Webinars | Blueprint Genetics

Keeping Pace: The Importance of a Shared Care Approach to Inherited Cardiovascular Disease

Date: 30 Oct, 2019

Time: 8:30 PST / 16:30 CET

Duration: 1 hour

Speaker: Dr. Andrew Krahn

Webinars

Introducing an open access genetic testing program for patients with inherited retinal degeneration

Date: 24 Oct, 2019

Time: 12:00pm-1pm EST

Duration: 1 hour

Speaker: T. Alastalo, K. Trzupek, B. Shaberman

Webinars

Genetic Testing for Individuals with Kidney Disease: Updates and Clinical Utility

Date: 03 Oct, 2019

Time: 11 am ET / 5 pm CEST

Duration: 1 hour

Speaker: Dr. Friedhelm Hildebrandt (MD)

Webinars

How to solve challenging cases? Part II

Date: 27 Aug, 2019

Time: 8:30 PST / 17:30 CEST

Duration: 60:00

Speaker: Johanna Sistonen (PhD)

Webinars

Behind the scenes: What it actually takes to make a genetic test

Date: 24 Jun, 2019

Time: 11:30 EDT / 17:30 CEST

Duration: 60:00

Speaker: Samuel Myllykangas, PhD

Webinars

Talk: Emerging opportunities in resolving difficult-to-sequence regions – PKD1 as a case example

Date: 15 Jun, 2019

Time: 1 pm - 1:45 pm

Duration: 34:22

Speaker: Johanna Sistonen, PhD

Webinars

Talk: High resolution CNV detection – a powerful diagnostic tool

Date: 15 Jun, 2019

Time: 12:15 pm -1 pm

Duration: 40:11

Speaker: Eveliina Salminen (MD, PhD)

Webinars

How to solve challenging cases? Part I

Date: 29 May, 2019

Time: 09:00 PDT / 18:00 CEST

Duration: 60:00

Speaker: Jennifer Schleit, Lucia Guidugli

Webinars

What if it’s a variant of uncertain significance (VUS)?

Date: 30 Apr, 2019

Time: 09am PDT / 18pm CEST

Duration: 60:00

Speaker: Jennifer Schleit, PhD FACMG

Webinars

Talk: Improved Diagnostic Yield in Rare Hereditary Disorders -Meeting Clinical Needs Using Customized Whole Exome Sequencing Solutions

Date: 04 Apr, 2019

Time: 12:30pm PT

Duration: 26:06

Speaker: Kim Gall, MSc, CGC, LGC

Webinars

High quality genetic diagnostics of polycystic kidney disease with NGS technology

Date: 26 Mar, 2019

Time: 09am PT / 17pm CET

Duration: 60:00

Speaker: Tero-Pekka Alastalo, MD, PhD

Webinars

Genetic Testing to enhance the value of a patient registry – A case study in the Inherited Retinal Dystrophies

Date: 26 Feb, 2019

Time: 1 pm EST / 19 pm CET

Duration: 1 hour

Speaker: K. Branham, K. Trzupek, T. Alastalo

Webinars

Getting the most from exomes

Date: 06 Feb, 2019

Time: 18pm CET / 09am PT

Duration: 60:00

Speaker: Jennifer Schleit, PhD FACMG

Webinars

Shedding light on complex regions in genetics

Date: 20 Nov, 2018

Time: 18:00 pm CET / 9:00 am PT

Duration: 43:23

C.E.U: -

Speaker: Johanna Sistonen, PhD

Webinars

Utility of genetic testing and application to immune-related disorders

Date: 25 Oct, 2018

Time: 18:00 pm CEST / 9:00 am PDT

Duration: 47:36

C.E.U: -

Speaker: Lucia Guidugli, PhD, FACMG

Webinars

Nucleus – Faster and easier access to ordering genetic testing for your patient

Date: 25 Sep, 2018

Time: 6:00 pm CEST / 9:00 am PST

Duration: 24:16

C.E.U: -

Speaker: Thomas Vincent

Webinars

Raising the bar: What to expect from cardiovascular genetic testing in 2018

Date: 28 Jun, 2018

Time: 7:00 pm - 8:00 pm EEST

Duration: 1:06

C.E.U: -

Speaker: Julie Hathaway, Dr. Tero-Pekka Alastalo

Webinars

Understanding Variants of Uncertain Significance

Date: 23 Apr, 2018

Time: 9:00 am - 10:00 am PST

Duration: 41:34

C.E.U: -

Speaker: Jennifer Schleit

Webinars

Genetic Diagnostics and Targeted Therapies of Primary Immunodeficiency Diseases (PID)

Date: 19 Apr, 2018

Time: 12:00 pm - 13:00 pm PST

Duration: 37:05

C.E.U: -

Speaker: Dr. Jolan E. Walter

Webinars

Utilization of NGS in Genetic Diagnostics of Inherited Retinal Diseases with Panel Update

Date: 14 Mar, 2018

Time: 12:00 pm - 13:00 pm PDT

Duration: 46:23

C.E.U: -

Speaker: Dr. Tero-Pekka Alastalo

Webinars

Current Challenges and Future Directions in Genetic Variant Interpretation

Date: 17 Jul, 2017

Time: 12:00 pm - 13:00 pm PDT

Duration: 54:01

C.E.U: -

Speaker: Jennifer Schleit

Webinars

Challenges in selecting the optimal genetic test for my patient

Date: 17 Jul, 2017

Time: 12:00 pm - 13:00 pm PDT

Duration: 54:01

C.E.U: -

Speaker: Dr. Tero-Pekka Alastalo

Webinars

New Standards in Genetic Interpretation with Next Generation Phenotyping

Date: 10 Jul, 2017

Time: 12:00 pm - 13:00 pm PDT

Duration: 46:45

C.E.U: -

Speaker: Peter Krawitz, Sara Reilly

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Upcoming webinars

Inborn Errors of Immunity: The Growing Role of Genetics

Past webinars

Keeping Pace: The Importance of a Shared Care Approach to Inherited Cardiovascular Disease

Introducing an open access genetic testing program for patients with inherited retinal degeneration

Genetic Testing for Individuals with Kidney Disease: Updates and Clinical Utility

How to solve challenging cases? Part II

Behind the scenes: What it actually takes to make a genetic test

Talk: Emerging opportunities in resolving difficult-to-sequence regions – PKD1 as a case example

Talk: High resolution CNV detection – a powerful diagnostic tool

How to solve challenging cases? Part I

What if it’s a variant of uncertain significance (VUS)?

Talk: Improved Diagnostic Yield in Rare Hereditary Disorders - Meeting Clinical Needs Using Customized Whole Exome Sequencing Solutions

High quality genetic diagnostics of polycystic kidney disease with NGS technology

Genetic Testing to enhance the value of a patient registry – A case study in the Inherited Retinal Dystrophies

Getting the most from exomes

Shedding light on complex regions in genetics

Utility of genetic testing and application to immune-related disorders

Nucleus – Faster and easier access to ordering genetic testing for your patient

Raising the bar: What to expect from cardiovascular genetic testing in 2018

Understanding Variants of Uncertain Significance

Genetic Diagnostics and Targeted Therapies of Primary Immunodeficiency Diseases (PID)

Utilization of NGS in Genetic Diagnostics of Inherited Retinal Diseases with Panel Update

Current Challenges and Future Directions in Genetic Variant Interpretation

Challenges in selecting the optimal genetic test for my patient

New Standards in Genetic Interpretation with Next Generation Phenotyping

Subscribe to our newsletter

Talk: Improved Diagnostic Yield in Rare Hereditary Disorders -Meeting Clinical Needs Using Customized Whole Exome Sequencing Solutions