Exome sequencing in 51 early onset non‐familial CRC cases

por Thutkawkorapin, Jessada, Lindblom, Annika, Tham, Emma
Publicado 2019

pyCancerSig: subclassifying human cancer with comprehensive single nucleotide, structural and microsatellite mutational signature deconstruction from whole genome sequencing

por Thutkawkorapin, Jessada, Eisfeldt, Jesper, Tham, Emma, Nilsson, Daniel
Publicado 2020

Massive parallel sequencing in individuals with multiple primary tumours reveals the benefit of re-analysis

por Wallander, Karin, Thonberg, Håkan, Nilsson, Daniel, Tham, Emma
Publicado 2021

Correction to: Massive parallel sequencing in individuals with multiple primary tumours reveals the benefit of re-analysis

por Wallander, Karin, Thonberg, Håkan, Nilsson, Daniel, Tham, Emma
Publicado 2021

Screening for germline phosphatase and tensin homolog-mutations in suspected Cowden syndrome and Cowden syndrome-like families among uterine cancer patients

por TZORTZATOS, GERASIMOS, ARAVIDIS, CHRISTOS, LINDBLOM, ANNIKA, MINTS, MIRIAM, THAM, EMMA
Publicado 2015

Patient-specific targeted analysis of circulating tumour DNA in plasma is feasible and may be a potential biomarker in UTUC

por Mu, Ninni, Jylhä, Cecilia, Axelsson, Tomas, Sydén, Filip, Brehmer, Marianne, Tham, Emma
Publicado 2023

Familial cancer among consecutive uterine cancer patients in Sweden

por Tzortzatos, Gerasimos, Wersäll, Ofra, Danielsson, Kristina Gemzell, Lindblom, Annika, Tham, Emma, Mints, Miriam
Publicado 2014

Transposable element insertions in 1000 Swedish individuals

por Bilgrav Saether, Kristine, Nilsson, Daniel, Thonberg, Håkan, Tham, Emma, Ameur, Adam, Eisfeldt, Jesper, Lindstrand, Anna
Publicado 2023

Whole-body MRI within a surveillance program for carriers with clinically actionable germline TP53 variants - the Swedish constitutional TP53 study SWEP53

por Omran, Meis, Blomqvist, Lennart, Brandberg, Yvonne, Pal, Niklas, Kogner, Per, Ståhlbom, Anne Kinhult, Tham, Emma, Bajalica-Lagercrantz, Svetlana
Publicado 2020

Cell-free tumour DNA analysis detects copy number alterations in gastro-oesophageal cancer patients

por Wallander, Karin, Eisfeldt, Jesper, Lindblad, Mats, Nilsson, Daniel, Billiau, Kenny, Foroughi, Hassan, Nordenskjöld, Magnus, Liedén, Agne, Tham, Emma
Publicado 2021

Patient-Specific Assays Based on Whole-Genome Sequencing Data to Measure Residual Disease in Children With Acute Lymphoblastic Leukemia: A Proof of Concept Study

por Arthur, Cecilia, Rezayee, Fatemah, Mogensen, Nina, Saft, Leonie, Rosenquist, Richard, Nordenskjöld, Magnus, Harila-Saari, Arja, Tham, Emma, Barbany, Gisela
Publicado 2022

Public support for healthcare-mediated disclosure of hereditary cancer risk information: Results from a population-based survey in Sweden

por Andersson, Andreas, Hawranek, Carolina, Öfverholm, Anna, Ehrencrona, Hans, Grill, Kalle, Hajdarevic, Senada, Melin, Beatrice, Tham, Emma, Hellquist, Barbro Numan, Rosén, Anna
Publicado 2020

The Expression of VEGF-A Is Down Regulated in Peripheral Blood Mononuclear Cells of Patients with Secondary Progressive Multiple Sclerosis

por Iacobaeus, Ellen, Amoudruz, Petra, Ström, Mikael, Khademi, Mohsen, Brundin, Lou, Hillert, Jan, Kockum, Ingrid, Malmström, Vivianne, Olsson, Tomas, Tham, Emma, Piehl, Fredrik
Publicado 2011

Simultaneous Ultra-Sensitive Detection of Structural and Single Nucleotide Variants Using Multiplex Droplet Digital PCR in Liquid Biopsies from Children with Medulloblastoma

por Arthur, Cecilia, Jylhä, Cecilia, de Ståhl, Teresita Díaz, Shamikh, Alia, Sandgren, Johanna, Rosenquist, Richard, Nordenskjöld, Magnus, Harila, Arja, Barbany, Gisela, Sandvik, Ulrika, Tham, Emma
Publicado 2023

A retrospective two centre study of Birt-Hogg-Dubé syndrome reveals a pathogenic founder mutation in FLCN in the Swedish population

por Lagerstedt-Robinson, Kristina, Baranowska Körberg, Izabella, Tsiaprazis, Stefanos, Björck, Erik, Tham, Emma, Poluha, Anna, Hellström Pigg, Maritta, Paulsson-Karlsson, Ylva, Nordenskjöld, Magnus, Johansson-Soller, Maria, Aravidis, Christos
Publicado 2022

Sensitive Detection of Cell-Free Tumour DNA Using Optimised Targeted Sequencing Can Predict Prognosis in Gastro-Oesophageal Cancer

por Wallander, Karin, Haider, Zahra, Jeggari, Ashwini, Foroughi-Asl, Hassan, Gellerbring, Anna, Lyander, Anna, Chozhan, Athithyan, Cuba Gyllensten, Ollanta, Hägglund, Moa, Wirta, Valtteri, Nordenskjöld, Magnus, Lindblad, Mats, Tham, Emma
Publicado 2023

A retrospective study of extracolonic, non-endometrial cancer in Swedish Lynch syndrome families

por Karimi, Masoud, von Salomé, Jenny, Aravidis, Christos, Silander, Gustav, Askmalm, Marie Stenmark, Henriksson, Isabelle, Gebre-Medhin, Samuel, Frödin, Jan-Erik, Björck, Erik, Lagerstedt-Robinson, Kristina, Lindblom, Annika, Tham, Emma
Publicado 2018

Consultation on UTUC II Stockholm 2022: diagnostic and prognostic methods—what’s around the corner?

por Grahn, Alexandra, Coleman, Jonathan A., Eriksson, Ylva, Gabrielsson, Susanne, Madsen, Jonna Skov, Tham, Emma, Thomas, Kay, Turney, Ben, Uhlén, Per, Vollmer, Tino, Zieger, Karsten, Osther, Palle Jörn Sloth, Brehmer, Marianne
Publicado 2023

Whole-Body MRI Surveillance—Baseline Findings in the Swedish Multicentre Hereditary TP53-Related Cancer Syndrome Study (SWEP53)

por Omran, Meis, Tham, Emma, Brandberg, Yvonne, Ahlström, Håkan, Lundgren, Claudia, Paulsson-Karlsson, Ylva, Kuchinskaya, Ekaterina, Silander, Gustav, Rosén, Anna, Persson, Fredrik, Leonhardt, Henrik, Stenmark-Askmalm, Marie, Berg, Johanna, van Westen, Danielle, Bajalica-Lagercrantz, Svetlana, Blomqvist, Lennart
Publicado 2022

The MLH1 polymorphism rs1800734 and risk of endometrial cancer with microsatellite instability

por Russell, Holly, Kedzierska, Katarzyna, Buchanan, Daniel D., Thomas, Rachael, Tham, Emma, Mints, Miriam, Keränen, Anne, Giles, Graham G., Southey, Melissa C., Milne, Roger L., Tomlinson, Ian, Church, David, Spurdle, Amanda B., O’Mara, Tracy A., Lewis, Annabelle
Publicado 2020