Literature DB >> 24526565

Genomics into Healthcare: the 5th Pan Arab Human Genetics Conference and 2013 Golden Helix Symposium.

Paolo Fortina1, Najib Al Khaja, Mahmoud Taleb Al Ali, Abdul Rezzak Hamzeh, Pratibha Nair, Federico Innocenti, George P Patrinos, Larry J Kricka.   

Abstract

The joint 5th Pan Arab Human Genetics conference and 2013 Golden Helix Symposium, "Genomics into Healthcare" was coorganized by the Center for Arab Genomic Studies (http://www.cags.org.ae) in collaboration with the Golden Helix Foundation (http://www.goldenhelix.org) in Dubai, United Arab Emirates from 17 to 19 November, 2013. The meeting was attended by over 900 participants, doctors and biomedical students from over 50 countries and was organized into a series of nine themed sessions that covered cancer genomics and epigenetics, genomic and epigenetic studies, genomics of blood and metabolic disorders, cytogenetic diagnosis and molecular profiling, next-generation sequencing, consanguinity and hereditary diseases, clinical genomics, clinical applications of pharmacogenomics, and genomics in public health.
© 2014 WILEY PERIODICALS, INC.

Entities:  

Keywords:  NGS; cancer; diagnostics; epigenetics; genomics; meeting report

Mesh:

Year:  2014        PMID: 24526565      PMCID: PMC4128335          DOI: 10.1002/humu.22530

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  12 in total

Review 1.  Breast cancer in Arab populations: molecular characteristics and disease management implications.

Authors:  Lotfi Chouchane; Hammouda Boussen; Konduru S R Sastry
Journal:  Lancet Oncol       Date:  2013-09       Impact factor: 41.316

2.  Newborn screening: experiences in the Middle East and North Africa.

Authors:  A A Saadallah; M S Rashed
Journal:  J Inherit Metab Dis       Date:  2007-08-15       Impact factor: 4.982

Review 3.  Pharmacogenomics and public health: implementing 'populationalized' medicine.

Authors:  Lindsey Mette; Konstantinos Mitropoulos; Athanassios Vozikis; George P Patrinos
Journal:  Pharmacogenomics       Date:  2012-05       Impact factor: 2.533

4.  Screening for and prevention of type 2 diabetes.

Authors:  Elizabeth C Goyder
Journal:  BMJ       Date:  2008-04-21

Review 5.  CYP3A4*22: promising newly identified CYP3A4 variant allele for personalizing pharmacotherapy.

Authors:  Laure Elens; Teun van Gelder; Dennis A Hesselink; Vincent Haufroid; Ron H N van Schaik
Journal:  Pharmacogenomics       Date:  2013-01       Impact factor: 2.533

6.  Public Health Genomics and personalized healthcare: a pipeline from cell to society.

Authors:  Angela Brand
Journal:  Drug Metabol Drug Interact       Date:  2012

7.  A personal view on systems medicine and the emergence of proactive P4 medicine: predictive, preventive, personalized and participatory.

Authors:  Leroy Hood; Mauricio Flores
Journal:  N Biotechnol       Date:  2012-03-18       Impact factor: 5.079

8.  A novel mutation in PRG4 gene underlying camptodactyly-arthropathy-coxa vara-pericarditis syndrome with the possible expansion of the phenotype to include congenital cataract.

Authors:  Nadia A Akawi; Bassam R Ali; Lihadh Al-Gazali
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2012-06-08

9.  The Moroccan Genetic Disease Database (MGDD): a database for DNA variations related to inherited disorders and disease susceptibility.

Authors:  Hicham Charoute; Halima Nahili; Omar Abidi; Khalid Gabi; Hassan Rouba; Malika Fakiri; Abdelhamid Barakat
Journal:  Eur J Hum Genet       Date:  2013-07-17       Impact factor: 4.246

10.  Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays.

Authors:  Radoje Drmanac; Andrew B Sparks; Matthew J Callow; Aaron L Halpern; Norman L Burns; Bahram G Kermani; Paolo Carnevali; Igor Nazarenko; Geoffrey B Nilsen; George Yeung; Fredrik Dahl; Andres Fernandez; Bryan Staker; Krishna P Pant; Jonathan Baccash; Adam P Borcherding; Anushka Brownley; Ryan Cedeno; Linsu Chen; Dan Chernikoff; Alex Cheung; Razvan Chirita; Benjamin Curson; Jessica C Ebert; Coleen R Hacker; Robert Hartlage; Brian Hauser; Steve Huang; Yuan Jiang; Vitali Karpinchyk; Mark Koenig; Calvin Kong; Tom Landers; Catherine Le; Jia Liu; Celeste E McBride; Matt Morenzoni; Robert E Morey; Karl Mutch; Helena Perazich; Kimberly Perry; Brock A Peters; Joe Peterson; Charit L Pethiyagoda; Kaliprasad Pothuraju; Claudia Richter; Abraham M Rosenbaum; Shaunak Roy; Jay Shafto; Uladzislau Sharanhovich; Karen W Shannon; Conrad G Sheppy; Michel Sun; Joseph V Thakuria; Anne Tran; Dylan Vu; Alexander Wait Zaranek; Xiaodi Wu; Snezana Drmanac; Arnold R Oliphant; William C Banyai; Bruce Martin; Dennis G Ballinger; George M Church; Clifford A Reid
Journal:  Science       Date:  2009-11-05       Impact factor: 47.728

View more
  3 in total

1.  The genetics of rod-cone dystrophy in Arab countries: a systematic review.

Authors:  Hawraa Joumaa; Zamzam Mrad; Lama Jaffal; Christina Zeitz; Isabelle Audo; Said El Shamieh
Journal:  Eur J Hum Genet       Date:  2020-11-13       Impact factor: 5.351

Review 2.  Individualized medicine enabled by genomics in Saudi Arabia.

Authors:  Muhammad Abu-Elmagd; Mourad Assidi; Hans-Juergen Schulten; Ashraf Dallol; Peter Pushparaj; Farid Ahmed; Stephen W Scherer; Mohammed Al-Qahtani
Journal:  BMC Med Genomics       Date:  2015-01-15       Impact factor: 3.063

3.  Success stories in genomic medicine from resource-limited countries.

Authors:  Konstantinos Mitropoulos; Hayat Al Jaibeji; Diego A Forero; Paul Laissue; Ambroise Wonkam; Catalina Lopez-Correa; Zahurin Mohamed; Wasun Chantratita; Ming Ta Michael Lee; Adrian Llerena; Angela Brand; Bassam R Ali; George P Patrinos
Journal:  Hum Genomics       Date:  2015-06-18       Impact factor: 4.639

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.