P. Söderkvist

J. Lundeberg, G. Pershagen, P. Söderkvist, 1999, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Mutations in the isocitrate dehydrogenase 2 gene and IDH1 SNP 105C > T have a prognostic value in acute myeloid leukemia

P. Söderkvist, E. Paul, M. Hermansson, 2014, Biomarker Research.

PIK3CA, HRAS and KRAS gene mutations in human penile cancer.

P. Söderkvist, T. Windahl, Peter Kirrander, 2008, The Journal of urology.

K‐ras and B‐raf gene mutations are not associated with gastrin‐ and CCK2‐receptor mRNA expression in human colorectal tumour tissues

K. Fransén, P. Söderkvist, H. Monstein, 2004, European journal of clinical investigation.

Association between TERT promoter polymorphisms and acute myeloid leukemia risk and prognosis

M. Höglund, P. Söderkvist, Mohamed Ali Mosrati, 2015, Oncotarget.

Characterization of sequence variations in human histone H1.2 and H1.4 subtypes

B. Sarg, H. Lindner, P. Söderkvist, 2005, The FEBS journal.

Glucocerebrosidase variant T369M is not a risk factor for Parkinson’s disease in Sweden

P. Svenningsson, K. Wirdefeldt, P. Söderkvist, 2022, Neuroscience Letters.

Activation of RAS Signalling is Associated with Altered Cell Adhesion in Phaeochromocytoma

C. Larsson, P. Söderkvist, O. Gimm, 2020, International journal of molecular sciences.

Increased diagnostic sensitivity of palpation‐guided thyroid nodule fine‐needle aspiration cytology by BRAF V600E‐mutation analysis

P. Söderkvist, O. Gimm, S. Garvin, 2021, The journal of pathology. Clinical research.

Pharmacogenetic studies of Paclitaxel in the treatment of ovarian cancer.

P. Söderkvist, H. Gréen, P. Rymark, 2009, Basic & clinical pharmacology & toxicology.

Hypoxia Signaling and Circadian Disruption in and by Pheochromocytoma

P. Söderkvist, Mouna Tabebi, Lasse D Jensen, 2018, Front. Endocrinol..

Extent of surgery for phaeochromocytomas in the genomic era

P. Söderkvist, O. Gimm, H. M. Rossitti, 2018, The British journal of surgery.

Genetic analysis of Raf1, Mdm2, c-Myc, Cdc25a and Cdc25b proto-oncogenes in 2',3'-dideoxycytidine- and 1,3-butadiene-induced lymphomas in B6C3F1 mice.

P. Söderkvist, S. Zhuang, Peter Söderkvist, 2000, Mutation research.

Enhanced expression of cyclooxygenase-2 and nuclear beta-catenin are related to mutations in the APC gene in human colorectal cancer.

P. Söderkvist, A. Sirsjö, J. Dimberg, 2001, Anticancer research.

HRAS mutation prevalence and associated expression patterns in pheochromocytoma

C. Larsson, M. Bäckdahl, P. Söderkvist, 2016, Genes, chromosomes & cancer.

Immunohistochemical NF1 Analysis Does not Predict NF1 Gene Mutation Status in Pheochromocytoma

P. Söderkvist, A. Stenman, O. Gimm, 2015, Endocrine Pathology.

Telomerase activity in surgical specimens and fine-needle aspiration biopsies from hyperplastic and neoplastic human thyroid tissues.

P. Söderkvist, A. Herder, S. Smeds, 2003, American journal of surgery.

Association of EBF1, FAM167A(C8orf13)-BLK and TNFSF4 gene variants with primary Sjögren's syndrome

R. Jonsson, A. Syvänen, L. Rönnblom, 2011, Genes and Immunity.

Loss of SDHB Induces a Metabolic Switch in the hPheo1 Cell Line toward Enhanced OXPHOS

P. Söderkvist, O. Gimm, C. Skoglund, 2022, International journal of molecular sciences.

Mutations in Lung Cancer Associated with Residential Radon Exposure 1

J. Lundeberg, G. Pershagen, P. Söderkvist, 1999 .

Induction of cytochrome P-450 related metabolic activities in the rat ventral prostate.

J. Gustafsson, P. Söderkvist, J. Gustafsson, 1982, Toxicology letters.

Carcinogen-binding proteins in the rat ventral prostate: specific and nonspecific high-affinity binding sites for benzo(a)pyrene, 3-methylcholanthrene, and 2,3,7,8-tetrachlorodibenzo-p-dioxin.

J. Gustafsson, L. Poellinger, P. Söderkvist, 1986, Cancer research.

Involvement of the prostatic steroid-binding protein in the transfer of ligand to the dioxin receptor.

L. Poellinger, P. Söderkvist, 1987, Carcinogenesis.

Nlrp3-inflammasome activation in non-myeloid-derived cells aggravates diabetic nephropathy

K. Reymann, T. Madhusudhan, B. Isermann, 2014, Kidney international.

Strong association between glucocerebrosidase mutations and Parkinson's disease in Sweden

P. Svenningsson, L. Forsgren, K. Wirdefeldt, 2016, Neurobiology of Aging.

Frequent allelic losses on chromosome 13q in human male breast carcinomas.

M. Gentile, S. Wingren, K. Olsen, 1997, European journal of cancer.

Expression of mRNA for Phospholipase A2, Cyclooxygenases, and Lipoxygenases in Cultured Human Umbilical Vascular Endothelial and Smooth Muscle Cells and in Biopsies from Umbilical Arteries and Veins

E. Uhl, P. Söderkvist, A. Sirsjö, 1998, Journal of Vascular Research.

Polymorphisms of GSTT1, GSTM1, and EPHX genotypes in patients with cryptogenic polyneuropathy: a case–control study

M. Tondel, M. Fredrikson, P. Söderkvist, 2011, Brain and behavior.

Uptake and specific binding of 2,3,7,8-tetrachlorodibenzo-p-dioxin in the olfactory mucosa of mice and rats.

J. Gustafsson, P. Söderkvist, E. Brittebo, 1987, Cancer research.

Interaction between smoking and glutathione S-transferase polymorphisms in solvent-induced chronic toxic encephalopathy

P. Söderkvist, U. Flodin, P. Jönsson, 2002, Toxicology and industrial health.

Liver cells contain constitutive DNase I-hypersensitive sites at the xenobiotic response elements 1 and 2 (XRE1 and -2) of the rat cytochrome P-450IA1 gene and a constitutive, nuclear XRE-binding factor that is distinct from the dioxin receptor

R. Tukey, L. Poellinger, P. Söderkvist, 1991, Molecular and cellular biology.

Glutathione S-transferase M1 null genotype as a risk modifier for solvent-induced chronic toxic encephalopathy.

O. Axelson, P. Söderkvist, U. Flodin, 1996, Scandinavian journal of work, environment & health.

Single-isomer R-salbutamol is not superior to racemate regarding protection for bronchial hyperresponsiveness.

P. Söderkvist, B. Schmekel, Anette Davidsson, 2004, Respiratory medicine.

The receptor for 2,3,7,8-TCDD: Structure, possible functions and relationship to endocrine receptors - an overview

J. Gustafsson, L. Poellinger, P. Söderkvist, 1986 .

K-ras mutations in colorectal adenocarcinomas and neighbouring transitional mucosa.

H. Zhang, P. Söderkvist, X. Sun, 1998, European journal of cancer.

Different induction mechanisms of mRNA for inducible nitric oxide synthase in rat smooth muscle cells in culture and in aortic strips

P. Söderkvist, T. Sundqvist, A. Gidlöf, 1994, FEBS letters.

Differential expression of the cytochrome P-450c and P-450d genes in the rat ventral prostate and liver.

J. Gustafsson, L. Poellinger, P. Söderkvist, 1988, Cancer research.

TP53 mutations and MDM2SNP309 identify subgroups of AML patients with impaired outcome

P. Söderkvist, H. Nahi, H. Gréen, 2015, European journal of haematology.

Formation of 8-hydroxydeoxyguanosine by asbestos and man made mineral fibres.

O. Axelson, P. Söderkvist, P. Leanderson, 1988, British journal of industrial medicine.

Genetic variation in the inflammasome and atopic dermatitis susceptibility.

P. Söderkvist, M. Winge, M. Bradley, 2013, The Journal of investigative dermatology.

Increased uptake of non‐pathogenic E. coli via the follicle‐associated epithelium in longstanding ileal Crohn's disease

P. Söderkvist, K. Magnusson, Å. Keita, 2008, The Journal of pathology.

Linköping University Post Print CARD 8 p . C 10 X polymorphism is associated with inflammatory activity in early rheumatoid arthritis

P. Söderkvist, Solbritt Rantapãã-Dahlqvist, A. Kastbom, 2010 .

CARD8 p.C10X polymorphism is associated with inflammatory activity in early rheumatoid arthritis

S. Rantapää-Dahlqvist, P. Söderkvist, A. Kastbom, 2009, Annals of the rheumatic diseases.

Gene expression of cyclooxygenase-2, group II and cytosolic phospholipase A2 in human colorectal cancer.

P. Söderkvist, J. Dimberg, A. Hugander, 1998, Anticancer research.

A TLR4 polymorphism is associated with asthma and reduced lipopolysaccharide-induced interleukin-12(p70) responses in Swedish children.

P. Söderkvist, O. Vaarala, X. Mai, 2004, The Journal of allergy and clinical immunology.

Identification and functional characterization of a novel susceptibility locus for small vessel vasculitis with MPO-ANCA

K. Lindblad-Toh, R. Jonsson, Diana Ekman, 2021, Rheumatology.

Methylation associated with long- or short-term survival in glioblastoma patients from the Nordic phase 3 trial

P. Söderkvist, J. Das, A. Malmström, 2022, Frontiers in Genetics.

Genetic deletion of mPGES-1 accelerates intestinal tumorigenesis in APC(Min/+) mice.

S. Akira, P. Söderkvist, S. Uematsu, 2008, Biochemical and biophysical research communications.

Fcγ-receptor polymorphisms associated with clinical symptoms in patients with immunoglobulin G subclass deficiency

Å. Nilsdotter-Augustinsson, P. Söderkvist, C. Dahle, 2018, Infectious diseases.

Notch1 is a frequent mutational target in chemically induced lymphoma in mouse

J. French, P. Söderkvist, Anneli Karlsson, 2008, International journal of cancer.

Glucocerebrosidase variant T369M is not a risk factor for Parkinson’s disease in Sweden

P. Svenningsson, K. Wirdefeldt, P. Söderkvist, 2022, Neuroscience Letters.

Clinical Characterization of the Pheochromocytoma and Paraganglioma Susceptibility Genes SDHA, TMEM127, MAX, and SDHAF2 for Gene-Informed Prevention

C. Larsson, C. Eng, P. Söderkvist, 2017, JAMA oncology.

Association of a protective paraoxonase 1 (PON1) polymorphism in Parkinson's disease

P. Söderkvist, M. Anvret, N. Dizdar, 2012, Neuroscience Letters.

Assessment of genetic and non-genetic risk factors for venous thromboembolism in glioblastoma - The predictive significance of B blood group.

Abdimajid Osman, P. Söderkvist, S. Uppugunduri, 2019, Thrombosis research.

The Q705K Polymorphism in NLRP3 Is a Gain-of-Function Alteration Leading to Excessive Interleukin-1β and IL-18 Production

M. Fredrikson, P. Söderkvist, J. Jönsson, 2012, PloS one.

Urinary excretion of total cystine and the dibasic amino acids arginine, lysine and ornithine in relation to genetic findings in patients with cystinuria treated with sulfhydryl compounds

H. Tiselius, P. Söderkvist, J. Jeppsson, 2003, Urological Research.

Mutation analysis of SLC7A9 in cystinuria patients in Sweden.

P. Söderkvist, T. Denneberg, E. Fjellstedt, 2003, Genetic testing.

Identification of 12 novel mutations in the SLC3A1 gene in Swedish cystinuria patients

H. Tiselius, P. Söderkvist, T. Denneberg, 2001, Human mutation.

University of Birmingham MDM2 promotor polymorphism and disease characteristics in chronic lymphocytic leukemia

R. Greil, E. Montserrat, H. Döhner, 2014 .

SLC7A9 cDNA cloning and mutational analysis of SLC3A1 and SLC7A9 in canine cystinuria

P. Söderkvist, A. Hoppe, L. Harnevik, 2006, Mammalian Genome.

Pharmacogenetics during standardised initiation of thiopurine treatment in inflammatory bowel disease

P. Söderkvist, C. Peterson, H. Hjortswang, 2006, Gut.

Group I phospholipase A2 mRNA expression in rat glandular stomach and pancreas. Ontogenic development and effects of cortisone acetate.

P. Söderkvist, C. Tagesson, B. Weström, 1992, Biochimica et biophysica acta.

MDM2 SNP309 promoter polymorphism and p53 mutations in urinary bladder carcinoma stage T1

P. Söderkvist, H. Olsson, S. Jahnson, 2013, BMC Urology.

Real-time RT-PCR methodology for quantification of thiopurine methyltransferase gene expression

P. Söderkvist, C. Peterson, S. Almér, 2003, European Journal of Clinical Pharmacology.

In response [2]

P. Söderkvist, H. Gréen, C. Peterson, 2006 .

Novel plakophilin2 mutation: Three-generation family with arrhythmogenic right ventricular cardiomyopathy

J. Engvall, P. Söderkvist, E. Nylander, 2012, Scandinavian cardiovascular journal : SCJ.

Association of Insulin-Like Growth Factor-1 Receptor Polymorphism in Dementia

J. Marcusson, P. Söderkvist, W. Sutcliffe, 2006, Dementia and Geriatric Cognitive Disorders.

Multiple sclerosis and exposure to organic solvents, investigated by genetic polymorphisms of the GSTM1 and CYP2D6 enzyme systems

P. Söderkvist, A. Landtblom, A. Ahmadi, 2003, Neurological Sciences.

Mutation analysis of the human homologue of drosophila patched and the xeroderma pigmentosum complementation group A genes in squamous cell carcinomas of the skin

P. Söderkvist, M. Ståhle-Bäckdahl, A. Undén, 1998, Molecular carcinogenesis.

Adjusted Conditioning for Allogeneic Transplantation in a Single Center Setting: Mixed Chimerism Heralds Relapse

G. Juliusson, P. Söderkvist, K. Karlsson, 2003, Leukemia & lymphoma.

Comprehensive study of thiopurine methyltransferase genotype, phenotype, and genotype-phenotype discrepancies in Sweden.

P. Söderkvist, M. L. Appell, L. Mårtensson, 2019, Biochemical pharmacology.

Matrix metalloproteinase (MMP) -1, -2, -3 and -9 promoter polymorphisms in colorectal cancer.

K. Fransén, P. Söderkvist, N. Elander, 2006, Anticancer research.

Characterization of p53 mutations in methylene chloride-induced lung tumors from B6C3F1 mice.

M. Hegi, R. Maronpot, P. Söderkvist, 1993, Carcinogenesis.

Allelotyping of butadiene-induced lung and mammary adenocarcinomas of B6C3F1 mice: frequent losses of heterozygosity in regions homologous to human tumor-suppressor genes.

E. Lander, W. Dietrich, P. Söderkvist, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Regional mapping of suppressor loci for anchorage independence and tumorigenicity on human chromosome 9.

P. Söderkvist, M. Q. Islam, L. Eklund, 2001, Cancer genetics and cytogenetics.

Telomerase reverse transcriptase mutation and the p53 pathway in T1 urinary bladder cancer

P. Söderkvist, H. Olsson, F. Aljabery, 2022 .

Association between adenomatosis polyposis coli functional status and microsomal prostaglandin E synthase‐1 expression in colorectal cancer

P. Söderkvist, Jianlin Zhou, N. Elander, 2009, Molecular carcinogenesis.

Human Gene Variants Linked to Enhanced NLRP3 Activity Limit Intramacrophage Growth of Mycobacterium tuberculosis

P. Söderkvist, Daniel Eklund, E. Särndahl, 2013, The Journal of infectious diseases.

A high frequency of sequence alterations is due to formalin fixation of archival specimens.

F. Pontén, M. Uhlén, J. Lundeberg, 1999, The American journal of pathology.

ABCB1 G1199A polymorphism and ovarian cancer response to paclitaxel.

P. Söderkvist, H. Gréen, C. Peterson, 2008, Journal of pharmaceutical sciences.

Autosomal recessive congenital hereditary corneal dystrophy associated with a novel SLC4A11 mutation in two consanguineous Tunisian families

P. Söderkvist, J. Feki, Zohra Chibani, 2021, British Journal of Ophthalmology.

Inflammasome polymorphisms confer susceptibility to sporadic malignant melanoma

M. Fredrikson, P. Söderkvist, C. Enerbäck, 2012, Pigment cell & melanoma research.

Metabolic activation of promutagens, detectable in Ames' Salmonella assay, by 5000 X g supernatant of rat ventral prostate.

J. Gustafsson, P. Söderkvist, L. Busk, 1983, Chemico-biological interactions.

Coffee, Genetic Variants, and Parkinson's Disease: Gene-Environment Interactions.

P. Söderkvist, N. Yamada-Fowler, 2015, Journal of caffeine research.

Detection of frequent allelic loss on proximal chromosome 17q in sporadic breast carcinoma using microsatellite length polymorphisms.

J. Barrett, P. Söderkvist, J. Iglehart, 1992, Cancer research.

TERT promoter mutations and polymorphisms as prognostic factors in primary glioblastoma

M. Stenmark-Askmalm, P. Söderkvist, Mohamed Ali Mosrati, 2015, Oncotarget.

Genetic and clinical basis for two distinct subtypes of primary Sjögren’s syndrome

A. Morris, K. Lindblad-Toh, R. Jonsson, 2020, Rheumatology.

Rare germline mutations identified by targeted next-generation sequencing of susceptibility genes in pheochromocytoma and paraganglioma.

Jenny Welander, Adam Andreasson, C. Larsson, 2014, The Journal of clinical endocrinology and metabolism.

Mutation analysis of the BRAF, ARAF and RAF-1 genes in human colorectal adenocarcinomas.

K. Fransén, P. Söderkvist, H. Monstein, 2003, Carcinogenesis.

Expression of cytosolic and group X secretory phospholipase A(2) genes in human colorectal adenocarcinomas.

K. Fransén, P. Söderkvist, J. Dimberg, 2002, Cancer letters.

Association of Protective HLA-A With HLA-B∗27 Positive Ankylosing Spondylitis

Mats E. Pettersson, Lina Hultin Rosenberg, K. Lindblad-Toh, 2021, Frontiers in Genetics.

Do we really know who has an MGMT methylated glioma? Results of an international survey regarding use of MGMT analyses for glioma

Bjarne Winther Kristensen, R. Henriksson, B. Kristensen, 2019, Neuro-oncology practice.

Combined Polymorphisms in Genes Encoding the Inflammasome Components NALP3 and CARD8 Confer Susceptibility to Crohn's Disease in Swedish Men

M. Fredrikson, P. Söderkvist, J. Söderholm, 2009, The American Journal of Gastroenterology.

Alterations of INPP4B, PIK3CA and pAkt of the PI3K pathway are associated with squamous cell carcinoma of the lung

P. Söderkvist, Christina Karlsson, M. Karlsson, 2014, Cancer medicine.

Genetic support for the role of the NLRP3 inflammasome in psoriasis susceptibility

P. Söderkvist, C. Enerbäck, S. Petersson, 2012, Experimental dermatology.

A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1

M. Khairallah, P. Söderkvist, A. Rebaï, 2009, Human Genetics.

Molecular identification of Helicobacter DNA present in human colorectal adenocarcinomas by 16S rDNA PCR amplification and pyrosequencing analysis.

K. Fransén, P. Söderkvist, H. Monstein, 2005, Journal of medical microbiology.

YAP1 is a potential biomarker for cetuximab resistance in head and neck cancer.

P. Söderkvist, R. Grafström, F. Jerhammar, 2014, Oral oncology.

MDM2 promotor polymorphism and disease characteristics in chronic lymphocytic leukemia: results of an individual patient data-based meta-analysis

R. Greil, E. Montserrat, H. Döhner, 2014, Haematologica.

Point mutations and deletions in the znfn1a1/ikaros gene in chemically induced murine lymphomas.

P. Söderkvist, S. Zhuang, Anneli Karlsson, 2002, Cancer research.

Genetic alterations of p53 and ras genes in 1,3-butadiene- and 2',3'-dideoxycytidine-induced lymphomas.

P. Söderkvist, T. Goodrow, C. Cochran, 1997, Cancer research.

Allelotype analysis of 2',3'-dideoxycytidine- and 1,3-butadiene-induced lymphomas in B6C3F1 mice.

P. Söderkvist, C. Cochran, S. Zhuang, 1996, Cancer research.

Genetic variation and alterations of genes involved in NFκB/TNFAIP3- and NLRP3-inflammasome signaling affect susceptibility and outcome of colorectal cancer.

M. Fredrikson, K. Fransén, P. Söderkvist, 2012, Carcinogenesis.

Environmental risk factors for Parkinson’s disease and parkinsonism: the Geoparkinson study

N. Scott, G. Prescott, C. Counsell, 2007, Occupational and Environmental Medicine.

Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison’s disease in Sweden

K. Lindblad-Toh, P. Dahlqvist, L. Rönnblom, 2018, Scientific Reports.

The NF1 gene: a frequent mutational target in sporadic pheochromocytomas and beyond.

P. Söderkvist, O. Gimm, J. Welander, 2013, Endocrine-related cancer.

Genetics and clinical characteristics of hereditary pheochromocytomas and paragangliomas.

P. Söderkvist, O. Gimm, J. Welander, 2011, Endocrine-related cancer.

Inactivations of p16INK4a-α, p16INK4a-β and p15INK4b genes in 2′, 3′-dideoxycytidine- and 1,3-butadiene-induced murine lymphomas

P. Söderkvist, A. Haugen-Strano, S. Zhuang, 1998, Oncogene.

Prognostic value of O‐6‐methylguanine–DNA methyltransferase (MGMT) protein expression in glioblastoma excluding nontumour cells from the analysis

R. Henriksson, S. Hansen, B. Kristensen, 2018, Neuropathology and applied neurobiology.

NOTCH 1 mutations influence survival in chronic lymphocytic leukemia patients

M. Fredrikson, G. Juliusson, P. Söderkvist, 2013 .

NOTCH1 mutations influence survival in chronic lymphocytic leukemia patients

M. Fredrikson, G. Juliusson, P. Söderkvist, 2013, BMC Cancer.

MDM2 SNP309 promoter polymorphism, an independent prognostic factor in chronic lymphocytic leukemia

M. Fredrikson, P. Söderkvist, J. Ungerbäck, 2010, European journal of haematology.

Extended exome sequencing identifies BACH2 as a novel major risk locus for Addison's disease

K. Lindblad-Toh, P. Dahlqvist, L. Rönnblom, 2016, Journal of internal medicine.

G/A polymorphism in intronic sequence affects the processing of MAO‐B gene in patients with Parkinson disease

P. Söderkvist, E. Jakubauskienė, A. Kanopka, 2012, FEBS letters.

Posterior microphthalmia and nanophthalmia in Tunisia caused by a founder c.1059_1066insC mutation of the PRSS56 gene.

P. Söderkvist, L. Largueche, L. Matri, 2013, Gene.

Case report: Two sisters with a germline CHEK2 variant and distinct endocrine neoplasias

J. Bishop, P. Söderkvist, A. Alli, 2022, Frontiers in Endocrinology.

Frequent EPAS1 / HIF2 a exons 9 and 12 mutations in non-familial pheochromocytoma

C. Larsson, M. Bäckdahl, P. Söderkvist, 2014 .

Molecular Profiling of Pheochromocytoma and Abdominal Paraganglioma Stratified by the PASS Algorithm Reveals Chromogranin B as Associated With Histologic Prediction of Malignant Behavior

C. Larsson, P. Söderkvist, A. Stenman, 2019, The American journal of surgical pathology.

Genetic Alterations in Mitochondrial DNA Are Complementary to Nuclear DNA Mutations in Pheochromocytomas

P. Söderkvist, L. Brunaud, M. Turkina, 2022, Cancers.

Activating FGFR1 Mutations in Sporadic Pheochromocytomas

P. Söderkvist, L. Brunaud, M. Brauckhoff, 2017, World Journal of Surgery.

Whole‐exome sequencing defines the mutational landscape of pheochromocytoma and identifies KMT2D as a recurrently mutated gene

Jenny Welander, Gerald Goh, Stefano Caramuta, 2015, Genes, chromosomes & cancer.

Role of SDHAF2 and SDHD in von Hippel–Lindau Associated Pheochromocytomas

C. Larsson, M. Bäckdahl, A. Fassina, 2014, World Journal of Surgery.

mdr-1 SNPs in Ovarian Cancer Tissue - G2677T/A Correlates with Response to Paclitaxel Chemotherapy

P. Söderkvist, H. Gréen, C. Peterson, 2010 .

mdr-1 Single Nucleotide Polymorphisms in Ovarian Cancer Tissue: G2677T/A Correlates with Response to Paclitaxel Chemotherapy

P. Söderkvist, H. Gréen, C. Peterson, 2006, Clinical Cancer Research.

Postprint Exploring the two-gene ratio in breast cancer – independent roles for HOXB 13 and IL 17 BR in prediction of clinical outcome

M. Fernö, S. Gruvberger-Saal, S. Wingren, 2008 .

Exploring the two-gene ratio in breast cancer—independent roles for HOXB13 and IL17BR in prediction of clinical outcome

M. Fernö, S. Gruvberger-Saal, S. Wingren, 2007, Breast Cancer Research and Treatment.

S100B polymorphisms are associated with age of onset of Parkinson’s disease

L. Bäckman, P. Söderkvist, A. Zettergren, 2018, BMC Medical Genetics.

Germline SDHA mutation detected by next-generation sequencing in a young index patient with large paraganglioma.

P. Söderkvist, R. Wiseman, L. Isaksson, 2013, The Journal of clinical endocrinology and metabolism.

Gene polymorphisms in the NALP3 inflammasome are associated with interleukin-1 production and severe inflammation: relation to common inflammatory diseases?

P. Söderkvist, E. Särndahl, M. Lerm, 2008, Arthritis and rheumatism.

Identification of two novel sequence variants affecting thiopurine methyltransferase enzyme activity.

P. Söderkvist, C. Peterson, E. Lyrenäs, 2004, Pharmacogenetics.

Explaining TPMT genotype/phenotype discrepancy by haplotyping of TPMT*3A and identification of a novel sequence variant, TPMT*23

P. Söderkvist, C. Peterson, K. Skoglund, 2007, Pharmacogenetics and genomics.

No Induction of Thiopurine Methyltransferase During Thiopurine Treatment in Inflammatory Bowel Disease

P. Söderkvist, C. Peterson, H. Hjortswang, 2006, Nucleosides, nucleotides & nucleic acids.

pheochromocytomas and paragangliomas

P. Söderkvist, O. Gimm, J. Welander, 2011 .

p53 mutations in larynx cancer.

K. Hemminki, P. Söderkvist, W. Szyfter, 1994, Carcinogenesis.

Androgen receptor and vitamin D receptor gene polymorphisms and prostate cancer risk.

P. Söderkvist, E. Varenhorst, P. Andersson, 2006, European journal of cancer.

PROX1 is a novel pathway-specific prognostic biomarker for high-grade astrocytomas; results from independent glioblastoma cohorts stratified by age and IDH mutation status

R. Stupp, F. Pontén, R. Henriksson, 2016, Oncotarget.

P03.15 Detection of 1p19q co-deletion in oligodendrogliomas with droplet digital PCR.

P. Söderkvist, A. Malmström, M. Hallbeck, 2017 .

Association of breast cancer progression with a vitamin D receptor gene polymorphism. South-East Sweden Breast Cancer Group.

S. Wingren, P. Söderkvist, A. Lundin, 1999, Cancer research.

Deletions on Chromosome Y and Downregulation of the SRY Gene in Tumor Tissue Are Associated with Worse Survival of Glioblastoma Patients

P. Söderkvist, A. Smits, A. Dimberg, 2021, Cancers.

Absence of hot spot mutations of the PIK3CA gene in acute myeloid leukaemia

P. Söderkvist, J. Jönsson, P. Andersson, 2006, European journal of haematology.

Mutations in the isocitrate dehydrogenase 2 gene and IDH1 SNP 105C > T have a prognostic value in acute myeloid leukemia

P. Söderkvist, E. Paul, M. Hermansson, 2014, Biomarker Research.

Sex Disparities in MGMT Promoter Methylation and Survival in Glioblastoma: Further Evidence from Clinical Cohorts

P. Söderkvist, A. Smits, A. Malmström, 2021, Journal of clinical medicine.

ABCB1 single-nucleotide variants and survival in patients with glioblastoma treated with radiotherapy concomitant with temozolomide

M. Stenmark-Askmalm, P. Söderkvist, H. Gréen, 2019, The Pharmacogenomics Journal.

Postoperative neoadjuvant temozolomide before radiotherapy versus standard radiotherapy in patients 60 years or younger with anaplastic astrocytoma or glioblastoma: a randomized trial

R. Henriksson, S. Hansen, G. Stragliotto, 2017, Acta oncologica.

Mycobacterium tuberculosis

P. Söderkvist, Daniel Eklund, E. Särndahl, 2004, Kafka.

Novel BEST1 gene mutations associated with two different forms of macular dystrophy in Tunisian families

P. Söderkvist, M. Hmani-Aifa, Annette Molbaek, 2019, Clinical & experimental ophthalmology.

X-chromosome variants are associated with aldosterone producing adenomas

T. Arnesen, P. Söderkvist, M. Larsson, 2021, Scientific Reports.

Proton pump inhibitors for Barrett's oesophagus

G. Crosthwaite, P. Söderkvist, P. Gionchetti, 2000, Gut.

Genetic variation in proteins of the cryopyrin inflammasome influences susceptibility and severity of rheumatoid arthritis (the Swedish TIRA project).

P. Söderkvist, G. Wingren, T. Skogh, 2007, Rheumatology.

Genetic variants in CARD8 but not in NLRP3 are associated with ankylosing spondylitis

P. Söderkvist, A. Kastbom, H. Forsblad-d’Elia, 2013, Scandinavian journal of rheumatology.

Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family

W. Kimberling, S. Riazuddin, P. Söderkvist, 2009, European Journal of Human Genetics.

Association between ulcerative growth and hypoxia inducible factor‐1α polymorphisms in colorectal cancer patients

M. Fredrikson, M. Fenech, K. Fransén, 2006, Molecular carcinogenesis.

Allele frequency spectrum of known ankylosing spondylitis associated variants in a Swedish population

K. Lindblad-Toh, P. Söderkvist, A. Kastbom, 2021, Scandinavian journal of rheumatology.

Implementing precision medicine in a regionally organized healthcare system in Sweden

L. Levin, D. Gisselsson, T. Fioretos, 2022, Nature Medicine.

The 158V polymorphism of Fc gamma receptor type IIIA in early rheumatoid arthritis: increased susceptibility and severity in male patients (the Swedish TIRA project).

P. Söderkvist, T. Skogh, A. Kastbom, 2005, Rheumatology.

GSTM1 and mEPHX polymorphisms in Parkinson's disease and age of onset.

O. Axelson, M. Fredrikson, P. Söderkvist, 2000, Biochemical and biophysical research communications.

Abstract 1041: Alterations of INPP4B, PIK3CA and pAkt of the PI3K pathway are associated with squamous cell carcinoma of the lung

P. Söderkvist, Christina Karlsson, M. Karlsson, 2011 .

Absence of the BRAF V600E mutation in pheochromocytoma

P. Söderkvist, C. Juhlin, A. Stenman, 2016, Journal of Endocrinological Investigation.

Mercury toxicokinetics--dependency on strain and gender.

P. Söderkvist, J. Nielsen, Rudolfs K. Zalups, 2010, Toxicology and applied pharmacology.

Fcγ receptor type IIIA genotype and response to tumor necrosis factor α-blocking agents in patients with rheumatoid arthritis

Thomas Skogh, L. Padyukov, P. Söderkvist, 2007 .

Structure and function of the dioxin receptor: A DNA-binding protein similar to steroid hormone receptors

J. Gustafsson, L. Poellinger, P. Söderkvist, 1987 .

Genetic associations of Nrf2-encoding NFE2L2 variants with Parkinson’s disease – a multicenter study

H. Zetterberg, A. Quattrone, O. Hammarsten, 2014, BMC Medical Genetics.

The relationship between blood flow, development of edema and leukocyte accumulation in post-ischemic rat skeletal muscle.

P. Söderkvist, G. Nylander, D. Lewis, 1990, Microcirculation, endothelium, and lymphatics.

Single Nucleotide Polymorphisms in MORC4, CD14, and TLR4 Are Related to Outcome of Allogeneic Stem Cell Transplantation.

P. Söderkvist, E. Norén, K. Lotfi, 2016, Annals of transplantation.

Determination of dimethylhippuric acid isomers in urine by high-performance liquid chromatography

P. Söderkvist, J. Järnberg, D. Lindmark, 1996, International archives of occupational and environmental health.

Ontogeny of group II phospholipase A2 gene expression in rat stomach and ileum.

P. Söderkvist, C. Tagesson, I. Lilja, 1995, Biology of the neonate.

β-Tubulin mutations in ovarian cancer using single strand conformation analysis-risk of false positive results from paraffin embedded tissues

P. Söderkvist, H. Gréen, C. Peterson, 2006 .

Case report: A somatic mutation in CLCN2 identified in a sporadic aldosterone producing adenoma.

T. Arnesen, P. Söderkvist, M. Walz, 2019, European journal of endocrinology.

Characteristics of Disease and Some Exposure Considerations

O. Axelson, P. Söderkvist, 1991 .

A Patient with a Phenotype of Adult-onset Still Disease, But a Genotype Typical of Cryopyrin-associated Periodic Fever Syndrome

P. Söderkvist, C. Jacobs, P. Eriksson, 2013, The Journal of Rheumatology.

Two adult siblings with atypical cryopyrin-associated periodic syndrome due to a novel M299V mutation in NLRP3.

P. Söderkvist, M. Ejdebäck, E. Särndahl, 2010, Arthritis and rheumatism.

Polymorphisms in CARD8 and NLRP3 are associated with extrapulmonary TB and poor clinical outcome in active TB in Ethiopia

M. Fredrikson, P. Söderkvist, M. Lerm, 2019, Scientific Reports.

A pilot study on risk factors and p53 gene expression in colorectal cancer.

O. Axelson, M. Fredrikson, P. Söderkvist, 1996, British Journal of Cancer.

Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and mice

Richard S. Smith, P. Söderkvist, G. Howell, 2011, Nature Genetics.

Print β-tubulin mutations in ovarian cancer using single strand conformation analysis – risk of false positive results from paraffin embedded tissues

P. Söderkvist, H. Gréen, G. Horvath, 2010 .

Association between inflammasome-related polymorphisms and psoriatic arthritis

S. Rantapää-Dahlqvist, P. Söderkvist, A. Kastbom, 2020, Scandinavian journal of rheumatology.

Variation in the fat mass and obesity‐related (FTO) genotype is not associated with body fatness in infants, but possibly with their length

E. Forsum, P. Söderkvist, M. Löf, 2014, Pediatric obesity.

Caffeine Interaction with Glutamate Receptor Gene GRIN2A: Parkinson's Disease in Swedish Population

M. Fredrikson, P. Söderkvist, N. Yamada-Fowler, 2014, PloS one.

Analysis of VEGF polymorphisms, tumor expression of VEGF mRNA and colorectal cancer susceptibility in a Swedish population.

P. Söderkvist, N. Elander, J. Ungerbäck, 2009, Molecular medicine reports.

On the Use of Molecular Biology Data in Occupational and Environmental Epidemiology

P. Söderkvist, Olav Axelson, 1995, Journal of occupational and environmental medicine.

Complementary somatic mutations of KCNJ5, ATP1A1, and ATP2B3 in sporadic aldosterone producing adrenal adenomas.

T. Arnesen, P. Söderkvist, M. Brauckhoff, 2014, Endocrine-related cancer.

Complementary somatic mutations of KCNJ5, ATP1A1, and ATP2B3 in sporadic aldosterone producing adrenal adenomas.

T. Arnesen, P. Söderkvist, M. Brauckhoff, 2014, Endocrine-related cancer.

Differential expression of cyclooxygenase 2 in human colorectal cancer

P. Söderkvist, J. Dimberg, A. Hugander, 1999, Gut.

Nitric oxide synthase 2 mRNA expression in relation to p53 and adenomatous polyposis coli mutations in primary colorectal adenocarcinomas.

K. Fransén, P. Söderkvist, A. Sirsjö, 2002, Surgery.

Frequent mutations of the Trp53, Hras1 and β-catenin (Catnb) genes in 1,3-butadiene-induced mammary adenocarcinomas in B6C3F1 mice

P. Söderkvist, S. Zhuang, R. Wiseman, 2002, Oncogene.

Nitric oxide synthase 2 (NOS2) promoter polymorphisms in colorectal cancer.

K. Fransén, P. Söderkvist, N. Elander, 2005, Cancer letters.

BRCA1 mutations in primary breast and ovarian carcinomas.

M. Skolnick, D. Ballinger, A. Berchuck, 1994, Science.

pheochromocytomas and paragangliomas

P. Söderkvist, O. Gimm, J. Welander, 2011 .

Telomerase reverse transcriptase mutation and the p53 pathway in T1 urinary bladder cancer

P. Söderkvist, H. Olsson, F. Aljabery, 2021, BJU International.

Bank1 and NF-kappaB as key regulators in anti-nucleolar antibody development

P. Söderkvist, J. Nielsen, P. Hultman, 2018, PloS one.

Syddansk Universitet Bank 1 and NF-kappaB as key regulators in anti-nucleolar antibody development

P. Söderkvist, J. Nielsen, P. Hultman, 2018 .

Nuclear and mitochondrial DNA alterations in pheochromocytomas and paragangliomas and their potential treatment.

P. Söderkvist, O. Gimm, Mouna Tabebi, 2022, Endocrine-Related Cancer.

Extended exome sequencing identifies BACH2 as a novel major risk locus for Addison's disease

K. Lindblad-Toh, P. Dahlqvist, L. Rönnblom, 2016, Journal of internal medicine.

Polymorphisms in NALP3 inflammasome components NLRP3 and CARD8 affect C-peptide secretion in type 1 diabetes

M. Fredrikson, P. Söderkvist, R. Casas, 2013 .

TERT promoter mutations and polymorphisms as prognostic factors in primary glioblastoma

M. Stenmark-Askmalm, P. Söderkvist, Mohamed Ali Mosrati, 2015, Oncotarget.

MDM2 SNP309 promoter polymorphism, an independent prognostic factor in chronic lymphocytic leukemia

M. Fredrikson, P. Söderkvist, J. Ungerbäck, 2010, European journal of haematology.

Genetics and clinical characteristics of hereditary pheochromocytomas and paragangliomas.

P. Söderkvist, O. Gimm, J. Welander, 2011, Endocrine-related cancer.

Domain landscapes of somatic NF1 mutations in pheochromocytoma and paraganglioma.

P. Söderkvist, F. Frikha, O. Gimm, 2023, Gene.

Complementary somatic mutations of KCNJ5, ATP1A1, and ATP2B3 in sporadic aldosterone producing adrenal adenomas.

T. Arnesen, P. Söderkvist, M. Brauckhoff, 2014, Endocrine-related cancer.

Genetics of primary hyperaldosteronism.

P. Söderkvist, O. Gimm, Ravi Kumar Dutta, 2016, Endocrine-related cancer.