July 26, 2012 article Open access Clinical significance of copy number variations in the 11p15.5 imprinting control regions: new cases and review of the literature Journal of Medical Genetics DOI: 10.1136/jmedgenet-2012-100967 Full text (OA) OpenAlex Authors 0 Author list not loaded yet. Cited by 7 stored of 111 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 Diagnosis and management of Silver–Russell syndrome: second international consensus statement 2026 Nature Reviews Endocrinology review Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access 0 citations 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 Further understanding of paternal uniparental disomy in Beckwith-Wiedemann syndrome 2022 Expert Review of Endocrinology & Metabolism article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting 7 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 Disorders of IGFs and IGF-1R signaling pathways 2020 Molecular and Cellular Endocrinology article Medicine Growth Hormone and Insulin-like Growth Factors Open access 151 citations Heterogeneous phenotypes in families with duplications of the paternal allele within the imprinting center 1 ( H19 / IGF2 : TSS‐DMR ) in 11p15.5 2020 Clinical Genetics article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting 7 citations Paternal 132 bp deletion affecting KCNQ1OT1 in 11p15.5 is associated with growth retardation but does not affect imprinting 2020 Journal of Medical Genetics article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting 14 citations 7 results References 0