A. Norberg

发表

On-line multi-analyzer monitoring of biomass, glucose and acetate for growth rate control of a Vibrio cholerae fed-batch cultivation.

Carl-Fredrik Mandenius, Anna Norberg, C. Mandenius, 2005, Journal of biotechnology.

Bacterial microbiota composition of Ixodes ricinus ticks: the role of environmental variation, tick characteristics and microbial interactions

A. Norberg, B. Tschirren, Tuomas Aivelo, 2019, bioRxiv.

Novel mutations in CRB1 and ABCA4 genes cause Leber congenital amaurosis and Stargardt disease in a Swedish family

O. Sandgren, I. Golovleva, A. Norberg, 2013, European Journal of Human Genetics.

Intraspecific host variation plays a key role in virus community assembly

Anna‐Liisa Laine, A. Norberg, H. Susi, 2020, Nature Communications.

Characterization of an X-chromosome-linked telomere biology disorder in females with DKC1 mutation

O. Kilpivaara, A. Norberg, K. Hannula-Jouppi, 2018, Leukemia.

Exclusion of the juvenile myoclonic epilepsy gene EFHC1 as the cause of migraine on chromosome 6, but association to two rare polymorphisms in MEP1A and RHAG

L. Forsgren, M. Holmberg, D. Holmberg, 2006, Neuroscience Letters.

Genetic heterogeneity and clinical outcome in a Swedish family with retinal degeneration caused by mutations in CRB1 and ABCA4 genes.

O. Sandgren, I. Golovleva, A. Norberg, 2014, Advances in experimental medicine and biology.

Direct and indirect viral associations predict coexistence in wild plant virus communities

N. Clark, Anna‐Liisa Laine, A. Norberg, 2021, Current Biology.

A mutation in the H/ACA box of telomerase RNA component gene (TERC) in a young patient with myelodysplastic syndrome

S. Kajigaya, N. Young, R. Calado, 2014, BMC Medical Genetics.

Nerve growth factor R221W responsible for insensitivity to pain is defectively processed and accumulates as proNGF

M. Holmberg, E. Larsson, J. Minde, 2009, Neurobiology of Disease.

Author's response to reviews Title:A mutation in H/ACA box of telomerase RNA component gene (TERC) in a young patient with myelodysplastic syndrome Authors:

S. Kajigaya, R. Calado, E. Hellstrôm-Lindberg, 2014 .

Biallelic mutations in WRAP53 result in dysfunctional telomeres, Cajal bodies and DNA repair, thereby causing Hoyeraal–Hreidarsson syndrome

A. Nordgren, S. Böhm, H. Malmgren, 2020, Cell Death & Disease.

Spatially structured eco-evolutionary dynamics in a host-pathogen interaction render isolated populations vulnerable to disease

M. Boots, B. Ashby, Anna‐Liisa Laine, 2022, Nature Communications.

Frequent false‐negative FIP1L1‐PDGFRA FISH analyses of bone marrow samples from clonal eosinophilia at diagnosis

B. Johansson, H. Sjögren, A. Norberg, 2019, British journal of haematology.

How to make more out of community data? A conceptual framework and its implementation as models and software.

Anna Norberg, David Dunson, Otso Ovaskainen, 2017, Ecology letters.

A comprehensive evaluation of predictive performance of 33 species distribution models at species and community levels

David B. Dunson, Jane Elith, Antoine Guisan, 2019, Ecological Monographs.

Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing

S. Jensen, A. Rydberg, A. Winbo, 2012, BMC Cardiovascular Disorders.

Genetic screening in sudden cardiac death in the young can save future lives

S. Mörner, J. Jonasson, K. Cederquist, 2015, International Journal of Legal Medicine.

Bacterial microbiota composition of Ixodes ricinus ticks: the role of environmental variation, tick characteristics and microbial interactions

A. Norberg, B. Tschirren, Tuomas Aivelo, 2019, bioRxiv.

Novel variants in Nordic patients referred for genetic testing of telomere-related disorders

L. Kjeldsen, G. Roos, O. Lohi, 2018, European Journal of Human Genetics.

Diagnostics of rare disorders

J. Casanova, K. Jahnukainen, J. Saarela, 2022 .

Parasite-microbiota interactions potentially affect intestinal communities in wild mammals

A. Norberg, Tuomas Aivelo, 2016, bioRxiv.

cross-immunity preventing the colonization of different microbes with similar antigenic properties

A. Norberg, B. Tschirren, Tuomas Aivelo, 2019 .

Sex is a moderator of the association between NOS1AP sequence variants and QTc in two long QT syndrome founder populations: a pedigree-based measured genotype association analysis

S. Jensen, A. Rydberg, A. Winbo, 2017, BMC Medical Genetics.

Diagnostics of rare disorders: whole-exome sequencing deciphering locus heterogeneity in telomere biology disorders

J. Casanova, K. Jahnukainen, J. Saarela, 2018, Orphanet Journal of Rare Diseases.

Congenital dyserythropoietic anemia type III (CDA III) is caused by a mutation in kinesin family member, KIF23.

A. Wåhlin, I. Golovleva, A. Norberg, 2013, Blood.

Evaluating Functional Diversity: Missing Trait Data and the Importance of Species Abundance Structure and Data Transformation

K. Sam, M. Bryndová, J. Lepš, 2016, PloS one.

Measuring and predicting the influence of traits on the assembly processes of wood‐inhabiting fungi

Anna Norberg, Otso Ovaskainen, Nerea Abrego, 2017 .

Experimentally induced community assembly of polypores reveals the importance of both environmental filtering and assembly history

J. S. Kotiaho, O. Ovaskainen, Tero Toivanen, 2019, Fungal Ecology.

Spore production monitoring reveals contrasting seasonal strategies and a trade‐off between spore size and number in wood‐inhabiting fungi

O. Ovaskainen, P. Halme, A. Norberg, 2023, Functional Ecology.

Parasite-microbiota interactions potentially affect intestinal communities in wild mammals

A. Norberg, Tuomas Aivelo, 2016, bioRxiv.

DNA methylation variations and epigenetic aging in telomere biology disorders

M. Landfors, A. Norberg, M. Hultdin, 2023, Scientific reports.

Novel variants in Nordic patients referred for genetic testing of telomere-related disorders

L. Kjeldsen, G. Roos, O. Lohi, 2018, European Journal of Human Genetics.

Genetic Subtypes and Outcome of Patients Aged 1 to 45 Years Old With Acute Lymphoblastic Leukemia in the NOPHO ALL2008 Trial

B. Johansson, E. Kjeldsen, P. Tammur, 2023, HemaSphere.

Human pathogen co-occurrence in Ixodes ricinus ticks: effects of landscape topography, 1 climatic factors and microbiota interactions 2

A. Norberg, B. Tschirren, Tuomas Aivelo, 2019 .

Novel pathological variants of NHP2 affect N-terminal domain flexibility, protein stability, H/ACA Ribonucleoprotein (RNP) complex formation and telomerase activity

C. Ladenvall, J. Vertemara, P. Baliakas, 2023, Human molecular genetics.