Front Cover, Volume 43, Issue 10
Sheng-Jia Lin
Genes & Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, USA
Search for more papers by this authorCorresponding Author
Barbara Vona
Institute of Human Genetics, Julius Maximilians University Würzburg, Würzburg, Germany
Institute for Auditory Neuroscience and InnerEarLab, University Medical Center Göttingen, Göttingen, Germany
Institute of Human Genetics, University Medical Center Göttingen, Göttingen, Germany
Correspondence Barbara Vona, Institute for Auditory Neuroscience & InnerEarLab, University Medical Center Göttingen, Göttingen, Germany.
Email: [email protected]
Gaurav K. Varshney, Genes & Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 73104, USA.
Email: [email protected]
Search for more papers by this authorHillary M. Porter
Children's National Hospital, Rare Disease Institute, Washington, District of Columbia, USA
Search for more papers by this authorMahmoud Izadi
Division of Genomics and Translational Medicine, College of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar
Search for more papers by this authorKevin Huang
Genes & Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, USA
Search for more papers by this authorYves Lacassie
Department of Pediatrics, Louisiana State University Health Sciences Center, Head Division of Clinical Genetics and Dept. of Genetics Children's Hospital 1986-2016, New Orleans, Los Angeles, USA
Search for more papers by this authorJill A. Rosenfeld
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA
Baylor Genetics Laboratories, Houston, Texas, USA
Search for more papers by this authorSaadullah Khan
Department of Biotechnology and Genetic Engineering, Kohat University of Science & Technology, Kohat, Khyber Pakhtunkhwa, Pakistan
Search for more papers by this authorCassidy Petree
Genes & Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, USA
Search for more papers by this authorTayyiba A. Ali
Division of Genomics and Translational Medicine, College of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar
Search for more papers by this authorNazif Muhammad
Department of Biotechnology and Genetic Engineering, Kohat University of Science & Technology, Kohat, Khyber Pakhtunkhwa, Pakistan
Search for more papers by this authorSher A. Khan
Department of Biotechnology and Genetic Engineering, Kohat University of Science & Technology, Kohat, Khyber Pakhtunkhwa, Pakistan
Search for more papers by this authorNoor Muhammad
Department of Biotechnology and Genetic Engineering, Kohat University of Science & Technology, Kohat, Khyber Pakhtunkhwa, Pakistan
Search for more papers by this authorPengfei Liu
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA
Baylor Genetics Laboratories, Houston, Texas, USA
Search for more papers by this authorMarie-Louise Haymon
Children Hospital New Orleans Louisiana, Pediatric Radiology, Tulane Associate Professor of Radiology, New Orleans, Los Angeles, USA
Search for more papers by this authorFranz Rüschendorf
Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany
Search for more papers by this authorIl-Keun Kong
Department of Animal Sciences, Division of Applied Life Science (BK21 Four), Gyeongsang National University, Jinju, South Korea
Search for more papers by this authorLinda Schnapp
Institute of Human Genetics, Julius Maximilians University Würzburg, Würzburg, Germany
Search for more papers by this authorNatasha Shur
Children's National Hospital, Rare Disease Institute, Washington, District of Columbia, USA
Search for more papers by this authorLynn Chorich
Section of Reproductive Endocrinology, Infertility & Genetics, Department of Obstetrics and Gynecology, Department of Neuroscience and Regenerative Medicine, Medical College of Georgia, Augusta University, Augusta, USA
Search for more papers by this authorLawrence Layman
Section of Reproductive Endocrinology, Infertility & Genetics, Department of Obstetrics and Gynecology, Department of Neuroscience and Regenerative Medicine, Medical College of Georgia, Augusta University, Augusta, USA
Search for more papers by this authorThomas Haaf
Institute of Human Genetics, Julius Maximilians University Würzburg, Würzburg, Germany
Search for more papers by this authorEhsan Pourkarimi
Division of Genomics and Translational Medicine, College of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar
Search for more papers by this authorHyung-Goo Kim
Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar
Search for more papers by this authorCorresponding Author
Gaurav K. Varshney
Genes & Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, USA
Correspondence Barbara Vona, Institute for Auditory Neuroscience & InnerEarLab, University Medical Center Göttingen, Göttingen, Germany.
Email: [email protected]
Gaurav K. Varshney, Genes & Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 73104, USA.
Email: [email protected]
Search for more papers by this authorSheng-Jia Lin
Genes & Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, USA
Search for more papers by this authorCorresponding Author
Barbara Vona
Institute of Human Genetics, Julius Maximilians University Würzburg, Würzburg, Germany
Institute for Auditory Neuroscience and InnerEarLab, University Medical Center Göttingen, Göttingen, Germany
Institute of Human Genetics, University Medical Center Göttingen, Göttingen, Germany
Correspondence Barbara Vona, Institute for Auditory Neuroscience & InnerEarLab, University Medical Center Göttingen, Göttingen, Germany.
Email: [email protected]
Gaurav K. Varshney, Genes & Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 73104, USA.
Email: [email protected]
Search for more papers by this authorHillary M. Porter
Children's National Hospital, Rare Disease Institute, Washington, District of Columbia, USA
Search for more papers by this authorMahmoud Izadi
Division of Genomics and Translational Medicine, College of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar
Search for more papers by this authorKevin Huang
Genes & Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, USA
Search for more papers by this authorYves Lacassie
Department of Pediatrics, Louisiana State University Health Sciences Center, Head Division of Clinical Genetics and Dept. of Genetics Children's Hospital 1986-2016, New Orleans, Los Angeles, USA
Search for more papers by this authorJill A. Rosenfeld
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA
Baylor Genetics Laboratories, Houston, Texas, USA
Search for more papers by this authorSaadullah Khan
Department of Biotechnology and Genetic Engineering, Kohat University of Science & Technology, Kohat, Khyber Pakhtunkhwa, Pakistan
Search for more papers by this authorCassidy Petree
Genes & Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, USA
Search for more papers by this authorTayyiba A. Ali
Division of Genomics and Translational Medicine, College of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar
Search for more papers by this authorNazif Muhammad
Department of Biotechnology and Genetic Engineering, Kohat University of Science & Technology, Kohat, Khyber Pakhtunkhwa, Pakistan
Search for more papers by this authorSher A. Khan
Department of Biotechnology and Genetic Engineering, Kohat University of Science & Technology, Kohat, Khyber Pakhtunkhwa, Pakistan
Search for more papers by this authorNoor Muhammad
Department of Biotechnology and Genetic Engineering, Kohat University of Science & Technology, Kohat, Khyber Pakhtunkhwa, Pakistan
Search for more papers by this authorPengfei Liu
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA
Baylor Genetics Laboratories, Houston, Texas, USA
Search for more papers by this authorMarie-Louise Haymon
Children Hospital New Orleans Louisiana, Pediatric Radiology, Tulane Associate Professor of Radiology, New Orleans, Los Angeles, USA
Search for more papers by this authorFranz Rüschendorf
Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany
Search for more papers by this authorIl-Keun Kong
Department of Animal Sciences, Division of Applied Life Science (BK21 Four), Gyeongsang National University, Jinju, South Korea
Search for more papers by this authorLinda Schnapp
Institute of Human Genetics, Julius Maximilians University Würzburg, Würzburg, Germany
Search for more papers by this authorNatasha Shur
Children's National Hospital, Rare Disease Institute, Washington, District of Columbia, USA
Search for more papers by this authorLynn Chorich
Section of Reproductive Endocrinology, Infertility & Genetics, Department of Obstetrics and Gynecology, Department of Neuroscience and Regenerative Medicine, Medical College of Georgia, Augusta University, Augusta, USA
Search for more papers by this authorLawrence Layman
Section of Reproductive Endocrinology, Infertility & Genetics, Department of Obstetrics and Gynecology, Department of Neuroscience and Regenerative Medicine, Medical College of Georgia, Augusta University, Augusta, USA
Search for more papers by this authorThomas Haaf
Institute of Human Genetics, Julius Maximilians University Würzburg, Würzburg, Germany
Search for more papers by this authorEhsan Pourkarimi
Division of Genomics and Translational Medicine, College of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar
Search for more papers by this authorHyung-Goo Kim
Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar
Search for more papers by this authorCorresponding Author
Gaurav K. Varshney
Genes & Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, USA
Correspondence Barbara Vona, Institute for Auditory Neuroscience & InnerEarLab, University Medical Center Göttingen, Göttingen, Germany.
Email: [email protected]
Gaurav K. Varshney, Genes & Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 73104, USA.
Email: [email protected]
Search for more papers by this authorSheng-Jia Lin and Barbara Vona should be considered joint first authors.
Graphical Abstract
Front Cover: The cover image is based on the Research Article Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function by Sheng-Jia Lin et al., https://doi.org/10.1002/humu.24435.
