Publications by authors named "Anna Rohlin"

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High baseline PD-1+ CD8 T Cells and TIGIT+ CD8 T Cells in circulation associated with response to PD-1 blockade in patients with non-small cell lung cancer.
Nikita Dutta, Johanna Svensson, George-Alehandro Saad, Marielle Mello, Ella A Eklund, Anna Rohlin

Cancer Immunol Immunother· September 2025

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Comprehensive genetic variant analysis reveals combination of KRAS and LRP1B as a predictive biomarker of response to immunotherapy in patients with non-small cell lung cancer.
Ella A Eklund, Johanna Svensson, Louise Stauber Näslund, Maria Yhr, Sama I Sayin, Anna Rohlin

J Exp Clin Cancer Res· February 2025

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A national long-read sequencing study on chromosomal rearrangements uncovers hidden complexities.
Jesper Eisfeldt, Adam Ameur, Felix Lenner, Esmee Ten Berk de Boer, Marlene Ek, Anna Rohlin

Genome Res· November 2024

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The value of genome-wide analysis in craniosynostosis.
Alexandra Topa, Anna Rohlin, André Fehr, Lovisa Lovmar, Göran Stenman

Front Genet· January 2024

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Combinatory analysis of immune cell subsets and tumor-specific genetic variants predict clinical response to PD-1 blockade in patients with non-small cell lung cancer.
Nikita Dutta, Anna Rohlin, Ella A Eklund, Maria K Magnusson, Frida Nilsson

Front Oncol· February 2023

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Merged testing for colorectal cancer syndromes and re-evaluation of genetic variants improve diagnostic yield: Results from a nationwide prospective cohort.
Sara Svensson, Theofanis Zagoras, Christos Aravidis, Marie Stenmark Askmalm, Erik Björck, Anna Rohlin

Genes Chromosomes Cancer· October 2022

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The outcome of targeted NGS screening in patients with syndromic forms of sagittal and pansynostosis - IL11RA is an emerging core-gene for pansynostosis.
Alexandra Topa, Anna Rohlin, Mattias K Andersson, André Fehr, Lovisa Lovmar

Eur J Med Genet· May 2022

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PΨFinder: a practical tool for the identification and visualization of novel pseudogenes in DNA sequencing data.
Sanna Abrahamsson, Frida Eiengård, Anna Rohlin, Marcela Dávila López

BMC Bioinformatics· February 2022

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Identification of known and novel familial cancer genes in Swedish colorectal cancer families.
Hafdis T Helgadottir, Jessada Thutkawkorapin, Anna Rohlin, Margareta Nordling, Kristina Lagerstedt-Robinson

Int J Cancer· August 2021

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Immune checkpoint blockade and biomarkers of clinical response in non-small cell lung cancer.
Andreas Hallqvist, Anna Rohlin, Sukanya Raghavan

Scand J Immunol· December 2020

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NGS targeted screening of 100 Scandinavian patients with coronal synostosis.
Alexandra Topa, Anna Rohlin, Mattias K Andersson, André Fehr, Lovisa Lovmar

Am J Med Genet A· February 2020

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Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition.
Alisa Olkinuora, Taina T Nieminen, Emma Mårtensson, Anna Rohlin, Ari Ristimäki

Genet Med· August 2019

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Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing.
Anna Rohlin, Eva Rambech, Anders Kvist, Therese Törngren, Frida Eiengård

Fam Cancer· April 2017

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Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
Kristina Lagerstedt-Robinson, Anna Rohlin, Christos Aravidis, Beatrice Melin, Margareta Nordling

Oncol Rep· November 2016

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GREM1 and POLE variants in hereditary colorectal cancer syndromes.
Anna Rohlin, Frida Eiengård, Ulf Lundstam, Theofanis Zagoras, Staffan Nilsson

Genes Chromosomes Cancer· January 2016

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A mutation in POLE predisposing to a multi-tumour phenotype.
Anna Rohlin, Theofanis Zagoras, Staffan Nilsson, Ulf Lundstam, Jan Wahlström

Int J Oncol· July 2014

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Parallel sequencing used in detection of mosaic mutations: comparison with four diagnostic DNA screening techniques.
Anna Rohlin, Josephine Wernersson, Yvonne Engwall, Leif Wiklund, Jan Björk

Hum Mutat· June 2009

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Clinical characterization and the mutation spectrum in Swedish adenomatous polyposis families.
Gunilla Kanter-Smoler, Kaisa Fritzell, Anna Rohlin, Yvonne Engwall, Birgitta Hallberg

BMC Med· April 2008

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