September 23, 2019 article Open access IGF2 Mutations The Journal of Clinical Endocrinology & Metabolism DOI: 10.1210/clinem/dgz034 Full text (OA) OpenAlex Authors 0 Author list not loaded yet. Cited by 8 stored of 40 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 Copy Number Variants in the 11p15.5 Associated Imprinting Disorders: An Attempt to Establish a Genotype–Phenotype Correlation 2026 Clinical Genetics article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access 1 citations Human Reproduction and Disturbed Genomic Imprinting 2024 Genes article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access 9 citations Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes 2022 Molecular Cytogenetics article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access 5 citations Growth Restriction and Genomic Imprinting-Overlapping Phenotypes Support the Concept of an Imprinting Network 2021 Genes article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access 38 citations Unusual deletion of the maternal 11p15 allele in Beckwith–Wiedemann syndrome with an impact on both imprinting domains 2021 Clinical Epigenetics article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access 10 citations One test for all: whole exome sequencing significantly improves the diagnostic yield in growth retarded patients referred for molecular testing for Silver–Russell syndrome 2021 Orphanet Journal of Rare Diseases article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access 25 citations Novel mutation points to a hot spot in CDKN1C causing Silver–Russell syndrome 2020 Clinical Epigenetics article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access 21 citations HMGA2 Variants in Silver-Russell Syndrome: Homozygous and Heterozygous Occurrence 2020 The Journal of Clinical Endocrinology & Metabolism article Biochemistry, Genetics and Molecular Biology Genomics and Rare Diseases Open access 27 citations 8 results References 0