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Researcher
Lennart Raman
Profile
Projects
Publications
Activities
Awards & Distinctions
17
Results
2022
Application of an ultrasensitive NGS-based blood test for the diagnosis of early-stage lung cancer : sensitivity, a hurdle still difficult to overcome
Malaïka Van der Linden
Bram Van Gaever
Lennart Raman
Karim Vermaelen
Ingel Demedts
Veerle Surmont
Ulrike Himpe
Yolande Lievens
Liesbeth Ferdinande
Franceska Dedeurwaerdere
et al.
A1
Journal Article
in
CANCERS
2022
GENType : all-in-one preimplantation genetic testing by pedigree haplotyping and copy number profiling suitable for third-party reproduction
Lisa De Witte
Lennart Raman
Machteld Baetens
Andries De Koker
Nico Callewaert
Sofie Symoens
Kelly Tilleman
Frauke Vanden Meerschaut
Annelies Dheedene
Björn Menten
A1
Journal Article
in
HUMAN REPRODUCTION
2022
Shallow whole-genome sequencing : a useful, easy to apply molecular technique for CNA detection on FFPE tumor tissue : a glioma-driven study
Kim Van der Eecken
Malaïka Van der Linden
Lennart Raman
David Creytens
Franceska Dedeurwaerdere
Koen De Winne
Liesbeth Ferdinande
Martin Lammens
Björn Menten
Isabelle Rottiers
et al.
A1
Journal Article
in
VIRCHOWS ARCHIV
2022
Shallow-depth sequencing of cell-free DNA for Hodgkin and diffuse large B-cell lymphoma (differential) diagnosis : a standardized approach with underappreciated potential
Lennart Raman
Malaïka Van der Linden
Ciel De Vriendt
Bliede Van den Broeck
Kristoff Muylle
Dries Deeren
Franceska Dedeurwaerdere
Sofie Verbeke
Amélie Dendooven
Katrien De Grove
et al.
A1
Journal Article
in
HAEMATOLOGICA
2022
The feasibility of using liquid biopsies as a complementary assay for copy number aberration profiling in routinely collected paediatric cancer patient samples
Ruben Van Paemel
Charlotte Vandeputte
Lennart Raman
Jolien Van Thorre
Leen Willems
Jo Van Dorpe
Malaïka Van der Linden
Jilke De Wilde
Andries De Koker
Björn Menten
et al.
A1
Journal Article
in
EUROPEAN JOURNAL OF CANCER
2022
2021
Copy number and methylation profiling of cell-free DNA for tumor and prenatal diagnostics : a multi-cohort research effort
Lennart Raman
Jo Van Dorpe
Björn Menten
Dissertation
2021
Myxoid pleomorphic liposarcoma : a clinicopathologic, immunohistochemical, molecular genetic and epigenetic study of 12 cases, suggesting a possible relationship with conventional pleomorphic liposarcoma
David Creytens
Andrew L. Folpe
Christian Koelsche
Thomas Mentzel
Liesbeth Ferdinande
Joost M. van Gorp
Malaïka Van der Linden
Lennart Raman
Björn Menten
Karen Fritchie
et al.
A1
Journal Article
in
MODERN PATHOLOGY
2021
2020
Detection of copy number alterations by shallow whole-genome sequencing of formalin-fixed, paraffin-embedded tumor tissue
Malaïka Van der Linden
Lennart Raman
Ansel Vander Trappen
Annelies Dheedene
Matthias De Smet
Tom Sante
David Creytens
Yolande Lievens
Björn Menten
Jo Van Dorpe
et al.
A1
Journal Article
in
ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE
2020
Shallow whole-genome sequencing of cell-free DNA for B-cell lymphoma diagnosis and disease monitoring : a standardized approach with underappreciated potential
Malaïka Van der Linden
Lennart Raman
Ciel De Vriendt
Bliede Van den Broeck
Kristoff Muylle
Dries Deeren
Kathleen Claes
Björn Menten
Fritz Offner
Jo Van Dorpe
C3
Conference
2020
Shallow whole-genome sequencing of cell-free DNA for B-cell lymphoma diagnosis and disease monitoring: a standardized approach with underappreciated potential
Malaïka Van der Linden
Lennart Raman
Ciel De Vriendt
Bliede Van den Broeck
Kristoff Muylle
Dries Deeren
Kathleen Claes
Björn Menten
Fritz Offner
Jo Van Dorpe
C3
Conference
2020
Shallow whole-genome sequencing of plasma cell-free DNA accurately differentiates small from non-small cell lung carcinoma
Lennart Raman
Malaïka Van der Linden
Kim Van der Eecken
Karim Vermaelen
Ingel Demedts
Veerle Surmont
Ulrike Himpe
Franceska Dedeurwaerdere
Liesbeth Ferdinande
Yolande Lievens
et al.
A1
Journal Article
in
GENOME MEDICINE
2020
2019
Clinical experience with shallow whole genome sequencing as a detection method for Copy Number Variations
Björn Menten
Maarten De Smet
Lennart Raman
Tom Sante
Nadine Van Roy
Annelies Dheedene
C3
Conference
2019
Exploring the potential of shallow whole-genome sequencing for diagnosis and disease monitoring of lymphoma in liquid biopsy
Lennart Raman
Malaïka Van der Linden
Ciel De Vriendt
Bliede Van den Broeck
Kristoff Muylle
Dries Deeren
Björn Menten
Fritz Offner
Jo Van Dorpe
C3
Conference
2019
Preface : in silico pipeline for accurate cell-free fetal DNA fraction prediction
Lennart Raman
Machteld Baetens
Matthias De Smet
Annelies Dheedene
Jo Van Dorpe
Björn Menten
A1
Journal Article
in
PRENATAL DIAGNOSIS
2019
WisecondorX : improved copy number detection for routine shallow whole-genome sequencing
Lennart Raman
Annelies Dheedene
Matthias De Smet
Jo Van Dorpe
Björn Menten
A1
Journal Article
in
NUCLEIC ACIDS RESEARCH
2019
2018
Detection of copy number alterations using shallow whole genome sequencing on formalin-fixed paraffin-embedded tumor tissue
Malaïka Van der Linden
Lennart Raman
Ansel Vander Trappen
Annelies Dheedene
Matthias De Smet
Tom Sante
David Creytens
Björn Menten
Jo Van Dorpe
Nadine Van Roy
C3
Conference
2018
Detection of copy number alterations using shallow whole genome sequencing on formalin-fixed paraffin-embedded tumor tissue
Malaïka Van der Linden
Lennart Raman
Ansel Vander Trappen
Annelies Dheedene
Matthias De Smet
Tom Sante
David Creytens
Björn Menten
Jo Van Dorpe
Nadine Van Roy
C3
Conference
2018