K. Hussein

H. Kreipe, K. Hussein, J. Lemound, 2016, Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology.

Thrombospondin-1 (TSP-1) in primary myelofibrosis (PMF) — a megakaryocyte-derived biomarker which largely discriminates PMF from essential thrombocythemia

N. Kröger, H. Kreipe, G. Büsche, 2010, Annals of Hematology.

Identification of new target molecules PTK2, TGFBR2 and CD9 overexpressed during advanced bone marrow remodelling in primary myelofibrosis

N. Kröger, H. Kreipe, G. Büsche, 2009, British journal of haematology.

Myelofibrosis in Philadelphia chromosome-negative myeloproliferative neoplasms is associated with aberrant karyotypes.

H. Kreipe, D. Jonigk, K. Hussein, 2013, Cancer genetics.

Clinically latent and autopsy-verified inflammatory disorders and malignant tumours in transplant patients

H. Kreipe, K. Hussein, J. Salem, 2020, Journal of Clinical Pathology.

Aberrant expression of caspase 14 in salivary gland carcinomas.

N. Gellrich, H. Kreipe, M. Stoetzer, 2015, Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology.

Expression of Caspase 14 and Filaggrin in Oral Squamous Carcinoma

H. Kreipe, A. Eckardt, K. Hussein, 2013, Head and Neck Pathology.

Expression profiling of apoptosis-related genes in megakaryocytes: BNIP3 is downregulated in primary myelofibrosis.

H. Kreipe, K. Hussein, K. Theophile, 2008, Experimental hematology.

Systemic mastocytosis (SM) with associated BCR-ABL-positive myelogenous leukaemia (SM-AHNMD): evidence that mast cells do not belong to the leukaemic clone

M. Görner, H. Kreipe, G. Büsche, 2011, Leukemia.

Myelofibrosis evolving during imatinib treatment of a chronic myeloproliferative disease with coexisting BCR-ABL translocation and JAK2V617F mutation.

H. Kreipe, M. Flasshove, K. Hussein, 2007, Blood.

CD133 marks a stem cell population that drives human primary myelofibrosis

N. Kröger, B. Fehse, C. Stocking, 2013, Haematologica.

Clinical utility gene card for: familial polycythaemia vera

H. Kreipe, O. Shpilberg, K. Hussein, 2012, European Journal of Human Genetics.

Different lineage involvement in myelodysplastic/myeloproliferative disease with combined MPLW515L and JAK2V617F mutation

H. Kreipe, K. Hussein, K. Theophile, 2009, British journal of haematology.

NEW RECORD OF GIANT DEVIL RAY (CHONDRICHTHYES: MYLIOBATIDAE) FROM ORAN BAY (WESTERN MEDITERRANEAN SEA)

K. Hussein, Lotfi Bensahla Talet, 2019, Indonesian Fisheries Research Journal.

Tumour angiogenesis in Epstein-Barr virus-associated post-transplant smooth muscle tumours

H. Kreipe, D. Jonigk, K. Hussein, 2014, Clinical Sarcoma Research.

Malignancies after pediatric kidney transplantation: more than PTLD?

B. Maecker-Kolhoff, H. Kreipe, M. Mynarek, 2014, Pediatric Nephrology.

Profile of fibrosis-related gene transcripts and megakaryocytic changes in the bone marrow of myelodysplastic syndromes with fibrosis

H. Kreipe, K. Hussein, A. Stucki-Koch, 2018, Annals of Hematology.

Expression of adhesion factor CD239 in bone marrow cells in chronic myeloproliferative diseases

H. Kreipe, K. Hussein, K. Theophile, 2009, Journal of Thrombosis and Thrombolysis.

Opposite expression pattern of Src kinase Lyn in acute and chronic haematological malignancies

H. Kreipe, G. Büsche, K. Hussein, 2009, Annals of Hematology.

Obliterative airway remodelling in transplanted and non-transplanted lungs

T. Welte, F. Laenger, U. Lehmann, 2010, Virchows Archiv.

Epstein-Barr Virus-Associated Smooth Muscle Tumours after Transplantation, Infection with Human Immunodeficiency Virus and Congenital Immunodeficiency Syndromes

F. Donnerstag, F. Laenger, B. Maecker-Kolhoff, 2013, Pathobiology.

Molecular and Clinicopathological Analysis of Epstein‐Barr Virus–Associated Posttransplant Smooth Muscle Tumors

C. Klein, F. Laenger, B. Maecker-Kolhoff, 2012, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Post-transplant Lymphoproliferative Disease

B. Maecker-Kolhoff, S. Gottschalk, K. Hussein, 2021, Pediatric Liver Transplantation.

Posttransplant Lymphoproliferative Disorder in Pediatric Patients

B. Maecker-Kolhoff, H. Kreipe, K. Hussein, 2013, Pathobiology.

Risk Factors and Prognosis in T-Cell Posttransplantation Lymphoproliferative Diseases: Reevaluation of 163 Cases

C. Klein, B. Maecker-Kolhoff, H. Kreipe, 2013, Transplantation.

"Hypoxia-induced down-regulation of microRNA-449a/b impairs control over targeted SERPINE1 (PAI-1) mRNA - a mechanism involved in SERPINE1 (PAI-1) overexpression"

H. Kreipe, K. Hussein, K. Theophile, 2010, Journal of translational medicine.

Complement receptor-associated CD163+/CD18+/CD11c+/CD206-/CD209- expression profile in chronic histiocytic intervillositis of the placenta.

H. Kreipe, K. Hussein, Annette M. Müller, 2019, Placenta.

Hepatic and Adrenocortical Choristomas in the Placenta

K. Hussein, Nora Schaumann, 2020, Fetal and pediatric pathology.

Molecular defects in BRAF wild-type ameloblastomas and craniopharyngiomas—differences in mutation profiles in epithelial-derived oropharyngeal neoplasms

C. Hartmann, U. Lehmann, H. Kreipe, 2018, Virchows Archiv.

Clinico-pathological characteristics of different types of immunodeficiency-associated smooth muscle tumours.

H. Kreipe, D. Jonigk, K. Hussein, 2014, European journal of cancer.

Meta-analysis of teeth from European populations before and after the 18th century reveals a shift towards increased prevalence of caries and tooth loss.

K. Hussein, Antonia Müller, 2017, Archives of oral biology.

Paleopathology of the juvenile Pharaoh Tutankhamun—90th anniversary of discovery

A. Nerlich, K. Hussein, E. Matin, 2013, Virchows Archiv.

Comparison of clinical diagnoses and autopsy findings in 54 cases with lymphoid neoplasms

H. Kreipe, K. Hussein, L. Abraham, 2019, Journal of Hematopathology.

New concepts of personalized therapy in salivary gland carcinomas.

A. Quaas, V. Grünwald, K. Hussein, 2017, Oral oncology.

MicroRNA expression profiling of megakaryocytes in primary myelofibrosis and essential thrombocythemia

B. Wiese, H. Kreipe, K. Hussein, 2009, Platelets.

Non-canonical WNT6/WNT10A signal factor expression in EBV+ post-transplant smooth muscle tumors

F. Laenger, H. Kreipe, D. Jonigk, 2018, Clinical Sarcoma Research.

Undifferentiated embryonal sarcoma of the liver in adults

P. Lenz, H. Kreipe, W. Domschke, 2008, Cancer.

Significant inverse correlation of microRNA-150/MYB and microRNA-222/p27 in myelodysplastic syndrome.

H. Kreipe, B. Schlegelberger, G. Büsche, 2010, Leukemia research.

Partial Hydatidiform Mole With Extensive Angiomatoid Vessel Configuration in a First Trimester Miscarriage

A. Caliebe, K. Hussein, J. Oates, 2015, International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists.

Array-CGH and quantitative PCR genetic analysis in a case with bilateral hypoplasia of pulmonary arteries and lungs and simultaneous unilateral renal agenesis.

D. Steinemann, H. Scholz, H. Kreipe, 2010, International journal of clinical and experimental pathology.

Expression analysis of leukocytes attracting cytokines in chronic histiocytic intervillositis of the placenta.

H. Kreipe, K. Hussein, C. von Kaisenberg, 2013, International journal of clinical and experimental pathology.

Insights into JAK2-V617F mutation in CML.

H. Kreipe, G. Büsche, K. Hussein, 2007, The Lancet. Oncology.

Increased megakaryocytic proliferation, pro-platelet deposition and expression of fibrosis-associated factors in children with chronic myeloid leukaemia with bone marrow fibrosis

H. Kreipe, K. Hussein, G. Göhring, 2017, Leukemia.

Villitis of unknown etiology and chronic deciduitis are not associated with human papilloma virus and enterovirus infection

A. Heim, K. Hussein, T. Hager, 2020, Virchows Archiv.

Post‐transplant lymphoproliferative disorders with naso‐ and oropharyngeal manifestation

B. Maecker-Kolhoff, H. Kreipe, K. Hussein, 2015, Transplant international : official journal of the European Society for Organ Transplantation.

A Review on the Occurrence of the Blunthead Puffer, Sphoeroides pachygaster (Müller & Troschel, 1848) in the Mediterranean with a New Occurrence from Oran Bay (Western Algeria)

K. Hussein, Lotfi Bensahla Talet, Amine Chakouri, 2021 .

Problems and pitfalls in grading of bone marrow fibrosis, collagen deposition and osteosclerosis – a consensus‐based study

H. Stein, M. Werner, S. Dirnhofer, 2016, Histopathology.

EBV-Specific T-Cell Immunity in Pediatric Solid Organ Graft Recipients With Posttransplantation Lymphoproliferative Disease

W. Klapper, C. Klein, T. Schulz, 2013, Transplantation.

Clinical utility gene card for: familial erythrocytosis

M. McMullin, M. Percy, K. Hussein, 2012, European Journal of Human Genetics.

Familial polycythemia vera with non-germ line JAK2V617F mutation sparing the abnormal and clonal granulopoiesis

D. Steinemann, M. Ballmaier, U. Lehmann, 2007, Leukemia.

Erythrocytosis in children and adolescents—classification, characterization, and consensus recommendations for the diagnostic approach

S. Hermouet, H. Cario, D. Pospíšilová, 2013, Pediatric blood & cancer.

Circulating Cytokine Levels as Markers of Inflammation in Philadelphia Negative Myeloproliferative Neoplasms: Diagnostic and Prognostic Interest

K. Hussein, P. Mossuz, J. Mondet, 2015, Mediators of inflammation.

Myelofibrosis: molecular and cell biological aspects

H. Kreipe, G. Büsche, K. Hussein, 2012, Fibrogenesis & tissue repair.

Biclonal expansion and heterogeneous lineage involvement in a case of chronic myeloproliferative disease with concurrent MPLW515L/JAK2V617F mutation.

M. Ballmaier, N. Kröger, H. Kreipe, 2009, Blood.

B‐CLL developing in a patient with PV is not affected by V617F mutation of the Janus kinase 2

M. Ballmaier, H. Kreipe, K. Hussein, 2006, European journal of haematology.

Gene expression profiling in laser-microdissected bone marrow megakaryocytes.

K. Hussein, 2011, Methods in molecular biology.

Massive Perivillous Fibrin Deposition of an Enterovirus A-Infected Placenta Associated With Stillbirth: A Case Report

A. Heim, K. Hussein, H. Feist, 2018, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Cytokine Expression Pattern in Bone Marrow Microenvironment after Allogeneic Stem Cell Transplantation in Primary Myelofibrosis.

N. Kröger, H. Kreipe, K. Hussein, 2016, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

primary myelofibrosis SRSF2 mutation is present in the hypercellular and prefibrotic stage of

R. Geffers, U. Lehmann, H. Kreipe, 2013 .

MPLW515L mutation in acute megakaryoblastic leukaemia

A. Porwit, D. Jonigk, K. Hussein, 2009, Leukemia.

Hypoxia-induced down-regulation of microRNA-449a/b impairs control over targeted SERPINE1 (PAI-1) mRNA - a mechanism involved in SERPINE1 (PAI-1) overexpression

H. Kreipe, K. Hussein, O. Bock, 2010, Journal of Translational Medicine.

Erratum to Hypoxia-induced down-regulation of microRNA-449a/b impairs control over targeted SERPINE1 (PAI-1) mRNA - a mechanism involved in SERPINE1 (PAI-1) overexpression

H. Kreipe, K. Hussein, O. Bock, 2009, Journal of Translational Medicine.

Characteristics of Early and Late PTLD Development in Pediatric Solid Organ Transplant Recipients

A. Großhennig, C. Klein, T. Schulz, 2013, Transplantation.

IDH mutation analysis is not suitable for the routine molecular diagnostic algorithm in myeloproliferative and myelodysplastic neoplasms.

H. Kreipe, K. Hussein, O. Bock, 2010, Blood.

Organizing pneumonia in mice and men

F. Laenger, A. Haverich, D. Jonigk, 2016, Journal of Translational Medicine.

Chronic myeloproliferative diseases with concurrent BCR–ABL junction and JAK2V617F mutation

G. Büsche, K. Hussein, K. Theophile, 2008, Leukemia.

SRSF2 mutation is present in the hypercellular and prefibrotic stage of primary myelofibrosis.

R. Geffers, U. Lehmann, H. Kreipe, 2013, Blood.

Useful Tool for the Routine Diagnostic Algorithm in Chronic Stage Ph Ϫ Mpn and Mds

H. Kreipe, K. Hussein, Bianca M. Engelhardt, 2010 .

Meta-analysis on COVID-19-pregnancy-related placental pathologies shows no specific pattern

K. Hussein, Nora Schaumann, J-T Suhren, 2021, Placenta.

Megakaryocytic expression of miRNA 10a, 17-5p, 20a and 126 in Philadelphia chromosome-negative myeloproliferative neoplasm

H. Kreipe, K. Hussein, K. Theophile, 2009, Annals of Hematology.

Pathoanatomical Lesions in Placentas With Excessively Hypercoiled Umbilical Cords: Frequent Detection of Massive Perivillous Fibrin Deposition

K. Hussein, J. Wohlschlaeger, H. Feist, 2020, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Expression of Toll-Like Receptors in Chronic Histiocytic Intervillositis of the Placenta

H. Kreipe, K. Hussein, A. Stucki-Koch, 2015, Fetal and pediatric pathology.

The suppressor of cytokine signalling-1 (SOCS-1) gene is overexpressed in Philadelphia chromosome negative chronic myeloproliferative disorders.

B. Wiese, H. Kreipe, K. Hussein, 2007, Leukemia research.

MicroRNA expression profiles in BCR-ABL-negative primary myelofibrosis with chromosome 7q defects

H. Kreipe, K. Hussein, A. Stucki-Koch, 2015, Journal of Hematopathology.

PHAGOCYTES , GRANULOCYTES , AND MYELOPOIESIS A lack of secretory leukocyte protease inhibitor ( SLPI ) causes defects in granulocytic differentiation

K. Welte, K. Hussein, J. Skokowa, 2014 .

Discordancy for Placental Massive Perivillous Fibrin Deposition and Fetal Growth in Dichorionic Twins after in Vitro Fertilization

G. Rau, K. Hussein, H. Feist, 2015, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Hypoxia Induces Mesenchymal Gene Expression in Renal Tubular Epithelial Cells: An in vitro Model of Kidney Transplant Fibrosis

H. Kreipe, J. Becker, R. Schmitt, 2013, Nephron Extra.

Ovarectomy despite Negative Imaging in Anti-NMDA Receptor Encephalitis: Effective Even Late

C. Trebst, K. Hussein, M. Stangel, 2013, Case reports in neurological medicine.

CXCL13 as a Novel Marker for Diagnosis and Disease Monitoring in Pediatric PTLD

C. Klein, L. Pape, H. Haller, 2012, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

MicroRNA expression in Epstein-Barr virus-associated post-transplant smooth muscle tumours is related to leiomyomatous phenotype

F. Laenger, B. Maecker-Kolhoff, H. Kreipe, 2013, Clinical Sarcoma Research.

Expression of myelopoiesis-associated microRNA in bone marrow cells of atypical chronic myeloid leukaemia and chronic myelomonocytic leukaemia

H. Kreipe, G. Büsche, K. Hussein, 2011, Annals of Hematology.

Molecular profile of inflammatory and megakaryocytic factors in pediatric myelodysplastic syndrome with acute myelofibrosis

I. Baumann, C. Niemeyer, H. Kreipe, 2018, Pediatric blood & cancer.

CD20/CD79a/PAX5/CD3-negative post-transplant lymphoma with aberrant actin and desmin co-expression—a potential differential diagnostic pitfall between PTLD and PTSMT

H. Kreipe, K. Hussein, J. Schlué, 2022, Annals of Hematology.

Comparison of Prenatal and Postmortem Diagnoses from 251 Fetal Autopsies: High Rate of Placenta Pathologies, Low Rate of Discrepancies

K. Hussein, H. Kreipe, Nora Schaumann, 2023, Fetal and pediatric pathology.

A human immunodeficiency syndrome caused by mutations in CARMIL2

J. Puchalka, C. Klein, C. Walz, 2017, Nature Communications.