Correction: Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen)
Genetics in Medicine, Published online: 17 March 2021; doi:10.1038/s41436-021-01150-9Correction: Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen) (Source: Genetics in Medicine)
Source: Genetics in Medicine - March 17, 2021 Category: Genetics & Stem Cells Authors: Erin Rooney Riggs Erica F. Andersen Athena M. Cherry Sibel Kantarci Hutton Kearney Ankita Patel Gordana Raca Deborah I. Ritter Sarah T. South Erik C. Thorland Daniel Pineda-Alvarez Swaroop Aradhya Christa Lese Martin Source Type: research
DNA-based screening and population health: a points to consider statement for programs and sponsoring organizations from the American College of Medical Genetics and Genomics (ACMG)
Genetics in Medicine, Published online: 16 March 2021; doi:10.1038/s41436-020-01082-wDNA-based screening and population health: a points to consider statement for programs and sponsoring organizations from the American College of Medical Genetics and Genomics (ACMG) (Source: Genetics in Medicine)
Source: Genetics in Medicine - March 16, 2021 Category: Genetics & Stem Cells Authors: Michael F. Murray Monica A. Giovanni Debra L. Doyle Steven M. Harrison Elaine Lyon Kandamurugu Manickam Kristin G. Monaghan Sonja A. Rasmussen Maren T. Scheuner Glenn E. Palomaki Michael S. Watson Source Type: research
The underestimated burden of monogenic kidney disease in adults waitlisted for kidney transplantation
Genetics in Medicine, Published online: 12 March 2021; doi:10.1038/s41436-021-01127-8The underestimated burden of monogenic kidney disease in adults waitlisted for kidney transplantation (Source: Genetics in Medicine)
Source: Genetics in Medicine - March 12, 2021 Category: Genetics & Stem Cells Authors: Eva Schrezenmeier Elisa Kremerskothen Fabian Halleck Oliver Staeck Lutz Liefeldt Mira Choi Markus Sch üler Ulrike Weber Nadine Bachmann Maik Grohmann Timo Wagner Klemens Budde Carsten Bergmann Source Type: research
The intersection of genetics and COVID-19 in 2021: preview of the 2021 Rodney Howell Symposium
Genetics in Medicine, Published online: 12 March 2021; doi:10.1038/s41436-021-01113-0The intersection of genetics and COVID-19 in 2021: preview of the 2021 Rodney Howell Symposium (Source: Genetics in Medicine)
Source: Genetics in Medicine - March 12, 2021 Category: Genetics & Stem Cells Authors: Sonja A. Rasmussen Noura S. Abul-Husn Jean-Laurent Casanova Mark J. Daly Heidi L. Rehm Michael F. Murray Source Type: research
High diagnosis rate for nonimmune hydrops fetalis with prenatal clinical exome from the Hydrops-Yielding Diagnostic Results of Prenatal Sequencing (HYDROPS) Study
Genetics in Medicine, Published online: 08 March 2021; doi:10.1038/s41436-021-01121-0High diagnosis rate for nonimmune hydrops fetalis with prenatal clinical exome from the Hydrops-Yielding Diagnostic Results of Prenatal Sequencing (HYDROPS) Study (Source: Genetics in Medicine)
Source: Genetics in Medicine - March 8, 2021 Category: Genetics & Stem Cells Authors: Huda B. Al-Kouatly Mona M. Makhamreh Stephanie M. Rice Kelsey Smith Christopher Harman Andrea Quinn Breanna N. Valcarcel Brandy Firman Ruby Liu Madhuri Hegde Elizabeth Critchlow Seth I. Berger Source Type: research
Genome-wide investigation identifies a rare copy-number variant burden associated with human spina bifida
Genetics in Medicine, Published online: 08 March 2021; doi:10.1038/s41436-021-01126-9Genome-wide investigation identifies a rare copy-number variant burden associated with human spina bifida (Source: Genetics in Medicine)
Source: Genetics in Medicine - March 8, 2021 Category: Genetics & Stem Cells Authors: Paul Wolujewicz Vanessa Aguiar-Pulido Alice AbdelAleem Vidya Nair Gaurav Thareja Karsten Suhre Gary M. Shaw Richard H. Finnell Olivier Elemento M. Elizabeth Ross Source Type: research
Correction to: De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy
Genetics in Medicine, Published online: 08 March 2021; doi:10.1038/s41436-020-01090-wCorrection to: De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy (Source: Genetics in Medicine)
Source: Genetics in Medicine - March 8, 2021 Category: Genetics & Stem Cells Authors: Chiara Kl öckner Heinrich Sticht Pia Zacher Bernt Popp Holly E. Babcock Dewi P. Bakker Katy Barwick Michaela V. Bonfert Carsten G. B önnemann Eva H. Brilstra Wendy K. Chung Angus J. Clarke Patrick Devine Sandra Donkervoort Jamie L. Fraser Jennifer Fried Source Type: research
Clinical delineation, sex differences, and genotype–phenotype correlation in pathogenic KDM6A variants causing X-linked Kabuki syndrome type 2
Genetics in Medicine, Published online: 05 March 2021; doi:10.1038/s41436-021-01119-8Clinical delineation, sex differences, and genotype–phenotype correlation in pathogenic KDM6A variants causing X-linked Kabuki syndrome type 2 (Source: Genetics in Medicine)
Source: Genetics in Medicine - March 5, 2021 Category: Genetics & Stem Cells Authors: V íctor Faundes Stephanie Goh Rhoda Akilapa Heidre Bezuidenhout Hans T. Bjornsson Lisa Bradley Angela F. Brady Elise Brischoux-Boucher Han Brunner Saskia Bulk Natalie Canham Declan Cody Maria Lisa Dentici Maria Cristina Digilio Frances Elmslie Andrew E. Source Type: research
Addendum: American College of Medical Genetics consensus statement on factor V Leiden mutation testing
Genetics in Medicine, Published online: 05 March 2021; doi:10.1038/s41436-021-01108-xAddendum: American College of Medical Genetics consensus statement on factor V Leiden mutation testing (Source: Genetics in Medicine)
Source: Genetics in Medicine - March 5, 2021 Category: Genetics & Stem Cells Authors: Sucheta Bhatt Annette K. Taylor Reymundo Lozano Wayne W. Grody John H. Griffin Source Type: research
Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior
Genetics in Medicine, Published online: 03 March 2021; doi:10.1038/s41436-021-01114-zDisruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior (Source: Genetics in Medicine)
Source: Genetics in Medicine - March 3, 2021 Category: Genetics & Stem Cells Authors: Holly K. Harris Tojo Nakayama Jenny Lai Boxun Zhao Nikoleta Argyrou Cynthia S. Gubbels Aubrie Soucy Casie A. Genetti Victoria Suslovitch Lance H. Rodan George E. Tiller Gaetan Lesca Karen W. Gripp Reza Asadollahi Ada Hamosh Carolyn D. Applegate Peter D. T Source Type: research
The role of digital tools in the delivery of genomic medicine: enhancing patient-centered care
Genetics in Medicine, Published online: 02 March 2021; doi:10.1038/s41436-021-01112-1The role of digital tools in the delivery of genomic medicine: enhancing patient-centered care (Source: Genetics in Medicine)
Source: Genetics in Medicine - March 2, 2021 Category: Genetics & Stem Cells Authors: Salma Shickh Sara A. Rafferty Marc Clausen Rita Kodida Chloe Mighton Seema Panchal Justin Lorentz Thomas Ward Nicholas Watkins Christine Elser Andrea Eisen June C. Carroll Emily Glogowski Kasmintan A. Schrader Jordan Lerner-Ellis Raymond H. Kim David Chit Source Type: research
Taking an antiracist posture in scientific publications in human genetics and genomics
Genetics in Medicine, Published online: 01 March 2021; doi:10.1038/s41436-021-01109-wTaking an antiracist posture in scientific publications in human genetics and genomics (Source: Genetics in Medicine)
Source: Genetics in Medicine - March 1, 2021 Category: Genetics & Stem Cells Authors: Kyle B. Brothers Robin L. Bennett Mildred K. Cho Source Type: research
Correction: Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders
Genetics in Medicine, Published online: 26 February 2021; doi:10.1038/s41436-021-01130-zCorrection: Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders (Source: Genetics in Medicine)
Source: Genetics in Medicine - February 26, 2021 Category: Genetics & Stem Cells Authors: Bekim Sadikovic Michael A. Levy Jennifer Kerkhof Erfan Aref-Eshghi Laila Schenkel Alan Stuart Haley McConkey Peter Henneman Andrea Venema Charles E. Schwartz Roger E. Stevenson Steven A. Skinner Barbara R. DuPont Robin S. Fletcher Tugce B. Balci Victoria Source Type: research
The effect of early hormonal treatment (EHT) on expressive and receptive language capabilities in boys with 47,XXY (Klinefelter syndrome) during infancy and early childhood
Genetics in Medicine, Published online: 24 February 2021; doi:10.1038/s41436-021-01098-wThe effect of early hormonal treatment (EHT) on expressive and receptive language capabilities in boys with 47,XXY (Klinefelter syndrome) during infancy and early childhood (Source: Genetics in Medicine)
Source: Genetics in Medicine - February 24, 2021 Category: Genetics & Stem Cells Authors: Carole Samango-Sprouse Michaela Reiko Brooks Patricia Lasutchinkow Teresa Sadeghin Sherida Powell Mary Pat Hamzik Sophia Song Andrea L. Gropman Source Type: research
Expanding evidence leads to new pharmacogenomics payer coverage
Genetics in Medicine, Published online: 24 February 2021; doi:10.1038/s41436-021-01117-wExpanding evidence leads to new pharmacogenomics payer coverage (Source: Genetics in Medicine)
Source: Genetics in Medicine - February 24, 2021 Category: Genetics & Stem Cells Authors: Philip E. Empey Victoria M. Pratt James M. Hoffman Kelly E. Caudle Teri E. Klein Source Type: research
