Not finding it? Sign in to also search OpenAlex live.
-
Genetic Risk Scores Identify Genetic Aetiology of Inflammatory Bowel Disease Phenotypes2020 Journal of Crohn s and Colitis article Biochemistry, Genetics and Molecular Biology Inflammatory Bowel Disease Open access
Lieke M. Spekhorst, Kimberley W. J. van der Sloot, Bernadien H. Jansen, Gerard D. H. Dijkstra, C. Janneke van der Woude, Frank Hoentjen, +7 more
15citations -
Phenotype-Agnostic Molecular Subtyping of Neurodegenerative Disorders: The Cincinnati Cohort Biomarker Program (CCBP)2020 Frontiers in Aging Neuroscience article Medicine Dementia and Cognitive Impairment Research Open access
Andrea Sturchio, Luca Marsili, Joaquín A. Vizcarra, Alok Kumar Dwivedi, Marcelo Andrés Kauffman, Andrew P. Duker, +18 more
38citations -
Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important2020 Journal of Molecular Medicine article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access
Thomas Eggermann, Johanna Brück, Cordula Knopp, György Fekete, Christian Peter Kratz, Velibor B. Tasic, +4 more
20citations -
Neurodevelopmental and other phenotypes recurrently associated with heterozygous BAZ2B loss‐of‐function variants2023 American Journal of Medical Genetics Part A article Biochemistry, Genetics and Molecular Biology Genetics and Neurodevelopmental Disorders Open access
Soha Sewani, Mahshid Sababi Azamian, Bryce A. Mendelsohn, Frédéric Tran Mau‐Them, Manon Réda, Sophie Nambot, +17 more
16citations -
Novel Genetic and Biochemical Insights into the Spectrum of NEFL -Associated Phenotypes2024 Journal of Neuromuscular Diseases article Neuroscience Hereditary Neurological Disorders Open access
Adela Della Marina, Andreas Hentschel, Artur Czech, Ulrike Schara, Corinna Preuße, Andreas Laner, +7 more
10citations -
Response to neoadjuvant chemotherapy and survival in molecular subtypes of resectable gastric cancer: a post hoc analysis of the D1/D2 and CRITICS trials
Hedde D. Biesma, Tanya T.D. Soeratram, Karolina Sikorska, Irene A. Caspers, Hendrik F. van Essen, Jacqueline M. P. Egthuijsen, +19 more
19citations -
Molecular Basis of Beckwith–Wiedemann Syndrome Spectrum with Associated Tumors and Consequences for Clinical Practice2022 Cancers article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access
Thomas Eggermann, Eamonn Richard Maher, Christian Peter Kratz, Dirk Prawitt
25citations -
Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis2024 Clinical Epigenetics article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access
Deborah Mackay, Gabriella E. Gazdagh, David Monk, Frédéric Brioude, Éloïse Giabicani, Izabela M. Krzyzewska, +26 more
25citations -
Taxonomic Revision of Eastern Part of Western Palaearctic Cordulegaster Using Molecular Phylogeny and Morphology, with the Description of Two New Species (Odonata: Anisoptera: Cordulegastridae)2021 Diversity article Agricultural and Biological Sciences Invertebrate Taxonomy and Ecology Open access
Thomas Schneider, Andy R. Vierstraete, Ole Müller, Gert Jan van Pelt, Max Caspers, Dietmar Ikemeyer, +2 more
25citations -
Implications of ad-hoc molecular typing for infection control measures in a multi-cluster, multi-phenotypic Serratia marcescens outbreak in a neonatal intensive care unit
Myrthe M. A. Toorop, Irene V Hoogendijk, H.C.M. Dogterom-Ballering, Stefan A. Boers, Margriet E. M. Kraakman, Joffrey van Prehn, +3 more
10citations -
Earthworm Coelomocyte Internalization of MoS2 Nanosheets: Multiplexed Imaging, Molecular Profiling, and Computational Modeling2023 Environmental Science & Technology article Engineering Graphene and Nanomaterials Applications Open access
Kailun Sun, Jason Christopher White, Erkai He, Cornelis A.M. van Gestel, Peng Zhang, Willie J.G.M. Peijnenburg, +1 more
6citations -
Models of KPTN-related disorder implicate mTOR signalling in cognitive and overgrowth phenotypes2023 Brain article Biochemistry, Genetics and Molecular Biology Genetics and Neurodevelopmental Disorders Open access
Maria O. Levitin, Lettie E. Rawlins, Gabriela Sánchez-Andrade, Osama A. Arshad, Stephan C. Collins, Stephen J. Sawiak, +35 more
12citations -
Distinct lipidomic profiles in breast cancer cell lines relate to proliferation and EMT phenotypes2025 Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids article Biochemistry, Genetics and Molecular Biology Cancer, Lipids, and Metabolism Open access
Hanneke Leegwater, Zhengzheng Zhang, Xiaobing Zhang, Xuesong Wang, Thomas Hankemeier, Annelien J.M. Zweemer, +6 more
3citations -
Mouse and cellular models of KPTN -related disorder implicate mTOR signalling in cognitive and progressive overgrowth phenotypes2022 bioRxiv (Cold Spring Harbor Laboratory) preprint Biochemistry, Genetics and Molecular Biology Genetics and Neurodevelopmental Disorders Open access
Maria O. Levitin, Lettie E. Rawlins, Gabriela Sánchez-Andrade, Osama A. Arshad, Stephan C. Collins, Stephen J. Sawiak, +35 more
1citations -
Context-dependent molecular responses to heterogeneous metabolic disease traits2026 medRxiv preprint Biochemistry, Genetics and Molecular Biology Bioinformatics and Genomic Networks Open access
Theodora-Dafni Michalettou, Sapna Sharma, Natalie N. Atabaki, Juan J. Fernandez-Tajes, Mun‐Gwan Hong, Jonathan Adam, +34 more
0citations -
Molecular signatures discriminating different types of rejection in human liver transplants2025 Journal of Hepatology article Medicine Organ Transplantation Techniques and Outcomes Open access
Bastian Engel, Ahmed Alaswad, Alejandro Campos-Murguía, Martijn Zoodsma, Anne Klingbeil, Pablo Ruíz, +21 more
10citations -
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings2024 Nature Genetics article Biochemistry, Genetics and Molecular Biology Genomics and Rare Diseases Open access
Axel Schmidt, Magdalena Danyel, Kathrin Grundmann, Theresa Brunet, Hannah Klinkhammer, Tzung‐Chien Hsieh, +93 more
56citations -
Delineating the molecular and phenotypic spectrum of the SETD1B -related syndrome2021 bioRxiv (Cold Spring Harbor Laboratory) preprint Biochemistry, Genetics and Molecular Biology Genetics and Neurodevelopmental Disorders Open access
Marjolein J.A. Weerts, Kristina Lanko, Francisco J. Guzmán‐Vega, Adam Jackson, Reshmi Ramakrishnan, Kelly J. Cardona‐Londoño, +91 more
0citations