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Catherine Nester, RN, Shares the Impact of Whole Genome Screening on Rare Disease

In this interview, Catherine Nester, RN explains the importance of entering phase 2 of the whole genome sequencing newborn screening program.

Catherine nesterInozyme pharmaPatient strategies

Catherine Nester, RN, Discusses the Advancement of the BeginNGS Screening Program

The BeginNGS program added 23 new founding members to the consortium and expanded to include 31 additional genetic disorders in its second phase screening, totaling 419 treatable genetic disorders.

Inozyme pharmaCatherine nesterScreening panelBeginngs consortiumRady children institute for genomic medicinePatient strategiesRady childrenGenomic medicineRecommended uniform screening panel

Form DEF 14A AMARIN CORP PLC\UK

Form DEF 14A AMARIN CORP PLC\UK
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New yorkUnited statesMemorial sloan kettering cancer centerNew jerseyPuerto ricoSeton hall universityCity ofUnited kingdomWest sussexNew zealandFordham universityRockefeller universityHong kongSaudi arabiaUniversity collegeNew south wales

New Study Shows Comprehensive Genomic Evidence is Critical for Calculating Rare Disease Prevalence

Ann Arbor, Michigan (PRWEB) December 15, 2022 Genomenon, Inc., an AI-driven genomics company, today announced the publication of a paper in the Orphanet

Inozyme pharmaMark kielCatherine nesterNational institutes of healthUniversity children hospitalGenomenon incVice presidentPatient strategiesOrphanet journalRare diseasesNational institutesUniversity childrenGenomenon chief scientific officerGenetic prevalence usingComprehensive literature reviewPress release

Co-Creating With Patients The New Guide To Expanded Access

Recently, Janssen Pharmaceutical Companies had the privilege of working with patients and advocacy groups to co-create a resource about expanded.

United statesBionical emasChristine maccrackenJanssen pharmaceutical companies of johnsonPatient strategies solutionsJanssen pharmaceuticalsPatient strategiesJanssen pharmaceutical companiesChief medical officerExpanded access

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