Summary of the first inaugural joint meeting of the International Consortium for scoliosis genetics and the International Consortium for vertebral anomalies and scoliosis, March 16-18, 2017, Dallas, Texas-Reference-Cited by-同舟云学术

Summary of the first inaugural joint meeting of the International Consortium for scoliosis genetics and the International Consortium for vertebral anomalies and scoliosis, March 16-18, 2017, Dallas, Texas

Published:2017-11-21 Issue:1 Volume:176 Page:253-256
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Giampietro Philip F.¹^ORCID,Pourquie Olivier²,Raggio Cathy³,Ikegawa Shiro⁴,Turnpenny Peter D.⁵,Gray Ryan⁶,Dunwoodie Sally L.⁷,Gurnett Christina A.⁸,Alman Benjamin⁹,Cheung Kenneth¹⁰,Kusumi Kenro¹¹,Hadley-Miller Nancy¹²,Wise Carol A.¹³¹⁴

Affiliation:

1. Drexel University College of Medicine; Philadelphia Pennsylvania

2. Harvard Medical School; Boston Massachusetts

3. Hospital for Special Surgery; New York New York

4. RIKEN Center for Integrative Medical Sciences; Tokyo Japan

5. Royal Devon and Exeter Hospital; Exeter United Kingdom

6. University of Texas; Austin Texas

7. Victor Chang Cardiac Research Institute; Darlinghurst New South Wales Australia

8. Washington University in St Louis; St. Louis Missouri

9. Duke University; Durham North Carolina

10. The University of Hong Kong; Hong Kong China

11. Arizona State University; Tempe Arizona

12. University of Colorado; Anschutz Medical Campus; Aurora Colorado

13. Texas Scottish Rite Hospital for Children; Dallas Texas

14. University of Texas Southwestern Medical Center; Dallas Texas

Funder

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Texas Scottish Rite Hospital for Children

Globus

Institut de France Fondation Yves Cotrel

Medtronic

Scoliosis Research Society

Nu Vasive

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference22 articles.

1. Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis;Buchan;Human Molecular Genetics,2014

2. Mutations in the MESP2 gene cause spondylothoracic dysostosis/Jarcho-Levin syndrome;Cornier;American Journal of Medical Genetics,2008

3. Phenotype characterization and natural history of spondylothoracic dysplasia syndrome: A series of 27 new cases;Cornier;American Journal of Medical Genetics Part A,2014

4. Scoliosis and segmentation defects of the vertebrae;Eckalbar;Wiley Interdiscip Reviews: Developmental Biology,2012

5. Genetic aspects of congenital and idiopathic scoliosis;Giampietro;Scientifica,2012

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2. Idiopathic scoliosis as a multifactorial disease: systematic review of current literature;Hirurgiâ pozvonočnika (Spine Surgery);2022-06-23

3. Congenital scoliosis: a narrative review and proposal of a treatment algorithm;EFORT Open Reviews;2022-05-01

4. Coding Variants Coupled With Rapid Modeling in Zebrafish Implicate Dynein Genes, dnaaf1 and zmynd10, as Adolescent Idiopathic Scoliosis Candidate Genes;Frontiers in Cell and Developmental Biology;2020-11-04

5. Identification of novel FBN1 variations implicated in congenital scoliosis;Journal of Human Genetics;2019-12-11