Literature DB >> 33350578

An online compendium of treatable genetic disorders.

David Bick1, Sarah L Bick2, David P Dimmock3, Tom A Fowler4,5, Mark J Caulfield4,5, Richard H Scott4,6.   

Abstract

More than 4,000 genes have been associated with recognizable Mendelian/monogenic diseases. When faced with a new diagnosis of a rare genetic disorder, health care providers increasingly turn to internet resources for information to understand the disease and direct care. Unfortunately, it can be challenging to find information concerning treatment for rare diseases as key details are scattered across a number of authoritative websites and numerous journal articles. The website and associated mobile device application described in this article begin to address this challenge by providing a convenient, readily available starting point to find treatment information. The site, Rx-genes.com (https://www.rx-genes.com/), is focused on those conditions where the treatment is directed against the mechanism of the disease and thereby alters the natural history of the disease. The website currently contains 633 disease entries that include references to disease information and treatment guidance, a brief summary of treatments, the inheritance pattern, a disease frequency (if known), nonmolecular confirmatory testing (if available), and a link to experimental treatments. Existing entries are continuously updated, and new entries are added as novel treatments appear in the literature.
© 2021 The Authors. American Journal of Medical Genetics Part C: Seminars in Medical Genetics published by Wiley Periodicals LLC.

Entities:  

Keywords:  genetic diseases; internet; mobile application; treatment

Mesh:

Year:  2020        PMID: 33350578      PMCID: PMC7986124          DOI: 10.1002/ajmg.c.31874

Source DB:  PubMed          Journal:  Am J Med Genet C Semin Med Genet        ISSN: 1552-4868            Impact factor:   3.908


  25 in total

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Authors:  Emma Reble; Mariana Gutierrez Salazar; Kathleen-Rose Zakoor; Sam Khalouei; Marc Clausen; Rita Kodida; Salma Shickh; Chloe Mighton; Iris Cohn; Kasmintan A Schrader; Raymond H Kim; Jordan Lerner-Ellis; Yvonne Bombard
Journal:  Hum Genet       Date:  2020-09-06       Impact factor: 4.132

2.  Assessment of a Highly Curated Somatic Oncology Database to Aid in the Interpretation of Clinically Important Variants in Next-Generation Sequencing Results.

Authors:  Stephanie J Yaung; Shuba Krishna; Liu Xi; Christine Ju; John F Palma; Maximilian Schmid
Journal:  J Mol Diagn       Date:  2020-09-19       Impact factor: 5.568

3.  Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project.

Authors:  Ozge Ceyhan-Birsoy; Jaclyn B Murry; Kalotina Machini; Matthew S Lebo; Timothy W Yu; Shawn Fayer; Casie A Genetti; Talia S Schwartz; Pankaj B Agrawal; Richard B Parad; Ingrid A Holm; Amy L McGuire; Robert C Green; Heidi L Rehm; Alan H Beggs
Journal:  Am J Hum Genet       Date:  2019-01-03       Impact factor: 11.025

4.  Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project.

Authors:  Tamara S Roman; Stephanie B Crowley; Myra I Roche; Ann Katherine M Foreman; Julianne M O'Daniel; Bryce A Seifert; Kristy Lee; Alicia Brandt; Chelsea Gustafson; Daniela M DeCristo; Natasha T Strande; Lori Ramkissoon; Laura V Milko; Phillips Owen; Sayanty Roy; Mai Xiong; Ryan S Paquin; Rita M Butterfield; Megan A Lewis; Katherine J Souris; Donald B Bailey; Christine Rini; Jessica K Booker; Bradford C Powell; Karen E Weck; Cynthia M Powell; Jonathan S Berg
Journal:  Am J Hum Genet       Date:  2020-08-26       Impact factor: 11.025

5.  Should states adopt newborn screening for early infantile Krabbe disease?

Authors:  David P Dimmock
Journal:  Genet Med       Date:  2016-02-04       Impact factor: 8.822

6.  International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases.

Authors:  Kym M Boycott; Ana Rath; Jessica X Chong; Taila Hartley; Fowzan S Alkuraya; Gareth Baynam; Anthony J Brookes; Michael Brudno; Angel Carracedo; Johan T den Dunnen; Stephanie O M Dyke; Xavier Estivill; Jack Goldblatt; Catherine Gonthier; Stephen C Groft; Ivo Gut; Ada Hamosh; Philip Hieter; Sophie Höhn; Matthew E Hurles; Petra Kaufmann; Bartha M Knoppers; Jeffrey P Krischer; Milan Macek; Gert Matthijs; Annie Olry; Samantha Parker; Justin Paschall; Anthony A Philippakis; Heidi L Rehm; Peter N Robinson; Pak-Chung Sham; Rumen Stefanov; Domenica Taruscio; Divya Unni; Megan R Vanstone; Feng Zhang; Han Brunner; Michael J Bamshad; Hanns Lochmüller
Journal:  Am J Hum Genet       Date:  2017-05-04       Impact factor: 11.025

7.  How genomic information is accessed in clinical practice: an electronic survey of UK general practitioners.

Authors:  W R H Evans; J Tranter; I Rafi; J Hayward; N Qureshi
Journal:  J Community Genet       Date:  2020-03-03

8.  Impact of Clinicians' Use of Electronic Knowledge Resources on Clinical and Learning Outcomes: Systematic Review and Meta-Analysis.

Authors:  Lauren A Maggio; Christopher A Aakre; Guilherme Del Fiol; Jane Shellum; David A Cook
Journal:  J Med Internet Res       Date:  2019-07-25       Impact factor: 5.428

9.  Next-generation sequencing of newborn screening genes: the accuracy of short-read mapping.

Authors:  C Trier; G Fournous; J M Strand; A Stray-Pedersen; R D Pettersen; A D Rowe
Journal:  NPJ Genom Med       Date:  2020-09-04       Impact factor: 8.617

10.  The role of exome sequencing in newborn screening for inborn errors of metabolism.

Authors:  Jennifer M Puck; Steven E Brenner; Aashish N Adhikari; Renata C Gallagher; Yaqiong Wang; Robert J Currier; George Amatuni; Laia Bassaganyas; Flavia Chen; Kunal Kundu; Mark Kvale; Sean D Mooney; Robert L Nussbaum; Savanna S Randi; Jeremy Sanford; Joseph T Shieh; Rajgopal Srinivasan; Uma Sunderam; Hao Tang; Dedeepya Vaka; Yangyun Zou; Barbara A Koenig; Pui-Yan Kwok; Neil Risch
Journal:  Nat Med       Date:  2020-08-10       Impact factor: 53.440

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  6 in total

1.  Developing a National Newborn Genomes Program: An Approach Driven by Ethics, Engagement and Co-design.

Authors:  Amanda Pichini; Arzoo Ahmed; Christine Patch; David Bick; Mathilde Leblond; Dalia Kasperaviciute; Dasha Deen; Simon Wilde; Sofia Garcia Noriega; Christella Matoko; Alice Tuff-Lacey; Chris Wigley; Richard H Scott
Journal:  Front Genet       Date:  2022-05-30       Impact factor: 4.772

2.  An online compendium of treatable genetic disorders.

Authors:  David Bick; Sarah L Bick; David P Dimmock; Tom A Fowler; Mark J Caulfield; Richard H Scott
Journal:  Am J Med Genet C Semin Med Genet       Date:  2020-12-22       Impact factor: 3.908

3.  Neural Networks for Classification and Image Generation of Aging in Genetic Syndromes.

Authors:  Dat Duong; Ping Hu; Cedrik Tekendo-Ngongang; Suzanna E Ledgister Hanchard; Simon Liu; Benjamin D Solomon; Rebekah L Waikel
Journal:  Front Genet       Date:  2022-04-11       Impact factor: 4.772

4.  An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseases.

Authors:  Mallory J Owen; Sebastien Lefebvre; Christian Hansen; Chris M Kunard; David P Dimmock; Laurie D Smith; Gunter Scharer; Rebecca Mardach; Mary J Willis; Annette Feigenbaum; Anna-Kaisa Niemi; Yan Ding; Luca Van Der Kraan; Katarzyna Ellsworth; Lucia Guidugli; Bryan R Lajoie; Timothy K McPhail; Shyamal S Mehtalia; Kevin K Chau; Yong H Kwon; Zhanyang Zhu; Sergey Batalov; Shimul Chowdhury; Seema Rego; James Perry; Mark Speziale; Mark Nespeca; Meredith S Wright; Martin G Reese; Francisco M De La Vega; Joe Azure; Erwin Frise; Charlene Son Rigby; Sandy White; Charlotte A Hobbs; Sheldon Gilmer; Gail Knight; Albert Oriol; Jerica Lenberg; Shareef A Nahas; Kate Perofsky; Kyu Kim; Jeanne Carroll; Nicole G Coufal; Erica Sanford; Kristen Wigby; Jacqueline Weir; Vicki S Thomson; Louise Fraser; Seka S Lazare; Yoon H Shin; Haiying Grunenwald; Richard Lee; David Jones; Duke Tran; Andrew Gross; Patrick Daigle; Anne Case; Marisa Lue; James A Richardson; John Reynders; Thomas Defay; Kevin P Hall; Narayanan Veeraraghavan; Stephen F Kingsmore
Journal:  Nat Commun       Date:  2022-07-26       Impact factor: 17.694

5.  Newborn Screening by Genomic Sequencing: Opportunities and Challenges.

Authors:  David Bick; Arzoo Ahmed; Dasha Deen; Alessandra Ferlini; Nicolas Garnier; Dalia Kasperaviciute; Mathilde Leblond; Amanda Pichini; Augusto Rendon; Aditi Satija; Alice Tuff-Lacey; Richard H Scott
Journal:  Int J Neonatal Screen       Date:  2022-07-15

Review 6.  A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases.

Authors:  Stephen F Kingsmore; Laurie D Smith; Chris M Kunard; Matthew Bainbridge; Sergey Batalov; Wendy Benson; Eric Blincow; Sara Caylor; Christina Chambers; Guillermo Del Angel; David P Dimmock; Yan Ding; Katarzyna Ellsworth; Annette Feigenbaum; Erwin Frise; Robert C Green; Lucia Guidugli; Kevin P Hall; Christian Hansen; Charlotte A Hobbs; Scott D Kahn; Mark Kiel; Lucita Van Der Kraan; Chad Krilow; Yong H Kwon; Lakshminarasimha Madhavrao; Jennie Le; Sebastien Lefebvre; Rebecca Mardach; William R Mowrey; Danny Oh; Mallory J Owen; George Powley; Gunter Scharer; Seth Shelnutt; Mari Tokita; Shyamal S Mehtalia; Albert Oriol; Stavros Papadopoulos; James Perry; Edwin Rosales; Erica Sanford; Steve Schwartz; Duke Tran; Martin G Reese; Meredith Wright; Narayanan Veeraraghavan; Kristen Wigby; Mary J Willis; Aaron R Wolen; Thomas Defay
Journal:  Am J Hum Genet       Date:  2022-08-24       Impact factor: 11.043

  6 in total

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