Genetic and Genomic Medicine

A novel gene ZNF862 causes hereditary gingival fibromatosis

1. Juan Wu
2. Dongna Chen
3. Hui Huang
4. Ning Luo
5. Huishuang Chen
6. Junjie Zhao
7. Yanyan Wang
8. Tian Zhao
9. Siyuan Huang
10. Yang Ren
11. Teng Zhai
12. Weibin Sun
13. Houxuan Li
14. Wei Li

• Curated by eLife

  Evaluation Summary:

  This work is of clinical relevance to those interested in the etiology and pathology of hereditary gingival fibromatosis (HGF). The paper discusses two novel findings: identification of a causative role of a missense mutation in the gene encoding the zinc finger protein 862 (ZNF862) that leads to hereditary gingival fibromatosis (HGF), a rare disease characterized by overgrowth of gingivae, in an examined family, and a suggestion of the molecular consequences of that mutation that leads to the disease.

  (This preprint has been reviewed by eLife. We include the public reviews from the reviewers here; the authors also receive private feedback with suggested changes to the manuscript. Reviewer #1 and Reviewer #3 agreed to share their name with the authors.)

Reviewed by eLife

SARS-CoV-2 Genetic Diversity and Lineage Dynamics in Egypt during the First 18 Months of the Pandemic

1. Wael H. Roshdy
2. Mohamed K. Khalifa
3. James Emmanuel San
4. Houriiyah Tegally
5. Eduan Wilkinson
6. Shymaa Showky
7. Darren Patrick Martin
8. Monika Moir
9. Amel Naguib
10. Nancy Elguindy
11. Mokhtar R. Gomaa
12. Manal Fahim
13. Hanaa Abu Elsood
14. Amira Mohsen
15. Ramy Galal
16. Mohamed Hassany
17. Richard J. Lessells
18. Ahmed A. Al-Karmalawy
19. Rabeh EL-Shesheny
20. Ahmed M. Kandeil
21. Mohamed A. Ali
22. Tulio de Oliveira

Reviewed by ScreenIT

Amplicon-based nanopore minion sequencing of patients with COVID-19 omicron variant from India

1. Somesh Kumar
2. Avinash Lomash
3. Mohammed Faruq
4. Oves Siddiqui
5. Suresh Kumar
6. Seema Kapoor
7. Prashanth Suravajhala
8. Sunil K Polipalli
9. SCOG_MAMC_ LNH

Reviewed by ScreenIT

Tracking mutational semantics of SARS-CoV-2 genomes

1. Rohan Singh
2. Sunil Nagpal
3. Nishal K. Pinna
4. Sharmila S. Mande

Reviewed by ScreenIT

Minimal observed impact of HLA genotype on hospitalization and severity of SARS‐CoV ‐2 infection

1. Austin Nguyen
2. Tasneem Yusufali
3. Jill A. Hollenbach
4. Abhinav Nellore
5. Reid F. Thompson

Reviewed by ScreenIT

The Omicron variant mutation at position 28,311 in the SARS-CoV-2 N gene does not perturb CDC N1 target detection

1. Yanxia Bei
2. Kyle B. Vrtis
3. Janine G. Borgaro
4. Bradley W. Langhorst
5. Nicole M. Nichols

Reviewed by ScreenIT

Early detection and improved genomic surveillance of SARS-CoV-2 variants from deep sequencing data

1. Daniele Ramazzotti
2. Davide Maspero
3. Fabrizio Angaroni
4. Silvia Spinelli
5. Marco Antoniotti
6. Rocco Piazza
7. Alex Graudenzi

Reviewed by ScreenIT

Phenome‐Wide Association Study of Severe COVID‐19 Genetic Risk Variants

1. Jessica A. Regan
2. Jawan W. Abdulrahim
3. Nathan A. Bihlmeyer
4. Carol Haynes
5. Lydia Coulter Kwee
6. Manesh R. Patel
7. Svati H. Shah

Reviewed by ScreenIT

Genetic overlap between idiopathic pulmonary fibrosis and COVID-19

1. Richard J. Allen
2. Beatriz Guillen-Guio
3. Emma Croot
4. Luke M. Kraven
5. Samuel Moss
6. Iain Stewart
7. R. Gisli Jenkins
8. Louise V. Wain

Reviewed by ScreenIT

Inexpensive and colorimetric RNA detection by E. coli cell-free protein synthesis platform at room temperature

1. Michela Notarangelo
2. Alessandro Quattrone
3. Massimo Pizzato
4. Sheref S. Mansy
5. Ö. Duhan Toparlak

Reviewed by ScreenIT