Variants in

PHF8 X-linked intellectual disability epigenetic gene regulation histone demethylation orofacial clefting

Journal

HGG advances
ISSN: 2666-2477
Titre abrégé: HGG Adv
Pays: United States
ID NLM: 101772885

Informations de publication

Date de publication:
14 Jul 2022
Historique:
received: 14 12 2021
accepted: 18 03 2022
entrez: 26 4 2022
pubmed: 27 4 2022
medline: 27 4 2022
Statut: epublish

Résumé

Loss-of-function variants in

Identifiants

pubmed: 35469323
doi: 10.1016/j.xhgg.2022.100102
pii: S2666-2477(22)00018-5
pmc: PMC9034099
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100102

Subventions

Organisme : NIGMS NIH HHS
ID : T32 GM008638
Pays : United States
Organisme : NICHD NIH HHS
ID : P50 HD105354
Pays : United States
Organisme : NHGRI NIH HHS
ID : U01 HG011744
Pays : United States
Organisme : NHGRI NIH HHS
ID : UM1 HG006493
Pays : United States
Organisme : NHGRI NIH HHS
ID : U24 HG008956
Pays : United States
Organisme : NIH HHS
ID : S10 OD021553
Pays : United States
Organisme : Wellcome Trust
Pays : United Kingdom

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2022 The Author(s).

Déclaration de conflit d'intérêts

J.J., J.Z., A.T., R.P., and K.M. are employees of GeneDx, Inc. All other authors have no conflict of interest to declare.

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Auteurs

Andrew K Sobering (AK)

AU/UGA Medical Partnership, Department of Basic Sciences, University of Georgia Health Sciences Campus, Athens, GA 30602, USA.
St. George's University, Department of Biochemistry, St. George's, Grenada, West Indies.
Windward Islands Research and Education Foundation, True Blue, St. George's, Grenada, West Indies.

Laura M Bryant (LM)

Center for Applied Genomics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Dong Li (D)

Center for Applied Genomics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Julie McGaughran (J)

Genetic Health Queensland, RBWH, Brisbane and The University of Queensland School of Medicine, Brisbane, QLD 4029, Australia.

Isabelle Maystadt (I)

Centre de Génétique Humaine, Institut de Pathologie et de Génétique, 6041 Gosselies, Belgium.

Stephanie Moortgat (S)

Centre de Génétique Humaine, Institut de Pathologie et de Génétique, 6041 Gosselies, Belgium.

John M Graham (JM)

Medical Genetics, Department of Pediatrics, Cedars-Sinai Medical Center, UCLA School of Medicine, Los Angeles, CA 90048, USA.

Arie van Haeringen (A)

Leiden University Medical Center, 9600, 2300 RC Leiden, the Netherlands.

Claudia Ruivenkamp (C)

Leiden University Medical Center, 9600, 2300 RC Leiden, the Netherlands.

Roos Cuperus (R)

Juliana Children's Hospital, HAGA Medical Center, The Hague, the Netherlands.

Julie Vogt (J)

Birmingham Women's and Children's NHS Foundation Trust, Birmingham Women's Hospital, Birmingham B15 2TG, UK.

Jenny Morton (J)

West Midlands Regional Clinical Genetics Service and Birmingham Health Partners, Birmingham Women's Hospital NHS Foundation Trust, Birmingham B15 2TG, UK.

Charlotte Brasch-Andersen (C)

Department of Clinical Genetics, Odense University Hospital, Odense 5000, Denmark.
Human Genetics, Department of Clinical Research, University of Southern Denmark, Odense 5000, Denmark.

Maria Steenhof (M)

Department of Clinical Genetics, Odense University Hospital, Odense 5000, Denmark.

Lars Kjærsgaard Hansen (LK)

Department of Paediatrics, Odense University Hospital, Odense 5000, Denmark.

Élodie Adler (É)

Fédération de Médecine Génomique and Imagine Institute, Université de Paris, Hôpital Necker-Enfants Malades, APHP, 75015 Paris, France.

Stanislas Lyonnet (S)

Fédération de Médecine Génomique and Imagine Institute, Université de Paris, Hôpital Necker-Enfants Malades, APHP, 75015 Paris, France.

Veronique Pingault (V)

Fédération de Médecine Génomique and Imagine Institute, Université de Paris, Hôpital Necker-Enfants Malades, APHP, 75015 Paris, France.

Marlin Sandrine (M)

Reference Center for Genetic Deafness, Fédération de Médecine Génomique and Imagine Institute, Université de Paris, Hôpital Necker-Enfants Malades, APHP, 75015 Paris, France.

Alban Ziegler (A)

Reference Center for Genetic Deafness, Fédération de Médecine Génomique and Imagine Institute, Université de Paris, Hôpital Necker-Enfants Malades, APHP, 75015 Paris, France.

Tyhiesia Donald (T)

Clinical Teaching Unit, St. George's University School of Medicine, St. George's, Grenada, West Indies.

Beverly Nelson (B)

Clinical Teaching Unit, St. George's University School of Medicine, St. George's, Grenada, West Indies.

Brandon Holt (B)

Department of Anatomical Sciences, St. George's University, Grenada, West Indies.

Oleksandra Petryna (O)

Hackensack University Ocean Medical Center, Department of Psychiatry, Hackensack, NJ 08724, USA.

Helen Firth (H)

Department of Clinical Genetics, Cambridge University Hospitals, Box 134, Cambridge CB2 0QQ, UK.

Kirsty McWalter (K)

Clinical Genomics, GeneDx, Gaithersburg, MD 20877, USA.

Jacob Zyskind (J)

Clinical Genomics, GeneDx, Gaithersburg, MD 20877, USA.

Aida Telegrafi (A)

Clinical Genomics, GeneDx, Gaithersburg, MD 20877, USA.

Jane Juusola (J)

Clinical Genomics, GeneDx, Gaithersburg, MD 20877, USA.

Richard Person (R)

Clinical Genomics, GeneDx, Gaithersburg, MD 20877, USA.

Michael J Bamshad (MJ)

Seattle Children's Hospital, Seattle, WA 98105, USA.
Departments of Pediatrics and Genome Sciences, University of Washington, Seattle, WA 98195, USA.
Brotman-Baty Institute, Seattle, WA 98195, USA.

Dawn Earl (D)

Seattle Children's Hospital, Seattle, WA 98105, USA.

Anne Chun-Hui Tsai (AC)

University of Oklahoma, Section of Genetics, 800 Stanton L Young Boulevard, Oklahoma City, OK 73117, USA.

Katherine R Yearwood (KR)

University Health Services, St. George's University, Grenada, West Indies.

Elysa Marco (E)

Cortica Healthcare, Marin Center, 4000 Civic Center Dr, Ste 100, San Rafael, CA 94903, USA.

Catherine Nowak (C)

Boston Children's Hospital, Division of Genetics and Genomics, 60 Temple Place, 2nd Floor, Boston, MA 02111, USA.

Jessica Douglas (J)

Boston Children's Hospital, Division of Genetics and Genomics, 60 Temple Place, 2nd Floor, Boston, MA 02111, USA.

Hakon Hakonarson (H)

Center for Applied Genomics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.

Elizabeth J Bhoj (EJ)

Center for Applied Genomics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.

Classifications MeSH