Publications by authors named "Tiina Berg"

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Human Bacterial Artificial Chromosome (BAC) Transgenesis Fully Rescues Noradrenergic Function in Dopamine β-Hydroxylase Knockout Mice.
Joseph F Cubells, Jason P Schroeder, Elizabeth S Barrie, Daniel F Manvich, Wolfgang Sadee, Tiina Berg

PLoS One· July 2017

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Whole-exome sequencing identifies novel MPL and JAK2 mutations in triple-negative myeloproliferative neoplasms.
Jelena D Milosevic Feenstra, Harini Nivarthi, Heinz Gisslinger, Emilie Leroy, Elisa Rumi, Tiina Berg

Blood· January 2016

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Germline RBBP6 mutations in familial myeloproliferative neoplasms.
Ashot S Harutyunyan, Roberto Giambruno, Christian Krendl, Alexey Stukalov, Thorsten Klampfl, Tiina Berg

Blood· January 2016

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Molecular responses and chromosomal aberrations in patients with polycythemia vera treated with peg-proline-interferon alpha-2b.
Nicole C C Them, Klaudia Bagienski, Tiina Berg, Bettina Gisslinger, Martin Schalling

Am J Hematol· April 2015

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Common germline variation at the TERT locus contributes to familial clustering of myeloproliferative neoplasms.
Roland Jäger, Ashot S Harutyunyan, Elisa Rumi, Daniela Pietra, Tiina Berg

Am J Hematol· December 2014

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Complex patterns of chromosome 11 aberrations in myeloid malignancies target CBL, MLL, DDB1 and LMO2.
Thorsten Klampfl, Jelena D Milosevic, Ana Puda, Andreas Schönegger, Klaudia Bagienski, Tiina Berg

PLoS One· June 2014

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The triggering receptor expressed on myeloid cells 2 inhibits complement component 1q effector mechanisms and exerts detrimental effects during pneumococcal pneumonia.
Omar Sharif, Riem Gawish, Joanna M Warszawska, Rui Martins, Karin Lakovits, Tiina Berg

PLoS Pathog· June 2014

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CALR exon 9 mutations are somatically acquired events in familial cases of essential thrombocythemia or primary myelofibrosis.
Elisa Rumi, Ashot S Harutyunyan, Daniela Pietra, Jelena D Milosevic, Ilaria C Casetti, Tiina Berg

Blood· April 2014

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JAK2 or CALR mutation status defines subtypes of essential thrombocythemia with substantially different clinical course and outcomes.
Elisa Rumi, Daniela Pietra, Virginia Ferretti, Thorsten Klampfl, Ashot S Harutyunyan, Tiina Berg

Blood· March 2014

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A novel germline JAK2 mutation in familial myeloproliferative neoplasms.
Elisa Rumi, Ashot S Harutyunyan, Ilaria Casetti, Daniela Pietra, Harini Nivarthi, Tiina Berg

Am J Hematol· January 2014

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Somatic mutations of calreticulin in myeloproliferative neoplasms.
Thorsten Klampfl, Heinz Gisslinger, Ashot S Harutyunyan, Harini Nivarthi, Elisa Rumi, Tiina Berg

N Engl J Med· December 2013

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Clinical significance of genetic aberrations in secondary acute myeloid leukemia.
Jelena D Milosevic, Ana Puda, Luca Malcovati, Tiina Berg, Michael Hofbauer

Am J Hematol· November 2012

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Frequent deletions of JARID2 in leukemic transformation of chronic myeloid malignancies.
Ana Puda, Jelena D Milosevic, Tiina Berg, Thorsten Klampfl, Ashot S Harutyunyan

Am J Hematol· March 2012

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Functional dissection of the TBK1 molecular network.
Adriana Goncalves, Tilmann Bürckstümmer, Evelyn Dixit, Ruth Scheicher, Maria W Górna, Tiina Berg

PLoS One· February 2012

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Identification of genomic aberrations associated with disease transformation by means of high-resolution SNP array analysis in patients with myeloproliferative neoplasm.
Elisa Rumi, Ashot Harutyunyan, Chiara Elena, Daniela Pietra, Thorsten Klampfl, Tiina Berg

Am J Hematol· December 2011

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Genome integrity of myeloproliferative neoplasms in chronic phase and during disease progression.
Thorsten Klampfl, Ashot Harutyunyan, Tiina Berg, Bettina Gisslinger, Martin Schalling

Blood· July 2011

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The role of the JAK2 GGCC haplotype and the TET2 gene in familial myeloproliferative neoplasms.
Damla Olcaydu, Elisa Rumi, Ashot Harutyunyan, Francesco Passamonti, Daniela Pietra, Tiina Berg

Haematologica· March 2011

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A common JAK2 haplotype confers susceptibility to myeloproliferative neoplasms.
Damla Olcaydu, Ashot Harutyunyan, Roland Jäger, Tiina Berg, Bettina Gisslinger

Nat Genet· April 2009

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Acquired resistance to interferon alpha therapy associated with homozygous MPL-W515L mutation and chromosome 20q deletion in primary myelofibrosis.
Veronika Buxhofer-Ausch, Heinz Gisslinger, Tiina Berg, Bettina Gisslinger, Robert Kralovics

Eur J Haematol· February 2009

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Influence of child abuse on adult depression: moderation by the corticotropin-releasing hormone receptor gene.
Rebekah G Bradley, Elisabeth B Binder, Michael P Epstein, Yilang Tang, Hemu P Nair, Tiina Berg

Arch Gen Psychiatry· February 2008

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Polymorphisms in the novel gene acyloxyacyl hydroxylase (AOAH) are associated with asthma and associated phenotypes.
Kathleen C Barnes, Audrey Grant, Peisong Gao, Daniela Baltadjieva, Tiina Berg

J Allergy Clin Immunol· July 2006

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