Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders-Reference-Cited by-同舟云学术

Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders

Published:2018-09-02 Issue:9 Volume:13 Page:897-909
ISSN:1559-2294
Container-title:Epigenetics
language:en
Short-container-title:Epigenetics

Author:

Fontana L.¹^ORCID,Bedeschi M. F.²,Maitz S.³,Cereda A.⁴,Faré C.⁵,Motta S.⁵,Seresini A.⁶⁷,D’Ursi P.⁸,Orro A.⁸^ORCID,Pecile V.⁹,Calvello M.⁵¹⁰,Selicorni A.¹¹,Lalatta F.²,Milani D.¹²^ORCID,Sirchia S. M.¹³^ORCID,Miozzo M.¹⁵^ORCID,Tabano S.¹^ORCID

Affiliation:

1. Laboratory of Molecular Pathology, Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Milano, Italy

2. Clinical Genetics Unit, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milano, Italy

3. Clinical Pediatric, Genetics Unit, MBBM Foundation, San Gerardo Monza, Monza, Italy

4. Medical Genetics Unit, Papa Giovanni XXIII Hospital, Bergamo, Italy

5. Division of Pathology, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milano, Italy

6. Medical Genetics Laboratory, Fondazione IRCCS Ca’ Granda - Ospedale Maggiore Policlinico, Milano, Italy

7. Fondazione Grigioni per il Morbo di Parkinson, Milano, Italy

8. Department of Biomedical Sciences National Research Council, Institute for Biomedical Technologies, Segrate, Italy

9. Medical Genetics Division, Institute for maternal and child health IRCCS Burlo Garofolo, Trieste, Italy

10. Division of Cancer Prevention and Genetics, IEO, European Institute of Oncology IRCCS, Milano, Italy

11. UOC Pediatria, ASST Lariana, Como, Italy

12. Pediatric Highly Intensive Care Unit, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milano, Italy

13. Medical Genetics, Department of Health Sciences, Università degli Studi di Milano, Milano, Italy

Funder

Ministero della Salute and Regione Lombardia

Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico

Flagship ‘InterOmics’

Fondazione Regionale per la Ricerca Biomedica

Publisher

Informa UK Limited

Subject

Cancer Research,Molecular Biology

Link

https://www.tandfonline.com/doi/pdf/10.1080/15592294.2018.1514230

Reference43 articles.

1. Beckwith–Wiedemann syndrome

2. A prospective study validating a clinical scoring system and demonstrating phenotypical-genotypical correlations in Silver-Russell syndrome

3. Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome

4. 11p15 Imprinting Center Region 1 Loss of Methylation Is a Common and Specific Cause of Typical Russell-Silver Syndrome: Clinical Scoring System and Epigenetic-Phenotypic Correlations

5. Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjects

Cited by 25 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis;Clinical Epigenetics;2024-08-01

2. Approach to the Patient With Suspected Silver-Russell Syndrome;The Journal of Clinical Endocrinology & Metabolism;2024-06-18

3. Maternal loss-of-function of Nlrp2 results in failure of epigenetic reprogramming in mouse oocytes;2024-06-04

4. Genetics and Epigenetics of Precocious Puberty;Russian Journal of Genetics;2023-12

5. Genetics and Epigenetics of Precocious Puberty;Генетика;2023-12-01