Not finding it? Sign in to also search OpenAlex live.
-
Explainable multi-view framework for dissecting intercellular signaling from highly multiplexed spatial data2020 bioRxiv (Cold Spring Harbor Laboratory) preprint Biochemistry, Genetics and Molecular Biology Single-cell and spatial transcriptomics Open access
Jovan Tanevski, Ricardo O. Ramirez Flores, Attila Gábor, Denis Schapiro, Julio Sáez-Rodríguez
28citations -
From Mechanism-Based Retaining Glycosidase Inhibitors to Activity-Based Glycosidase Profiling2024 Journal of the American Chemical Society article Chemistry Carbohydrate Chemistry and Synthesis Open access
Marta Artola, Johannes M. F. G. Aerts, Gijsbert A. van der Marel, Carme Rovira, Jeroen D. C. Codée, G.J. Davies, +1 more
26citations -
The genome of New Zealand trevally (Carangidae: Pseudocaranx georgianus) uncovers a XY sex determination locus2021 BMC Genomics article Biochemistry, Genetics and Molecular Biology Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities Open access
Andrew S. Catanach, Mike Ruigrok, Deepa R. Bowatte, Marcus W. Davy, Roy D. Storey, Noémie Valenza-Troubat, +5 more
25citations -
Isolation and Characterization of Shewanella Phage Thanatos Infecting and Lysing Shewanella oneidensis and Promoting Nascent Biofilm Formation2020 Frontiers in Microbiology article Environmental Science Bacteriophages and microbial interactions Open access
Maximilian Kreienbaum, Anja K. Dörrich, David Brandt, Nicole E. Schmid, Tabea Leonhard, Fabian Tobias Hager, +7 more
21citations -
Medical Records-Based Genetic Studies of the Complement System2021 Journal of the American Society of Nephrology article Immunology and Microbiology Complement system in diseases Open access
Atlas Khan, Ning Shang, Lynn Petukhova, Jun Zhang, Yufeng Shen, Scott Joseph Hebbring, +15 more
16citations -
Evaluation of in silico predictors on short nucleotide variants in HBA1, HBA2, and HBB associated with haemoglobinopathies2022 eLife article Biochemistry, Genetics and Molecular Biology Genomics and Rare Diseases Open access
Stella Tamana, Maria Xenophontos, Anna Minaidou, Coralea Stephanou, Cornelis L. Harteveld, Celeste Bento, +10 more
15citations -
Systematic Minigene-Based Splicing Analysis and Tentative Clinical Classification of 52 CHEK2 Splice-Site Variants2023 Clinical Chemistry article Biochemistry, Genetics and Molecular Biology BRCA gene mutations in cancer Open access
Lara Sanoguera‐Miralles, Alberto Valenzuela‐Palomo, Elena Bueno Martínez, Ada Esteban‐Sánchez, Víctor Lorca, Inés Llinares‐Burguet, +8 more
14citations -
Molecular Genetic Screening in Patients With ACE Inhibitor/Angiotensin Receptor Blocker-Induced Angioedema to Explore the Role of Hereditary Angioedema Genes2022 Frontiers in Genetics article Medicine Coagulation, Bradykinin, Polyphosphates, and Angioedema Open access
Carina M. Mathey, Carlo Maj, Annika B. Scheer, Julia Fazaal, Bettina Wedi, Dorothea Wieczorek, +25 more
13citations -
Random forest and live single‐cell metabolomics reveal metabolic profiles of human macrophages upon polarization2023 Biotechnology and Bioengineering article Biochemistry, Genetics and Molecular Biology Metabolomics and Mass Spectrometry Studies Open access
Huaqi Tang, Ahmed Ali, Eman Muhammad Abdelazem, Tom H. M. Ottenhoff, Ron M. A. Heeren, Alireza Mashaghi
13citations -
The shifting lipidomic landscape of blood monocytes and neutrophils during pneumonia2024 JCI Insight article Biochemistry, Genetics and Molecular Biology Sphingolipid Metabolism and Signaling Open access
Alex R. Schuurman, Osoul Chouchane, Joe M. Butler, Hessel Peters Sengers, Sebastiaan C M Joosten, Xanthe Brands, +16 more
11citations -
A research intelligence approach to assess the research impact of the Dutch university medical centres2022 Health Research Policy and Systems article Decision Sciences scientometrics and bibliometrics research Open access
Rik Iping, Marielle E. Kroon, Chantal Steegers, Thed N. van Leeuwen
9citations -
A Novel Tool for the Analysis and Detection of Copy Number Variants Associated with Haemoglobinopathies2022 International Journal of Molecular Sciences article Medicine Hemoglobinopathies and Related Disorders Open access
Anna Minaidou, Stella Tamana, Coralea Stephanou, Maria Xenophontos, Cornelis L. Harteveld, Celeste Bento, +2 more
7citations -
Microduplications of ARID1A and ARID1B cause a novel clinical and epigenetic distinct BAFopathy2024 Genetics in Medicine article Biochemistry, Genetics and Molecular Biology Genomic variations and chromosomal abnormalities Open access
Pleuntje J. van der Sluijs, Sébastien Moutton, Alexander J.M. Dingemans, Denisa Weis, Michael A. Levy, Kym M. Boycott, +39 more
6citations -
The genome of New Zealand trevally (Carangidae: Pseudocaranx georgianus) uncovers a XY sex determination locus2021 bioRxiv (Cold Spring Harbor Laboratory) preprint Biochemistry, Genetics and Molecular Biology Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities Open access
Mike Ruigrok, Andrew S. Catanach, Deepa R. Bowatte, Marcus W. Davy, Roy D. Storey, Noémie Valenza-Troubat, +5 more
6citations -
UTILE-Pore: Deep Learning-Enabled 3D Analysis of Porous Materials in Polymer Electrolyte Membrane-Based Energy Devices2025 Journal of The Electrochemical Society article Engineering Fuel Cells and Related Materials Open access
André Colliard-Granero, Salvatore Ranieri, Aimy Bazylak, Tobias Morawietz, K. Andreas Friedrich, Jasna Janković, +3 more
5citations -
Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes2022 Molecular Cytogenetics article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access
Naomi Baba, Anna Lengyel, Éva Pinti, Elzem Yapici, Isolde Schreyer, Thomas Liehr, +2 more
5citations