Karin Wallander

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About me

My main interest is oncogenetics. I am a specialist medical doctor in clinical genetics, focusing on hereditary cancer syndromes. After defending my thesis at Karolinska Institutet, Stockholm, I spent 6 months at IDIBAPS, Hospital Clinic, Barcelona, performing CRISPR-Cas9 knock-in. Since then, I have joined Felix Haglund de Flon's research group as a post-doc, evaluating whole-genome and whole-transcriptome sequencing for sarcoma diagnostics. Cancerfonden (the Swedish cancer society) has awarded me a full-time three year post-doc fellowship for this.

Articles

Article: CLINICAL CANCER RESEARCH. 2024;30(12):2647-2658
Comprehensive Genomic Profiling Alters Clinical Diagnoses in a Significant Fraction of Tumors Suspicious of Sarcoma
Ofverholm I; Wallander K; Haglund C; Chellappa V; Wejde J; Gellerbring A; Wirta V; Renevey A; Caceres E; Tsagkozis P; Mayrhofer M; Papakonstantinou A; Linder-Stragliotto C; Branstrom R; Larsson O; Lindberg J; Lin Y; de Flon FH
Journal article: ESMO OPEN. 2023;8(1):101095
58P Evaluating the impact of WGTS in routine diagnostics of bone and soft tissue tumors
Wallander KM; Öfverholm I; Yingbo L; Haglund C; Chellappa V; Tsagkozis P; Hesla A; Papakonstantinou A; Bränström R; Wirta V; Lindberg J; de Flon FH
Article: CANCERS. 2023;15(4):1160
Sensitive Detection of Cell-Free Tumour DNA Using Optimised Targeted Sequencing Can Predict Prognosis in Gastro-Oesophageal Cancer
Wallander K; Haider Z; Jeggari A; Foroughi-Asl H; Gellerbring A; Lyander A; Chozhan A; Gyllensten OC; Haegglund M; Wirta V; Nordenskjoeld M; Lindblad M; Tham E
Article: HEREDITARY CANCER IN CLINICAL PRACTICE. 2021;19(1):46
Massive parallel sequencing in individuals with multiple primary tumours reveals the benefit of re-analysis
Wallander K; Thonberg H; Nilsson D; Tham E
Article: HEREDITARY CANCER IN CLINICAL PRACTICE. 2021;19(1):23
Massive parallel sequencing in a family with rectal cancer
Wallander K; Thutkawkorapin J; Sahlin E; Lindblom A; Lagerstedt-Robinson K
Article: PLOS ONE. 2021;16(2):e0245488
Cell-free tumour DNA analysis detects copy number alterations in gastro-oesophageal cancer patients
Wallander K; Eisfeldt J; Lindblad M; Nilsson D; Billiau K; Foroughi H; Nordenskjold M; Lieden A; Tham E
Article: GENES CHROMOSOMES AND CANCER. 2019;58(11):775-782
Genetic analyses supporting colorectal, gastric, and prostate cancer syndromes
Wallander K; Liu W; von Holst S; Thutkawkorapin J; Kontham V; Forsberg A; Lindblom A; Lagerstedt-Robinson K
Article: GENETICS IN MEDICINE. 2018;20(4):452-457
Individuals with &ITFANCM&IT biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility
Catucci I; Osorio A; Arver B; Neidhardt G; Bogliolo M; Zanardi F; Riboni M; Minardi S; Pujol R; Azzollini J; Peissel B; Manoukian S; De Vecchi G; Casola S; Hauke J; Richters L; Rhiem K; Schmutzler RK; Wallander K; Torngren T; Borg A; Radice P; Surralles J; Hahnen E; Ehrencrona H; Kvist A; Benitez J; Peterlongo P
Article: NEUROPEDIATRICS. 2014;45(6):362-370
Zonisamide: Pharmacokinetics, Efficacy, and Adverse Events in Children with Epilepsy
Wallander KM; Ohman I; Dahlin M

All other publications

Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2024;32:549-550
SarcDBase: a tool for detection of genetic alterations in sarcoma
Difilippo V; Saba K; Wallander K; Nathrath M; Baumhoer D; Haglund F; Nord KH
Review: JOURNAL OF INTERNAL MEDICINE. 2023;294(6):690-707
Sarcoma care in the era of precision medicine
Wallander K; Ofverholm I; Boye K; Tsagkozis P; Papakonstantinou A; Lin Y; de Flon FH
Conference publication: KLINISCHE PADIATRIE. 2023;235(3):193
SarcDBase: a tool for detection of genetic alterations in sarcoma
Difilippo V; Saba KH; Wallander K; Nathrath M; Baumhoer D; de Flon HF; Nord KH
Thesis / dissertation: 2021
Hereditary predisposition and prognostic prediction in cancer
Wallander, Karin
Corrigendum: HEREDITARY CANCER IN CLINICAL PRACTICE. 2021;19(1):47
Massive parallel sequencing in individuals with multiple primary tumours reveals the benefit of re-analysis (vol 19, 46, 2021)
Wallander K; Thonberg H; Nilsson D; Tham E
Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2020;28(SUPPL 1):526-527
Cellfree tumour DNA analysis detects copy number alterations in gastrooesophageal cancer patients.
Wallander K; Eisfeldt J; Lindblad M; Nilsson D; Billiau K; Foroughi H; Nordenskjold M; Leiden A; Tham E
Review: JOURNAL OF INTERNAL MEDICINE. 2019;286(2):118-136
Cell-free tumour DNA testing for early detection of cancer - a potential future tool
Barbany G; Arthur C; Lieden A; Nordenskjold M; Rosenquist R; Tesi B; Wallander K; Tham E
Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2018;26:587-588
Whole genome sequencing in patients with multiple primary tumors
Wallander K; Nilsson D; Tham E

Employments

Affiliated to Research, Department of Oncology-Pathology, Karolinska Institutet, 2023-2025

Degrees and Education

Degree Of Doctor Of Philosophy, Department of Molecular Medicine and Surgery, Karolinska Institutet, 2022

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