Extending the allelic spectrum at noncoding risk loci of orofacial clefting-Reference-Cited by-同舟云学术

Extending the allelic spectrum at noncoding risk loci of orofacial clefting

Published:2021-06-03 Issue:8 Volume:42 Page:1066-1078
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Thieme Frederic¹^ORCID,Henschel Leonie¹,Hammond Nigel L.²,Ishorst Nina¹,Hausen Jonas³⁴,Adamson Antony D.²,Biedermann Angelika¹,Bowes John⁵,Zieger Hanna K.¹,Maj Carlo³,Kruse Teresa⁶,Buness Andreas³⁴,Hoischen Alexander⁷⁸⁹,Gilissen Christian⁷⁹,Kreusch Thomas¹⁰,Jäger Andreas¹¹,Gölz Lina¹¹¹²,Braumann Bert⁶,Aldhorae Khalid¹³,Rojas‐Martinez Augusto¹⁴,Krawitz Peter M.³,Mangold Elisabeth¹,Dixon Michael J.²,Ludwig Kerstin U.¹^ORCID

Affiliation:

1. Institute of Human Genetics, School of Medicine, University Hospital Bonn University of Bonn Bonn Germany

2. Faculty of Biology, Medicine, and Health, Manchester Academic Health Sciences Centre University of Manchester Manchester UK

3. School of Medicine, Institute of Genomic Statistics and Bioinformatics, University Hospital Bonn University of Bonn Bonn Germany

4. Department of Medical Biometry, Informatics, and Epidemiology, School of Medicine, University Hospital Bonn University of Bonn Bonn Germany

5. Arthritis Research UK Centre for Genetics and Genomics University of Manchester Manchester UK

6. Department of Orthodontics University of Cologne Cologne Germany

7. Department of Human Genetics Radboud University Medical Center Nijmegen The Netherlands

8. Department of Internal Medicine Radboud University Medical Center Nijmegen The Netherlands

9. Radboud Institute for Molecular Life Sciences Radboud University Medical Center Nijmegen The Netherlands

10. Department of Oral and Maxillofacial Surgery, Head and Neck Centre Asklepios Klinik Nord, Heidberg Hamburg Germany

11. Department of Orthodontics University of Bonn Bonn Germany

12. Department of Orthodontics University of Erlangen‐Nuremberg Erlangen Germany

13. Department of Orthodontics Thamar University Thamar Yemen

14. Tecnologico de Monterrey, Escuela de Medicina y Ciencias de la Salud, and Universidad Autonoma de Nuevo Leon Centro de Investigación y Desarrollo en Ciencias de la Salud Monterrey Mexico

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.24219

Reference62 articles.

1. Nonsyndromic cleft lip with or without cleft palate in arab populations: Genetic analysis of 15 risk loci in a novel case–control sample recruited in Yemen

2. Fine Tuning of Craniofacial Morphology by Distant-Acting Enhancers

3. Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromes

4. Annotation of functional variation in personal genomes using RegulomeDB

5. MIPgen: optimized modeling and design of molecular inversion probes for targeted resequencing

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1. Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores;Molecular Genetics & Genomic Medicine;2022-12-05

2. Molecular Genetic Screening in Patients With ACE Inhibitor/Angiotensin Receptor Blocker-Induced Angioedema to Explore the Role of Hereditary Angioedema Genes;Frontiers in Genetics;2022-07-18

3. Genetic models and approaches to study orofacial clefts;Oral Diseases;2022-01-06