June 10, 2019 article Open access Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders Genetics in Medicine DOI: 10.1038/s41436-019-0554-6 Full text (OA) OpenAlex Authors 0 Author list not loaded yet. Cited by 6 stored of 747 Search Sort Most cited Newest Oldest Patent citations Title Any typearticle review book-chapter conference-paper preprint dissertation book dataset other Any fieldAgricultural and Biological Sciences Arts and Humanities Biochemistry, Genetics and Molecular Biology Business, Management and Accounting Chemical Engineering Chemistry Computer Science Decision Sciences Dentistry Earth and Planetary Sciences Economics, Econometrics and Finance Energy Engineering Environmental Science Health Professions Immunology and Microbiology Materials Science Mathematics Medicine Neuroscience Nursing Pharmacology, Toxicology and Pharmaceutics Physics and Astronomy Psychology Social Sciences Veterinary Open access Verbesserung der interdisziplinären Zusammenarbeit zwischen den Fachgebieten Kinder- und Jugendpsychiatrie, und -psychotherapie sowie Humangenetik – Anregungen aus kinder- und jugendpsychiatrischer Sicht 2025 Medizinische Genetik article Decision Sciences Interdisciplinary Research and Collaboration Open access 1 citations Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses 2024 npj Genomic Medicine article Biochemistry, Genetics and Molecular Biology Genomics and Rare Diseases Open access 10 citations Reanalysis of whole-exome sequencing (WES) data of children with neurodevelopmental disorders in a standard patient care context 2023 European Journal of Pediatrics article Biochemistry, Genetics and Molecular Biology Genomics and Rare Diseases Open access 29 citations Reanalysis of whole-exome sequencing (WES) data of children with neurodevelopmental disorders in a standard patient care context 2023 Research Square preprint Biochemistry, Genetics and Molecular Biology Genomics and Rare Diseases Open access 4 citations Epigenotype–genotype–phenotype correlations in SETD1A and SETD2 chromatin disorders 2023 Human Molecular Genetics article Biochemistry, Genetics and Molecular Biology Genetics and Neurodevelopmental Disorders Open access 18 citations Genome-wide variant calling in reanalysis of exome sequencing data uncovered a pathogenic TUBB3 variant 2021 European Journal of Medical Genetics article Biochemistry, Genetics and Molecular Biology Genomics and Rare Diseases Open access 3 citations 6 results References 0