, occupational vapor, gas, dust, and fume exposure and chronic obstructive pulmonary disease in a Danish population-based study

Würtz, E. T., Brasch-Andersen, C., Steffensen, R., Hansen, J. G., Malling, T. H., Schlünssen, V. & Omland, Ø., 1. Jan 2020, In : Scandinavian Journal of Work, Environment & Health. 46, 1, p. 96-104

Research output: Contribution to journalJournal articleResearchpeer-review

Open Access
2019

CD18 is redundant for the response to multiple vaccines: A case study

Assing, K., Nielsen, C., Hansen, H. T., Jakobsen, M. A., Skogstrand, K., Brasch- Andersen, C., Hartling, U. B. & Fisker, N., Feb 2019, In : Pediatric Allergy and Immunology. 30, 1, p. 136-139

Research output: Contribution to journalJournal articleResearchpeer-review

Open Access
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48 Downloads (Pure)

Endometrioidt adenokarcinom med samtidigt nongestationelt koriokarcinom i uterus

Translated title of the contribution: Endometrioid adenocarcinoma with a co-existing non-gestational choriocarcinoma in uterusNeumann, G., Brasch-Andersen, C., Fagerberg, C. & Schledermann, D., 18. Nov 2019, In : Ugeskrift for Laeger. 181, V03190167.

Research output: Contribution to journalJournal articleResearchpeer-review

Enriched power of disease-concordant twin-case-only design in detecting interactions in genome-wide association studies

Li, W., Baumbach, J., Mohammadnejad, A., Brasch-Andersen, C., Vandin, F., Korbel, J. O. & Tan, Q., 1. Apr 2019, In : European Journal of Human Genetics. 27, 4, p. 631-636

Research output: Contribution to journalJournal articleResearchpeer-review

Open Access
File
75 Downloads (Pure)

Estimating the effect size of the 15Q11.2 BP1-BP2 deletion and its contribution to neurodevelopmental symptoms: recommendations for practice

Jønch, A. E., Douard, E., Moreau, C., Van Dijck, A., Passeggeri, M., Kooy, F., Puechberty, J., Campbell, C., Sanlaville, D., Lefroy, H., Richetin, S., Pain, A., Geneviève, D., Kini, U., Le Caignec, C., Lespinasse, J., Skytte, A. B., Isidor, B., Zweier, C., Caberg, J. H. & 8 others, Delrue, M. A., Møller, R. S., Bojesen, A., Hjalgrim, H., Brasch-Andersen, C., Lemyre, E., Ousager, L. B. & Jacquemont, S., Oct 2019, In : Journal of Medical Genetics. 56, 10, p. 701-710

Research output: Contribution to journalJournal articleResearchpeer-review

Open Access
File
105 Downloads (Pure)

Is MED13L-related intellectual disability a recognizable syndrome?

Tørring, P. M., Larsen, M. J., Brasch-Andersen, C., Krogh, L. N., Kibæk, M., Laulund, L., Illum, N., Dunkhase-Heinl, U., Wiesener, A., Popp, B., Marangi, G., Hjortshøj, T. D., Ek, J., Vogel, I., Becher, N., Roos, L., Zollino, M. & Fagerberg, C. R., Feb 2019, In : European Journal of Medical Genetics. 62, 2, p. 129-136

Research output: Contribution to journalJournal articleResearchpeer-review

Open Access
File
130 Downloads (Pure)

Prostaglandin E 2 -EP 3 receptor subtype gene deletion in mother and son impairs platelet aggregation

Goharian, T. S., Fagerberg, C. R., Jensen, B. L., Graakjaer, J., Brasch-Andersen, C. & Nybo, M., Mar 2019, In : British Journal of Haematology. 184, 5, p. 851-853

Research output: Contribution to journalJournal articleResearchpeer-review

2018
2017

Genomic analyses of breast cancer progression reveal distinct routes of metastasis emergence

Krøigård, A. B., Larsen, M. J., Brasch-Andersen, C., Lænkholm, A. V., Knoop, A. S., Jensen, J. D., Bak, M., Mollenhauer, J., Thomassen, M. & Kruse, T. A., 2017, In : Scientific Reports. 7, 9 p., 43813.

Research output: Contribution to journalJournal articleResearchpeer-review

Open Access
File
202 Downloads (Pure)

The Immune Signaling Adaptor LAT Contributes to the Neuroanatomical Phenotype of 16p11.2 BP2-BP3 CNVs

16p11.2 Consortium, 5. Oct 2017, In : American Journal of Human Genetics. 101, 4, p. 564-577

Research output: Contribution to journalJournal articleResearchpeer-review

Open Access

YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction

Gabriele, M., Vulto-van Silfhout, A. T., Germain, P-L., Vitriolo, A., Kumar, R., Douglas, E., Haan, E., Kosaki, K., Takenouchi, T., Rauch, A., Steindl, K., Frengen, E., Misceo, D., Pedurupillay, C. R. J., Stromme, P., Rosenfeld, J. A., Shao, Y., Craigen, W. J., Schaaf, C. P., Rodriguez-Buritica, D. & 31 others, Farach, L., Friedman, J., Thulin, P., McLean, S. D., Nugent, K. M., Morton, J., Nicholl, J., Andrieux, J., Stray-Pedersen, A., Chambon, P., Patrier, S., Lynch, S. A., Kjaergaard, S., Tørring, P. M., Brasch-Andersen, C., Ronan, A., van Haeringen, A., Anderson, P. J., Powis, Z., Brunner, H. G., Pfundt, R., Schuurs-Hoeijmakers, J. H. M., van Bon, B. W. M., Lelieveld, S., Gilissen, C., Nillesen, W. M., Vissers, L. E. L. M., Gecz, J., Koolen, D. A., Testa, G. & de Vries, B. B. A., 2017, In : American Journal of Human Genetics. 100, 6, p. 907-925

Research output: Contribution to journalJournal articleResearchpeer-review

Open Access
File
186 Downloads (Pure)
2016

17q12 deletion and duplication syndrome in Denmark-A clinical cohort of 38 patients and review of the literature

Rasmussen, M., Vestergaard, E. M., Graakjaer, J., Petkov, Y., Bache, I., Fagerberg, C., Kibæk, M., Svaneby, D., Petersen, O. B., Brasch-Andersen, C. & Sunde, L., Nov 2016, In : American Journal of Medical Genetics. Part A. 170, 11, p. 2934-2942

Research output: Contribution to journalJournal articleResearchpeer-review

Neuralgisk amyotrofi er en overset diagnose ved akutte skuldersmerter

Translated title of the contribution: Neuralgic amyotrophy is an overlooked diagnosis by sudden onset of shoulder painJürgensen, L., Fagerberg, C., Kibæk, M. & Brasch-Andersen, C., 2016, In : Ugeskrift for Laeger. 178, 21, p. 2-3 V04160292.

Research output: Contribution to journalJournal articleResearchpeer-review

Open Access

S100A14 is a novel independent prognostic biomarker in the triple-negative breast cancer subtype

Ehmsen, S., Hansen, L. T., Bak, M., Brasch-Andersen, C., Ditzel, H. J. & Leth-Larsen, R., 1. Nov 2015, In : International Journal of Cancer. 137, 9, p. 2093-2103 11 p.

Research output: Contribution to journalJournal articleResearchpeer-review

2014

Disruption of the ASTN2 / TRIM32 locus at 9q33.1 is a risk factor in males for Autism Spectrum Disorders, ADHD and other neurodevelopmental phenotypes

Lionel, A. C., Tammimies, K., Vaags, A. K., Rosenfeld, J. A., Ahn, J. W., Merico, D., Noor, A., Runke, C. K., Pillalamarri, V. K., Carter, M. T., Gazzellone, M. J., Thiruvahindrapuram, B., Fagerberg, C. R., Laulund, L. W., Pellecchia, G., Lamoureux, S., Deshpande, C., Clayton-Smith, J., White, A. C., Leather, S. & 64 others, Trounce, J., Bedford, H. M., Hatchwell, E., Eis, P. S., Yuen, R. K. C., Walker, S., Uddin, M., Geraghty, M. T., Nikkel, S. M., Tomiak, E. M., Fernandez, B. A., Soreni, N., Crosbie, J., Arnold, P. D., Schachar, R. J., Roberts, W., Paterson, A. D., So, J., Szatmari, P., Chrysler, C., Woodbury-Smith, M., Lowry, R. B., Zwaigenbaum, L., Mandyam, D., Wei, J., Macdonald, J. R., Howe, J. L., Nalpathamkalam, T., Wang, Z., Tolson, D., Cobb, D. S., Wilks, T. M., Sorensen, M. J., Bader, P. I., An, Y., Wu, B-L., Musumeci, S. A., Romano, C., Postorivo, D., Nardone, A. M., Della Monica, M., Scarano, G., Zoccante, L., Novara, F., Zuffardi, O., Ciccone, R., Antona, V., Carella, M., Zelante, L., Cavalli, P., Poggiani, C., Cavallari, U., Argiropoulos, B., Chernos, J., Brasch-Andersen, C., Speevak, M., Fichera, M., Ogilvie, C. M., Shen, Y., Hodge, J. C., Talkowski, M. E., Stavropoulos, D. J., Marshall, C. R. & Scherer, S. W., 14. Jan 2014, In : Human Molecular Genetics. 23, 10, p. 2752-2768

Research output: Contribution to journalJournal articleResearchpeer-review

2013

The role of Glutathione S-Transferase (GST) and Claudin-1 (CLDN1) gene polymorphisms in contact sensitization: a cross-sectional study

Ross-Hansen, K., Linneberg, A. R., Johansen, JD., Hersoug, L-G., Brasch Andersen, C., Menné, T. & Thyssen, J., 2013, In : British Journal of Dermatology. 168, 4, p. 762-770

Research output: Contribution to journalJournal articleResearchpeer-review

2012

A case of microdeletion of 19p13 with intellectual disability, hypertrichosis, synophrys, and protruding front teeth

Jelsig, A. M., Brasch Andersen, C., Kibæk, M. & Fagerberg, C. R., 2012, In : European Journal of Medical Genetics. 55, 10, p. 564-7 4 p.

Research output: Contribution to journalJournal articleResearchpeer-review

A Novel Pseudo-Dicentric Variant of 16p11.2-q11.2 Contains Euchromatin from 16p11.2-p11.1 and Resembles Pathogenic Duplications of Proximal 16q

Barber, J. C. K., Brasch-Andersen, C., Maloney, V. K., Huang, S., Bateman, M. S., Graakjaer, J., Heinl, U. D. & Fagerberg, C., 2012, In : Cytogenetic and Genome Research. 139, 1, p. 59-64 6 p.

Research output: Contribution to journalJournal articleResearchpeer-review

Duplication of 7q36.3 encompassing the Sonic Hedgehog (SHH) gene is associated with congenital muscular hypertrophy

Kristensen, L. K., Kjaergaard, S., Kirchhoff, M., Kock, K., Brasch Andersen, C., Kibæk, M. & Ousager, L. B., 2012, In : European Journal of Medical Genetics. 55, 10, p. 557-60 4 p.

Research output: Contribution to journalJournal articleResearchpeer-review

Genetic polymorphisms in antioxidative enzymes are associated to FEV(1) in smokers independently of asthma

Malling, T. B. H., Sigsgaard, T., Andersen, C. B., Frischknecht, L., Andersen, H. R., Kruse, T. A., Sherson, D., Skadhauge, L. R., Thomsen, G., Baelum, J. & Omland, O., 2012, In : Clinical Respiratory Journal. 6, 1, p. 46-55

Research output: Contribution to journalJournal articleResearchpeer-review

Impact of ABCB1 Variants on Neutrophil Depression: A Pharmacogenomic Study of Paclitaxel in 92 Women with Ovarian Cancer

Bergmann, T. K., Andersen, C. B., Gréen, H., Mirza, M. R., Skougaard, K., Wihl, J., Keldsen, N., Damkier, P., Peterson, C., Vach, W. & Brøsen, K., 2012, In : Basic & Clinical Pharmacology & Toxicology. 110, 2, p. 199-204

Research output: Contribution to journalJournal articleResearchpeer-review

The relationship of Glutathione-S-Transferases copy number variation and indoor air pollution to symptoms and markers of respiratory disease

Hersoug, L-G., Andersen, C. B., Husemoen, L. L. N., Sigsgaard, T. & Linneberg, A. R., 8. Jun 2012, In : Clinical Respiratory Journal.

Research output: Contribution to journalJournal articleResearchpeer-review

Very important pharmacogene summary for VDR

Poon, A. H., Gong, L., Brasch Andersen, C., Litonjua, A. A., Raby, B. A., Hamid, Q., Laprise, C., Weiss, S. T., Altman, R. B. & Klein, T. E., 2012, In : Pharmacogenetics and Genomics. 22, 10, p. 758-63 6 p.

Research output: Contribution to journalJournal articleResearchpeer-review

2011

A BRCA2 mutation incorrectly mapped in the original BRCA2 reference sequence, is a common West Danish founder mutation disrupting mRNA splicing

Thomassen, M., Pedersen, I. S., Vogel, I., Hansen, T. V. O., Brasch-Andersen, C., Brasen, C. L., Crüger, D., Sunde, L., Nielsen, F. C., Jensen, U. B., Bisgaard, S. M. L., Borg, A., Gerdes, A-M. & Kruse, T. A., 2011, In : Breast Cancer Research and Treatment. 128, 1, p. 179-185

Research output: Contribution to journalJournal articleResearchpeer-review

Impact of CYP2C8*3 on paclitaxel clearance: a population pharmacokinetic and pharmacogenomic study in 93 patients with ovarian cancer

Bergmann, T. K., Brasch-Andersen, C., Gréen, H., Mirza, M., Pedersen, R. S., Nielsen, F., Skougaard, K., Wihl, J., Keldsen, N., Damkier, P., Friberg, L. E., Peterson, C., Vach, W., Karlsson, M. O. & Brøsen, K., 2011, In : Pharmacogenomics Journal. 11, 2, p. 113-120

Research output: Contribution to journalJournal articleResearchpeer-review

File
613 Downloads (Pure)

Retrospective study of the impact of pharmacogenetic variants on paclitaxel toxicity and survival in patients with ovarian cancer

Bergmann, T. K., Gréen, H., Andersen, C. B., Mirza, M. R., Herrstedt, J., Hølund, B., du Bois, A., Damkier, P., Vach, W., Brøsen, K. & Peterson, C., 2011, In : European Journal of Clinical Pharmacology. 67, 7, p. 693-700

Research output: Contribution to journalJournal articleResearchpeer-review

2010

Genetic susceptibility factors for multiple chemical sensitivity revisited

Berg, N. D., Berg Rasmussen, H., Linneberg, A., Brasch-Andersen, C., Fenger, M., Dirksen, A., Vesterhauge, S., Werge, T. & Elberling, J., 1. Mar 2010, In : International Journal of Hygiene and Environmental Health. 213, 2, p. 131-139 8 p.

Research output: Contribution to journalJournal articleResearchpeer-review

Linkage disequilibrium between the CYP2C19*17 allele and wildtype CYP2C8 and CYP2C9 alleles: identification of CYP2C haplotypes in healthy Nordic populations

Pedersen, R. S., Brasch Andersen, C., Sim, S. C., Bergmann, T. K., Halling, J., Petersen, M. S., Weihe, P., Edvardsen, H., Kristensen, V. N., Brøsen, K. & Ingelman-Sundberg, M., 2010, In : European Journal of Clinical Pharmacology. 66, 12, p. 1199-1205

Research output: Contribution to journalJournal articleResearchpeer-review

2009

Linkage of atopic dermatitis to chromosomes 4q22, 3p24 and 3q21

Christensen, U., Møller-Larsen, S., Nyegaard, M., Haagerup, A., Hedemand, A., Brasch-Andersen, C., Kruse, T., Corydon, T., Deleuran, M. & Børglum, A., 11. Jun 2009, In : Human Genetics. 126, 4, p. 549-557

Research output: Contribution to journalJournal articleResearchpeer-review

The interaction of glutathione S-transferase M1-null variants with tobacco smoke exposure and the development of childhood asthma

Rogers, A. J., Brasch-Andersen, C., Ionita-Laza, I., Murphy, A., Sharma, S., Klanderman, B. J. & Raby, B. A., 1. Nov 2009, In : Clinical and Experimental Allergy. 39, 11, p. 1721-1729 8 p.

Research output: Contribution to journalJournal articleResearchpeer-review

2008

Evidence for an asthma risk locus on chromosome Xp: a replication linkage study

Brasch-Andersen, C., Møller, M. U., Haagerup, A., Vestbo, J. & Kruse, T. A., 1. Sep 2008, In : Allergy. European Journal of Allergy and Clinical Immunology. 63, 9, p. 1235-8 3 p.

Research output: Contribution to journalJournal articleResearchpeer-review

2007

Interactions between GSTM1, GSTT1 and GSTP1 polymorphisms and smoking and intake of fruit and vegetables in relation to lung cancer

Sørensen, M., Raaschou-Nielsen, O., Brasch-Andersen, C., Tjønneland, A., Overvad, K. & Autrup, H., 1. Feb 2007, In : Lung Cancer. 55, 2, p. 137-144 7 p.

Research output: Contribution to journalJournal articleResearchpeer-review

Retrospective analysis of main and interaction effects in genetic association studies of human complex traits

Tan, Q., Christiansen, L., Brasch-Andersen, C., Zhao, J. H., Li, S., Kruse, T. A. & Christensen, K., 2007, In : BMC Genetics. 8, p. 70

Research output: Contribution to journalJournal articleResearchpeer-review

2006

A longitudinal study of the effect of GSTT1 and GSTM1 gene copy number on survival

Christiansen, L., Andersen, C. B., Bathum, L., Kruse, T. & Christensen, K., 2006, In : Mechanisms of Ageing and Development. 127, 7, p. 597-599

Research output: Contribution to journalJournal articleResearchpeer-review

Highly significant linkage to chromosome 3q13.31 for rhinitis and related allergic diseases

Andersen, C. B., Haagerup, A., Børglum, A. D., Vestbo, J. & Kruse, T., 2006, In : Journal of Medical Genetics. 43, 3, p. e10

Research output: Contribution to journalJournal articleResearchpeer-review

Significant linkage to chromosome 12q24.32-q24.33 and identification of SFRS8 as a possible asthma susceptibility gene

Andersen, C. B., Tan, Q., Børglum, A. D., Haagerup, A., Larsen, T. R., Vestbo, J. & Kruse, T., 2006, In : Thorax. 61, 10, p. 874-879

Research output: Contribution to journalJournal articleResearchpeer-review

Skin manifestations in a case of trisomy 16 mosaicism

Ousager, L. B., Brandrup, F., Andersen, C. B. & Erlandsson, A., 2006, In : British Journal of Dermatology. 154, 1, p. 172-6

Research output: Contribution to journalJournal articleResearchpeer-review

2004

Possible gene dosage effect of glutathione-S-transferases on atopic asthma: Using real-time PCR for quantification of GSTM1 and GSTT1 gene copy numbers

Andersen, C. B., Christiansen, L., Tan, Q., Haagerup, A., Vestbo, J. & Kruse, T., 1. Sep 2004, In : Human Mutation. 24, 3, p. 208-214

Research output: Contribution to journalJournal articleResearchpeer-review

2002

Analysis of the polymorphic CAG repeat length in the androgen receptor gene in patients with testicular germ cell cancer

Rajpert-De Meyts, E., Leffers, H., Daugaard, G., Andersen, C. B., Petersen, P. M., Hinrichsen, J., Pedersen, L. G. & Skakkebæk, N. E., 2002, In : International Journal of Cancer. 102, p. 201-4

Research output: Contribution to journalJournal articleResearchpeer-review