TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations

Filiaciones

O'Rawe JA:

Stanley Institute for Cognitive Genomics, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA

Graduate Program in Genetics, Stony Brook University, Stony Brook, NY 11794, USA

Wu Y:

Stanley Institute for Cognitive Genomics, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA

Graduate Program in Genetics, Stony Brook University, Stony Brook, NY 11794, USA

Rope AF:

Department of Medical Genetics, Northwest Kaiser Permanente, Portland, OR 97227, USA

Au PY:

Department of Medical Genetics and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB T3B 6A8, Canada

Parboosingh JS:

Department of Medical Genetics and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB T3B 6A8, Canada

Moon S:

Center for Human Disease Modeling, Duke University, Durham, NC 27708, USA

Kousi M:

Center for Human Disease Modeling, Duke University, Durham, NC 27708, USA

Kosma K:

Department of Medical Genetics, Medical School, University of Athens, Athens 11527, Greece

Research Institute for the Study of Genetic and Malignant Disorders in Childhood, Aghia Sophia, Children's Hospital, Athens 11527, Greece

Smith CS:

Department of Medical Genetics and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB T3B 6A8, Canada

Tzetis M:

Department of Medical Genetics, Medical School, University of Athens, Athens 11527, Greece

Research Institute for the Study of Genetic and Malignant Disorders in Childhood, Aghia Sophia, Children's Hospital, Athens 11527, Greece

Schuette JL:

Department of Pediatrics, Division of Genetics, University of Michigan, Ann Arbor, MI 48109, USA

Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA

Hufnagel RB:

Division of Human Genetics, Cincinnati Children's Hospital, Cincinnati, OH 45229, USA

Unit on Pediatric, Developmental, and Genetic Ophthalmology, Ophthalmic Genetics and Visual Function Branch, National Eye Institute, NIH, Bethesda, MD 20892, USA

Prada CE:

Division of Human Genetics, Cincinnati Children's Hospital, Cincinnati, OH 45229, USA

Centro de Medicina Genómica y Metabolismo, Fundación Cardiovascular de Colombia, Bucaramanga, Santander 681004, Colombia

Martinez F:

Unidad de Genetica, Hospital Universitario y Politecnico La Fe, Valencia 46026, Spain

Orellana C:

Unidad de Genetica, Hospital Universitario y Politecnico La Fe, Valencia 46026, Spain

Caro-Llopis A:

Unidad de Genetica, Hospital Universitario y Politecnico La Fe, Valencia 46026, Spain

Oltra S:

Unidad de Genetica, Hospital Universitario y Politecnico La Fe, Valencia 46026, Spain

Monfort S:

Unidad de Genetica, Hospital Universitario y Politecnico La Fe, Valencia 46026, Spain

Jiménez-Barrón LT:

Stanley Institute for Cognitive Genomics, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA

Centro de Ciencias Genomicas, Universidad Nacional Autonoma de México, Cuernavaca, Morelos 62210, Mexico

Swensen J:

Caris Life Sciences, Phoenix, AZ 85040, USA

Ellingwood S:

Division of Genetics, Pediatric Specialty Care, Maine Medical Partners, ME 04102, USA

Smith R:

Department of Pediatrics, Division of Genetics, Barbara Bush Children's Hospital, Maine Medical Center, Portland, ME 04102, USA

Ospina S:

Fundacion Cardioinfantil and Universidad del Rosario, Bogota 681004, Colombia

Mittelman D:

Gene by Gene Ltd., Houston, TX 77008, USA

Highnam G:

Gene by Gene Ltd., Houston, TX 77008, USA

Robison R:

Utah Foundation for Biomedical Research, Salt Lake City, UT 84107, USA

Tute Genomics, 150 South 100 West Street, Provo, UT 84601, USA

Yang E:

Department of Radiology, Boston Children's Hospital, Boston, MA 02115, USA

Faivre L:

Génétique des Anomalies du Développement EA4271, Université Bourgogne Franche-Comté, 21000 Dijon, France

Centre de Génétique, Centre de Référence Maladies Rares "Anomalies du Développement et Syndromes Malformatifs," Centre Hospitalier Universitaire de Dijon, 21000 Dijon, France

Roubertie A:

Institut des Neurosciences de Montpellier, Université de Montpellier, BP 74103, 34950 Montpellier Cedex 5, France

Service de Neuropédiatrie, Centre Hospitalier Universitaire Gui de Chauliac, 34000 Montpellier, France

Monaghan KG:

GeneDx, Gaithersburg, MD 20877, USA

Wang K:

Zilkha Neurogenetic Institute, Department of Psychiatry and Preventive Medicine, University of Southern California, Los Angeles, CA 90089, USA

Davis EE:

Center for Human Disease Modeling, Duke University, Durham, NC 27708, USA

Katsanis N:

Center for Human Disease Modeling, Duke University, Durham, NC 27708, USA

Kalscheuer VM:

Research Group Development and Disease, Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany

Wang EH:

Department of Pharmacology, University of Washington, Seattle, WA 98195, USA

Metcalfe K:

Clinical Genetics Service, Manchester Centre for Genomic Medicine, Saint Mary's Hospital, Central Manchester University Hospitals NHS Foundation Trust, Oxford Road, Manchester M13 9WL, UK

Innes AM:

Department of Medical Genetics and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB T3B 6A8, Canada

Rosello M:

Unidad de Genetica, Hospital Universitario y Politecnico La Fe, Valencia 46026, Spain

Keegan CE:

Department of Pediatrics, Division of Genetics, University of Michigan, Ann Arbor, MI 48109, USA

Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA

Lyon GJ:

Stanley Institute for Cognitive Genomics, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA

Utah Foundation for Biomedical Research, Salt Lake City, UT 84107, USA.