U. Kristoffersson

发表

Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization.

N. Carter, C. Gillberg, E. Blennow, 1995, American journal of medical genetics.

Disease associated balanced chromosome rearrangements: a resource for large scale genotype-phenotype delineation in man

Kim R. Rasmussen, C. Lundsteen, N. Tommerup, 2000, Journal of medical genetics.

A century of Hereditas: from local publication to international journal

Fredrik Åström, U. Kristoffersson, Anna Tunlid, 2020, Hereditas.

Developing a framework for implementation of genetic services: learning from examples of testing for monogenic forms of common diseases

J. Broerse, M. Cornel, T. Rigter, 2014, Journal of Community Genetics.

Increased Cancer Risk in Families with Pediatric Cancer Is Associated with Gender, Age, Diagnosis, and Degree of Relation to the Child

M. Stenmark-Askmalm, I. Øra, H. Olsson, 2020, Cancer Epidemiology, Biomarkers & Prevention.

Increased incidence of childhood, prostate and breast cancers in relatives of childhood cancer patients

H. Jernström, H. Olsson, T. Wiebe, 2012, Familial Cancer.

Provision of genetic services in Europe: current practices and issues

B. Godard, S. Aymé, L. Tranebjaerg, 2003, European Journal of Human Genetics.

Nephrosis and disturbances of neuronal migration in male siblings--a new hereditary disorder?

I. Hägerstrand, A. Brun, U. Kristoffersson, 1986, Archives of disease in childhood.

Variant Ph translocations in chronic myeloid leukemia.

F. Mitelman, N. Mandahl, S. Heim, 1985, Cancer genetics and cytogenetics.

Testing the children: do non-genetic health-care providers differ in their decision to advise genetic presymptomatic testing on minors? A cross-sectional study in five countries in the European Union.

J. Schmidtke, M. Cornel, Hillary Harris, 2009, Genetic testing and molecular biomarkers.

Frequency of RET mutations in long‐ and short‐segment Hirschsprung disease

B. Pasini, M. Abramowicz, D. Cass, 1997, Human mutation.

Population‐based cohort investigations of the risk for malignant tumors in first‐degree relatives and wives of men with breast cancer

H. Olsson, T. Möller, O. Johansson, 1993, Cancer.

Reciprocal translocation t(3;12)(q27;q13) in lipoma.

F. Mitelman, A. Rydholm, N. Mandahl, 1986, Cancer genetics and cytogenetics.

Multiple structural chromosome rearrangements, including del(7q) and del(10q), in an adenocarcinoma of the prostate.

F. Mitelman, N. Mandahl, S. Heim, 1988, Cancer genetics and cytogenetics.

Report of an International Survey of Molecular Genetic Testing Laboratories

M. Somerville, D. Barton, D. Taruscio, 2007, Public Health Genomics.

Karyotypic patterns in chronic myeloproliferative disorders: report on 74 cases and review of the literature.

F. Mitelman, F. Mertens, S. Heim, 1991, Leukemia.

Genetics in clinical practice: general practitioners' educational priorities in European countries

C. Julian‐Reynier, J. Schmidtke, H. Harris, 2008, Genetics in Medicine.

Regulatory Issues for Genetic Testing in Clinical Practice

U. Kristoffersson, 2008, Molecular biotechnology.

Regulation of genetic testing in clinical practice.

U. Kristoffersson, 2004, Methods in molecular medicine.

Double minutes in two primary adenocarcinomas of the prostate.

F. Mitelman, N. Mandahl, J. Limon, 1989, Cancer genetics and cytogenetics.

Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas.

C. Larsson, B. Teh, J. Cardinal, 1996, The Journal of clinical endocrinology and metabolism.

Have patients ’ opinion been asked ? A review of 102 studies from the years 1997 – 2007 on patient perspective of genetic counselling services in genetic testing situations

J. Schmidtke, U. Kristoffersson, H. Kääriäinen, 2008 .

Health needs assessment for medical genetic services for congenital disorders in middle- and low-income nations

A. Kent, J. Schmidtke, R. Zimmern, 2013, Journal of Community Genetics.

High resolution analysis of the 5q-marker chromosome in refractory anemia.

F. Mitelman, G. Manolov, Y. Manolova, 2008, Hereditas.

Clinical Course of Early Onset Prostate Cancer with Special Reference to Family History as a Prognostic Factor

H. Olsson, O. Bratt, U. Kristoffersson, 1998, European Urology.

Higher occurrence of childhood cancer in families with germline mutations in BRCA2, MMR and CDKN2A genes

Å. Borg, M. Nilbert, H. Olsson, 2008, Familial Cancer.

High resolution chromosome analysis of constitutional and acquired t(15;17) maps c-erbA to subband 17q11.2.

F. Mitelman, G. Manolov, Y. Manolova, 1986, Cancer genetics and cytogenetics.

Familial and hereditary prostate cancer in southern Sweden. A population-based case-control study.

H. Olsson, O. Bratt, U. Kristoffersson, 1999, European journal of cancer.

Community genetics. Its definition 2010

P. Rahman, Sonia S Anand, J. Schmidtke, 2010, Journal of Community Genetics.

Chromosome aberrations in prophylactic mastectomies from women belonging to breast cancer families

Å. Borg, H. Olsson, F. Mitelman, 1996 .

Mutation analysis and prenatal diagnosis in a Lesch-Nyhan family showing non-random X-inactivation interfering with carrier detection tests

U. Francke, B. Lambert, U. Kristoffersson, 1992, Human Genetics.

Monosomy and trisomy of 15q24→qter in a family with a translocation t(6;15)(P25;q24)

N. Mandahl, S. Heim, I. Hägerstrand, 1987, Clinical genetics.

Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: Prevalence and characterization by fluorescence in situ hybridization

E. Blennow, G. Annéren, M. Nordenskjöld, 1994, Prenatal diagnosis.

Prevalence of Stroke and Vascular Risk Factors among First-Degree Relatives of Stroke Patients and Control Subjects

B. Norrving, A. Lindgren, H. Luthman, 2005, Cerebrovascular Diseases.

Assessing educational priorities in genetics for general practitioners and specialists in five countries: factor structure of the Genetic-Educational Priorities (Gen-EP) scale

J. Schmidtke, C. Julian‐Reynier, H. Harris, 2008, Genetics in Medicine.

Structural chromosomal abnormalities of 3q in myelodysplastic syndrome/acute myeloid leukaemia with Sweet's syndrome

F. Mitelman, N. Mandahl, S. Heim, 1990, European journal of haematology.

Genetic Testing and Common Disorders: How to Assess Relevance and Possibilities

A. Cambon-Thomsen, M. Krawczak, J. Lubiński, 2011 .

ECA Permanent working group for cytogenetics and society: Cytogenetic guidelines and quality assurance. A common framework for quality assessment for constitutional and acquired cytogenetic investigations

R. Hastings, S. Cavani, F. Bricarelli, 2006 .

Genetic Screening in Europe

J. Schmidtke, J. Sequeiros, U. Kristoffersson, 2010, Public Health Genomics.

hMLH1, hMSH2 and hMSH6 mutations in hereditary non‐polyposis colorectal cancer families from Southern Sweden

Å. Borg, H. Olsson, P. Mangell, 1999, International journal of cancer.

Hypereosinophilic syndrome in a child mosaic for a congenital triplication of the short arm of chromosome 8

A. Egesten, S. Garwicz, U. Kristoffersson, 1997, British journal of haematology.

The risk of malignant tumours in first-degree relatives of men with early onset prostate cancer: a population-based cohort study.

H. Olsson, O. Bratt, U. Kristoffersson, 1997, European journal of cancer.

Telomeric association in a malignant fibrous histiocytoma

F. Mitelman, A. Rydholm, N. Mandahl, 2004, Human Genetics.

Structural chromosome aberrations in a case of angioleiomyoma.

F. Mitelman, A. Rydholm, N. Mandahl, 1986, Cancer genetics and cytogenetics.

Long-term prognosis of early-onset breast cancer in a population-based cohort with a known BRCA1/2 mutation status

N. Loman, O. Johannsson, L. Hartman, 2014, Breast Cancer Research and Treatment.

Updated Stroke Gene Panels: Rapid evolution of knowledge on monogenic causes of stroke

F. de Leeuw, A. Lindgren, J. Putaala, 2022, European Journal of Human Genetics.

Increased frequency of chromosome aberrations in long-term cultured cerebrospinal fluid lymphocytes of patients with multiple sclerosis

M. Sandberg‐Wollheim, N. Mandahl, B. Högstedt, 1991, Journal of the Neurological Sciences.

Heterogeneity and Low Detection Rate of RET Mutations in Hirschsprung Disease

B. Pasini, B. Hamel, M. Abramowicz, 1994, European journal of human genetics : EJHG.

Regulations and practices of genetic counselling in 38 European countries: the perspective of national representatives

J. Schmidtke, J. Sequeiros, U. Kristoffersson, 2008, European Journal of Human Genetics.

Editorial: Genetics and Democracy

M. Hedlund, Niclas Hagen, U. Kristoffersson, 2012, Journal of Community Genetics.

Cytogenetic Guidelines and Quality Assurance: a common European framework for quality assessment for constitutional and acquired cytogenetic investigations

P. Patsalis, R. Hastings, S. Cavani, 2007, European Journal of Human Genetics.

Deletion of 14q in non‐Hodgkin's lymphoma

H. Olsson, F. Mitelman, N. Mandahl, 1990, European journal of haematology.

What's new in lymphoma cytogenetics?

U. Kristoffersson, 1988, Pathology, research and practice.

Relationship between cytogenetic findings and histopathology in non-Hodgkin lymphoma.

H. Olsson, F. Mitelman, S. Heim, 2009, Acta pathologica, microbiologica, et immunologica Scandinavica. Section A, Pathology.

Contribution to the 18q‐ syndrome. A patient with del (18) (q22.3qter)

H. Sjöström, O. Norén, U. Kristoffersson, 1987, Clinical genetics.

Cytogenetic studies in non-Hodgkin lymphomas--results from surgical biopsies.

H. Olsson, F. Mitelman, S. Heim, 2008, Hereditas.

Cytogenetic studies of childhood non-Hodgkin lymphomas.

F. Mitelman, S. Heim, S. Garwicz, 2008, Hereditas.

Fine needle aspiration biopsy: a useful tool in tumor cytogenetics with special reference to malignant lymphomas.

H. Olsson, F. Mitelman, U. Kristoffersson, 1981, Cancer genetics and cytogenetics.

Marker ring chromosome--a new cytogenetic abnormality characterizing lipogenic tumors?

F. Mitelman, A. Rydholm, N. Mandahl, 1987, Cancer genetics and cytogenetics.

No abnormal C-band polymorphism in lung cancer patients.

H. Olsson, F. Mitelman, R. Berger, 2008, Hereditas.

Constitutional C-band polymorphism in lymphocytes from patients with chronic myeloid leukemia.

F. Mitelman, R. Berger, A. Bernheim, 2008, Hereditas.

C-band polymorphism in non-Hodgkin lymphoma.

H. Olsson, F. Mitelman, R. Berger, 2008, Hereditas.

C-band heteromorphism in breast cancer patients.

H. Olsson, F. Mitelman, R. Berger, 1985, Cancer genetics and cytogenetics.

Differences in human C-band pattern between two European populations.

F. Mitelman, R. Berger, A. Bernheim, 2008, Hereditas.

Multiple clonal chromosome aberrations in two thymomas.

F. Mitelman, N. Mandahl, S. Heim, 1989, Cancer genetics and cytogenetics.

Normal frequency of structural chromosome aberrations in fibroblasts from patients with non-Hodgkin's lymphoma.

H. Olsson, F. Mitelman, F. Mertens, 2008, Hereditas.

BRCAsearch: written pre-test information and BRCA1/2 germline mutation testing in unselected patients with newly diagnosed breast cancer

Å. Borg, N. Loman, T. Törngren, 2017, Breast Cancer Research and Treatment.

Trisomy 14 in atypical chronic myeloid leukemia.

D. Catovsky, F. Mertens, N. Mandahl, 1990, Leukemia.

Relation between occupational exposure to organic solvents and chromosome aberrations in non‐Hodgkin's lymphoma

F. Mitelman, H. Olsson, L. Brandt, 1989, European journal of haematology.

Cytogenetic studies in non-Hodgkin lymphomas--results from fine-needle aspiration samples.

H. Olsson, F. Mitelman, M. Åkerman, 2008, Hereditas.

Quality Issues in Clinical Genetic Services

J. Cassiman, J. Schmidtke, U. Kristoffersson, 2010, Springer Netherlands.

Genetics and democracy—what is the issue?

Niclas Hagen, Susanne Lundin, Shai Mulinari, 2013, Journal of Community Genetics.

Tetraploid karyotype (92,XXYY) in two patients with acute lymphoblastic leukemia.

F. Mitelman, N. Mandahl, S. Heim, 1987, Cancer genetics and cytogenetics.

Trisomy 7, trisomy 10, and loss of the Y chromosome in short-term cultures of normal kidney tissue.

J. Cigudosa, F. Mitelman, N. Mandahl, 1990, Cytogenetics and cell genetics.

Piebaldism in a Mentally Retarded Girl With Rare Deletion of the Long Arm of Chromosome 4

R. Ljung, U. Kristoffersson, R. Sijmons, 1993, Pediatric dermatology.

Ring Y chromosome in an azoospermic male with short stature: additional evidence for a distinct ring Y syndrome in non‐mosaic patients?

D. Gisselsson, A. Giwercman, U. Kristoffersson, 2003, Clinical genetics.

Identification of human candidate genes for male infertility by digital differential display.

N. Tommerup, E. van Assche, C. Hansen, 2001, Molecular human reproduction.

An improved technique for short-term culturing of human prostatic adenocarcinoma tissue for cytogenetic analysis.

F. Mitelman, N. Mandahl, J. Limon, 1990, Cancer genetics and cytogenetics.

Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study

V. Pankratz, F. Couch, B. Bonanni, 2012, British Journal of Cancer.

Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers

J. S. Hoffman, W. Chung, V. Pankratz, 2012, Human mutation.

An excess of chromosome 1 breakpoints in male infertility

R. Stallings, C. Lundsteen, Z. Tümer, 2004, European Journal of Human Genetics.

Pseudohypoparathyroidism type I and Albright's hereditary osteodystrophy with a proximal 15q chromosomal deletion in mother and daughter

K. Berntorp, U. Kristoffersson, K. Arheden, 1992, Clinical genetics.

External quality assessment for mutation detection in the BRCA1 and BRCA2 genes: EMQN's experience of 3 years.

D. Stoppa-Lyonnet, U. Kristoffersson, C. Mueller, 2004, Annals of oncology : official journal of the European Society for Medical Oncology.

Characterization of add(I)(p36) in non‐hodgkin lymphomas by fluorescence in situ hybridization

P. Pisa, M. Nordenskjöld, K. Brøndum‐Nielsen, 1995 .

Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer.

Å. Borg, N. Loman, O. Johannsson, 1997, American journal of human genetics.

Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers

Peter Devilee, Alfons Meindl, Lesley McGuffog, 2010, Breast Cancer Research.

Deletion of chromosome arm 3p in hematologic malignancies

B. Johansson, F. Mitelman, S. Garwicz, 1997, Leukemia.

Bone marrow karyotypes in 94 children with acute leukemia

F. Mitelman, N. Mandahl, S. Heim, 1990, European journal of haematology.

Association Between BRCA1 and BRCA2 Mutations and Survival in Women With Invasive Epithelial Ovarian Cancer

Gord Glendon, Lesley McGuffog, Daniel Barrowdale, 2012 .

Functional analysis of BRCA1 C-terminal missense mutations identified in breast and ovarian cancer families.

P. Møller, Å. Borg, N. Loman, 2001, Human molecular genetics.

Constitutive heterochromatin C-band polymorphism in prostatic cancer.

R. Berger, U. Kristoffersson, R. Lundgren, 1991, Cancer Genetics and Cytogenetics.

Prognostic implications of cytogenetic aberrations in diffuse large B‐cell lymphomas

B. Johansson, F. Mitelman, M. Jerkeman, 1999, European journal of haematology.

Prognostic implication of cytogenetic findings in 106 patients with non-Hodgkin lymphoma.

J. Ranstam, H. Olsson, F. Mitelman, 1987, Cancer genetics and cytogenetics.

Breakprone chromosome bands in fibroblasts from patients with non-Hodgkin's lymphoma do not coincide with bands involved in primary rearrangements in non-Hodgkin's lymphomas.

H. Olsson, F. Mitelman, F. Mertens, 2008, Hereditas.

One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations: results of a prospective study in Southern Sweden.

Å. Borg, N. Loman, H. Olsson, 2004, European journal of cancer.

Prevalence of germline TP53 mutations and history of Li–Fraumeni syndrome in families with childhood adrenocortical tumors, choroid plexus tumors, and rhabdomyosarcoma: A population‐based survey

D. Gisselsson, Å. Borg, H. Olsson, 2012, Pediatric blood & cancer.

Biparental inheritance of chromosomal abnormalities in male twins with non-syndromic mental retardation.

Z. Tümer, N. Tommerup, Y. Mang, 2011, European journal of medical genetics.

Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities

A. Janssens, A. Cambon-Thomsen, M. Krawczak, 2011, European Journal of Human Genetics.

Background Document to the ESHG recommendations on genetic testing and common disorders

A. Cambon-Thomsen, M. Krawczak, J. Lubiński, 2011 .

New structural chromosomal rearrangements in congenital leukemia.

F. Mitelman, N. Mandahl, S. Heim, 1987, Leukemia.

Family history of breast and ovarian cancers and BRCA1 and BRCA2 mutations in a population-based series of early-onset breast cancer.

Å. Borg, N. Loman, O. Johannsson, 2001, Journal of the National Cancer Institute.

Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke

Sofie Samuelsson, Arne Lindgren, Ulf Kristoffersson, 2020, Stroke.

HRPT2, encoding parafibromin, is mutated in hyperparathyroidism–jaw tumor syndrome

J. Carpten, E. Gillanders, J. Trent, 2002, Nature Genetics.

A squamous cell bladder carcinoma with karyotypic abnormalities reminiscent of transitional cell carcinoma.

F. Mitelman, N. Mandahl, S. Heim, 1989, The Journal of urology.

Late appearing 5q--marker in refractory anemia.

F. Mitelman, N. Mandahl, S. Heim, 1987, Cancer genetics and cytogenetics.

High resolution banding analysis of the reciprocal translocation t(6;9) in acute nonlymphocytic leukemia.

F. Mitelman, N. Mandahl, S. Heim, 1986, Cancer genetics and cytogenetics.

CD30‐positive large cell lymphomas (‘Ki‐1 lymphoma’) are associated with a chromosomal translocation involving 5q35

R. Warnke, H. Tilly, C. Bastard, 1990, British journal of haematology.

A child with interstitial deletion of chromosome No. 5.

U. Kristoffersson, I. Felding, 2009, Hereditas.

Identification, characterisation and clinical applications of cosmids from the telomeric and centromeric regions of the long arm of chromosome 22

E. Blennow, J. Dumanski, M. Nordenskjöld, 1994, Human Genetics.

A new specific chromosomal rearrangement, t(8;16) (p11;p13), in acute monocytic leukaemia

F. Mitelman, N. Mandahl, S. Heim, 1987, British journal of haematology.

The action of hexyl mercury bromide on CHinese hamster cells in vitro.

U. Kristoffersson, 2009, Annales de cardiologie et d'angeiologie.

Partial trisomy 15(q25qter) in two brothers.

U. Kristoffersson, B. Bergwall, 2008, Hereditas.

Tandem duplication (1) (q11 → q22) in a male infant with multiple congenital malformations

F. Mertens, M. Forslund, U. Kristoffersson, 1987, Clinical genetics.

Duplication 18p with mild influence on the phenotype.

F. Mertens, B. Johansson, U. Kristoffersson, 1988, American journal of medical genetics.

Normal high-resolution karyotypes in three patients with the Holt-Oram syndrome.

F. Mitelman, N. Mandahl, S. Heim, 1987, American journal of medical genetics.

Educational priorities and current involvement in genetic practice: a survey of midwives in the Netherlands, UK and Sweden.

C. Julian‐Reynier, J. Schmidtke, H. Harris, 2009, Midwifery.

Reflecting on Earlier Experiences with Unsolicited Findings: Points to Consider for Next-Generation Sequencing and Informed Consent in Diagnostics

Q. Waisfisz, M. Cornel, P. Borry, 2013, Human mutation.

Targeted sequencing of BRCA1 and BRCA2 across a large unselected breast cancer cohort suggests that one-third of mutations are somatic

L. Saal, Å. Borg, N. Loman, 2016, Annals of oncology : official journal of the European Society for Medical Oncology.

A Nonsynonymous Polymorphism in IRS1 Modifies Risk of Developing Breast and Ovarian Cancers in BRCA1 and Ovarian Cancer in BRCA2 Mutation Carriers

W. Chung, V. Pankratz, F. Couch, 2012, Cancer Epidemiology, Biomarkers & Prevention.

Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers.

F. Couch, B. Karlan, J. Benítez, 2011, Journal of the National Cancer Institute.

A common European framework for quality assessment for constitutional, acquired and molecular cytogenetic investigations. E.C.A. Permanent Working Group for Cytogenetics and Society

R. Hastings, R. Howell, S. Cavani, 2012 .

Association of the Variants CASP8 D302H and CASP10 V410I with Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

F. Couch, T. Rebbeck, J. Benítez, 2010, Cancer Epidemiology, Biomarkers & Prevention.

Hemizygosity for chromosome 2q14.2‐q22.1 spanning the GLI2 and PROC genes associated with growth hormone deficiency, polydactyly, deep vein thrombosis and urogenital abnormalities

Å. Borg, G. Jönsson, J. Staaf, 2006, Clinical genetics.

Cytogenetics of secondary myelodysplasia (sMDS) and acute nonlymphocvtic leukemia (sANLL)

F. Mertens, S. Heim, B. Johansson, 1991, European journal of haematology.

Segregation analysis of balanced pericentric inversions in pedigree data

N. Morton, J. Lindsten, M. Petersen, 1986, Clinical Genetics.

Clinical and immunohistochemical findings in a case of neonatal Marfan syndrome

I. Hägerstrand, K. Hanséus, G. Björkhem, 1995, Acta paediatrica.

Prevalence of germline pathogenic variants in 22 cancer susceptibility genes in Swedish pediatric cancer patients

J. Koster, M. Stenmark-Askmalm, I. Øra, 2021, Scientific Reports.

Chromosome aberrations in prophylactic mastectomies from women belonging to breast cancer families.

Å. Borg, H. Olsson, F. Mitelman, 1996, Genes, chromosomes & cancer.

The contribution of the hereditary nonpolyposis colorectal cancer syndrome to the development of ovarian cancer.

Å. Borg, M. Nilbert, B. Halvarsson, 2006, Gynecologic oncology.

CAG repeat length in the androgen receptor gene is related to age at diagnosis of prostate cancer and response to endocrine therapy, but not to prostate cancer risk

Å. Borg, H. Olsson, O. Bratt, 1999, British Journal of Cancer.

A new specific chromosomal rearrangement, t(11;20)(p15;q11), in myeloblastic leukemia with maturation.

F. Mitelman, N. Mandahl, S. Heim, 1988, Leukemia.

Incidence of malignant tumours in relatives of BRCA1 and BRCA2 germline mutation carriers.

Å. Borg, N. Loman, O. Johannsson, 1999, European journal of cancer.

Risk Factors of Breast Cancer in Relation to a Family History of Breast Cancer in Southern Sweden1

J. Ranstam, H. Olsson, U. Kristoffersson, 1985 .

The need for oncogenetic counselling Ten years’ experience of a regional oncogenetic clinic

H. Olsson, U. Kristoffersson, K. Henriksson, 2004, Acta oncologica.

Genetic testing in women with early-onset breast cancer: a Traceback pilot study

Carolina Ellberg, H. Ehrencrona, Hampus Olsson, 2021, Breast Cancer Research and Treatment.

Efficacy versus effectiveness of clinical genetic testing criteria for BRCA1 and BRCA2 hereditary mutations in incident breast cancer

L. Saal, N. Loman, C. Larsson, 2017, Familial Cancer.

High risk of in-breast tumor recurrence after BRCA1/2-associated breast cancer

Å. Borg, N. Loman, H. Olsson, 2014, Breast Cancer Research and Treatment.

Cytogenetic findings in acute megakaryoblastic leukemia (ANLL-M7).

P. Nilsson, F. Mitelman, F. Mertens, 1990, Cancer genetics and cytogenetics.

A methylation PCR approach for detection of fragile X syndrome

C. Lassen, P. Åman, I. Panagopoulos, 1999, Human mutation.

A novel PCR‐based approach for the detection of the Huntington disease associated trinucleotide repeat expansion

C. Lassen, P. Åman, I. Panagopoulos, 1999, Human mutation.

Bone marrow karyotype and prognosis in primary myelodysplastic syndromes

F. Mitelman, N. Mandahl, S. Heim, 1988, European journal of haematology.

First-trimester diagnosis on chorionic villi obtained by direct vision technique

F. Mitelman, B. Gustavii, U. Kristoffersson, 1984, Human Genetics.

Chromosome studies in a thymoma in vitro

U. Kristoffersson, 2004, Humangenetik.

Variant translocation t(3;15)(q21;q22) in a patient with acute promyelocytic leukemia.

F. Mitelman, N. Mandahl, S. Heim, 1988, Leukemia.

Cytogenetic studies in Hodgkin's disease.

H. Olsson, F. Mitelman, N. Mandahl, 2009, Acta pathologica, microbiologica, et immunologica Scandinavica. Section A, Pathology.

Near-haploidy in a case of plasmocytoma.

H. Olsson, F. Mitelman, D. Kelly, 1986, Cancer genetics and cytogenetics.

Trisomy 13 as a primary chromosome aberration in acute leukemia.

F. Mitelman, F. Mertens, S. Heim, 1991, Cancer genetics and cytogenetics.

What is ideal genetic counselling? A survey of current international guidelines

J. Schmidtke, J. Sequeiros, U. Kristoffersson, 2008, European Journal of Human Genetics.

Ischaemic stroke in hypertensive patients is associated with variations in the PDE4D genome region

B. Norrving, A. Lindgren, H. Luthman, 2008, European Journal of Human Genetics.

Risk perception, screening practice and interest in genetic testing among unaffected men in families with hereditary prostate cancer.

H. Grönberg, H. Olsson, J. Damber, 2000, European journal of cancer.

Germline mutations in BRCA1 and BRCA2 incidentally revealed in a biobank research study: experiences from re-contacting mutation carriers and relatives

L. Saal, Å. Borg, N. Loman, 2017, Journal of Community Genetics.

Scope of definitions of genetic testing: evidence from a EuroGentest survey

Jörg Schmidtke, Elina Rantanen, Jorge Sequeiros, 2010, Journal of Community Genetics.

Familial aggregation of stroke amongst young patients in Lund Stroke Register

M. Soller, A. Ilinca, U. Kristoffersson, 2016, European journal of neurology.

Chromosome analysis in 100 cases of first trimester trophoblast sampling

Ulf Kristoffersson, F. Mitelman, N. Mandahl, 1985, Clinical genetics.

Evidence for SMAD 3 as a modifier of breast cancer risk in BRCA 2 mutation carriers

V. Pankratz, F. Couch, T. Rebbeck, 2010 .

The FHIT and PTPRG genes are deleted in benign proliferative breast disease associated with familial breast cancer and cytogenetic rearrangements of chromosome band 3p14.

Å. Borg, F. Mitelman, F. Mertens, 1996, Cancer research.

Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness

Pascal Borry, Heidi C Howard, Jörg Schmidtke, 2014, European Journal of Human Genetics.

Trichorhinophalangeal syndrome type I: symptoms and signs, radiology and genetics.

N. Mandahl, C. Werner, L. Stigsson, 1986, Annals of the rheumatic diseases.

Clinical impact of breakpoint position within M-bcr in chronic myeloid leukemia.

F. Mitelman, T. Fioretos, P. Åman, 1993, Leukemia.

Reciprocal translocation (11;19)(q23;p13) in congenital acute lymphoblastic leukemia.

F. Mitelman, N. Mandahl, S. Heim, 1986, Cancer genetics and cytogenetics.

Sons of men with prostate cancer: their attitudes regarding possible inheritance of prostate cancer, screening, and genetic testing.

H. Olsson, O. Bratt, U Kristoffersson, 1997, Urology.

EuroGentest: DNA-Based Testing for Heritable Disorders in Europe

Jörg Schmidtke, Jorge Sequeiros, Helena Kääriäinen, 2008, Public Health Genomics.

Remarkably long survival of a patient with Ph1-positive chronic myeloid leukemia and 5' bcr rearrangement.

F. Mitelman, T. Fioretos, F. Mertens, 1990, Leukemia.

Broad phenotypic spectrum in familial adenomatous polyposis; from early onset and severe phenotypes to late onset of attenuated polyposis with the first manifestation at age 72

O. Johannsson, P. Mangell, M. Nilbert, 2008, BMC Medical Genetics.

Accuracy of self-reported family history of cancer, mutation status and tumor characteristics in patients with early onset breast cancer

Å. Borg, H. Olsson, Carolina Ellberg, 2017, Acta oncologica.

Editorial: Genetics and Democracy

M. Hedlund, U. Kristoffersson, N. Hagen, 2012, Journal of Community Genetics.

The wide variation of definitions of genetic testing in international recommendations, guidelines and reports

J. Schmidtke, J. Cassiman, J. Sequeiros, 2012, Journal of Community Genetics.

Confidence of primary care physicians in their ability to carry out basic medical genetic tasks—a European survey in five countries—Part 1

Jörg Schmidtke, Elizabeth Anionwu, Ulf Kristoffersson, 2011, Journal of Community Genetics.

Genetic education and nongenetic health professionals: Educational providers and curricula in Europe

J. Schmidtke, C. Julian‐Reynier, H. Harris, 2005, Genetics in Medicine.

A stroke gene panel for whole-exome sequencing

A. Lindgren, M. Soller, A. Ilinca, 2018, European Journal of Human Genetics.

A large-sample assessment of possible association between ischaemic stroke and rs12188950 in the PDE4D gene

O. Melander, B. Norrving, B. Hedblad, 2012, European Journal of Human Genetics.

A child with double trisomy: 48,XYY,+18.

U. Kristoffersson, I. Felding, 2009, Hereditas.

Multiple cytogenetic abnormalities in a case of osteosarcoma.

F. Mitelman, A. Rydholm, N. Mandahl, 1986, Cancer genetics and cytogenetics.

Do clonal chromosome abnormalities prognosticate early relapse in Hodgkin's disease?

H. Olsson, F. Mitelman, N. Mandahl, 1988, Cancer genetics and cytogenetics.

No correlation between hyperthermia during pregnancy and Hirschsprung disease in the offspring.

U. Kristoffersson, L. Larsson, L. Okmian, 1989, American journal of medical genetics.

Quality Guidelines and Standards for Genetic Laboratories/Clinics in Prenatal Diagnosis on Fetal Samples Obtained by Invasive Procedures

U. Kristoffersson, Eucromic Quality Assessment Group, 1997, European journal of human genetics : EJHG.

Cytogenetic diagnosis of meningeal carcinomatosis.

F. Mitelman, U. Kristoffersson, E. Dahlquist, 1980, The New England journal of medicine.

Germline mutations in BRCA1 and BRCA2 incidentally revealed in a biobank research study: experiences from re-contacting mutation carriers and relatives

L. Saal, Å. Borg, N. Loman, 2017, Journal of Community Genetics.

Genomic amplification of CCND2 is rare in non-Hodgkin lymphomas.

M. Höglund, B. Johansson, F. Mitelman, 1998, Cancer genetics and cytogenetics.

Chromosome analysis of a newly established renal carcinoma cell line.

U. Kristoffersson, R. Lundgren, Y. Jin, 1988, Cancer genetics and cytogenetics.

Novel germline APC mutations in Swedish patients with familial adenomatous polyposis and Gardner syndrome.

M. Nilbert, J. Fernebro, U. Kristoffersson, 2000, Scandinavian journal of gastroenterology.

Hypophyseal tumor and gynecomastia preceding bilateral breast cancer development in a man

M. Landin-Olsson, H. Olsson, U. Kristoffersson, 1984, Cancer.

Are 25 SNPs from the CARDIoGRAM study associated with ischaemic stroke?

O. Melander, B. Norrving, B. Hedblad, 2013, European journal of neurology.

Proliferative activity and number of clonal chromosome aberrations in non-Hodgkin's lymphomas.

H. Olsson, L. Brandt, U. Kristoffersson, 2009, Scandinavian journal of haematology.

Rare diseases: past achievements and future prospects

Victoria Hedley, U. Kristoffersson, B. Tumienė, 2021, Journal of Community Genetics.

Definitions of genetic testing in European legal documents

J. Schmidtke, J. Cassiman, J. Sequeiros, 2012, Journal of Community Genetics.

The Use of Principles in Allocating Scarce Health Care Resources for Genetic Tests

W. Rogowski, P. Carlsson, U. Kristoffersson, 2010 .

EMQN Best Practice Guidelines for Molecular Genetic Analysis in Hereditary Breast/Ovarian Cancer

Å. Borg, N. Loman, C. Lázaro, 2008 .

Association between BRCA1 and BRCA2 mutations and survival in women with invasive epithelial ovarian cancer.

Douglas F. Easton, Daniel Barrowdale, Sue Healey, 2012, JAMA.

Trisomy 5 and t(5;14)(q11;q32) as the sole abnormalities in two different clones from a centroblastic non-Hodgkin's lymphoma.

H. Olsson, F. Mitelman, N. Mandahl, 1988, Cancer genetics and cytogenetics.

Association between BRCA1 and BRCA2 mutations and survival in women with invasive epithelial ovarian cancer.

Lesley, A. Whittemore, M. García-Closas, 2012, Journal of the American Medical Association (JAMA).

The effect of cyclamate and saccharin on the chromosomes of a Chinese hamster cell line.

U. Kristoffersson, 2009, Hereditas.

From Mendel to Medical Genetics

M. Macek, U. Kristoffersson, 2017, European Journal of Human Genetics.

A stroke gene panel for whole-exome sequencing

A. Lindgren, M. Soller, A. Ilinca, 2018, European Journal of Human Genetics.