News & Announcements

March 23rd, 2017

Impact Genetics Launches BAP1 Tumor Predisposition Syndrome (BAP1-TPDS) Genetic Test.

Mutations in BAP1 cause a novel cancer syndrome which is characterized by early age onset of
benign melanocytic skin tumors, and later in life by a high incidence of mesothelioma, uveal melanoma,
cutaneous melanoma, renal cell carcinoma and additional cancers.

Now available:

– Full BAP1 gene sequencing, copy number assessment and expert reporting
and interpretation.

– Comprehensive pre-test and/or post-test genetic counseling, provided by LabCorp
Integrated Genetics, using telegenetics

BAP1-TPDS can be ordered in combination with Impact Genetic’s Uveal Melanoma
Prognostic Genetic Test

Screening guidelines:

Rai K, Pilarkski R, Cibulla CM, Abdel-Rahman MH. Comprehensive review of BAP1 tumor predisposition syndrome with report of two new cases. Clin. Genet. 2016; 89: 285-94.

For additional information please contact us at 1-877-624-9769 or info@impactgenetics.com


March 20th, 2017

See you at ISOO 2017

Impact Genetics looks forward to seeing you at the 18th biennial International Society of Ocular Oncology
meeting in Sydney, Australia
.

Dr. Hilary Racher and Ms. Jaime Jessen will be presenting 2 Short Case and 2 Free Paper Oral Presentations.

 

Jaime Jessen, Bsc, MSc, CGC, CCGC

Jaime Jessen, BSc, MSc, CGC, CCGC
jjessen@impactgenetics.com

Dr. Hilary Racher, PhD, FCCMG, DABMGG

Dr. Hilary Racher, PhD, FCCMG, DABMGG
hracher@impactgenetics.com

Saturday, March 25, 2017 4:00 pm

Review of the distribution of DNA alterations identified by our uveal melanoma (UM) prognostic assay

Jaime Jessen, BSc, MSc, CGC, CCGC

Sunday, March 26, 2017 10:30 am

Telephone (early) versus examination (late) disclosure of prognostic uveal melanoma results: Associations with anxiety and depression

Jaime Jessen, BSc, MSc, CGC, CCGC

Sunday, March 26, 2017 5:10 pm

Using droplet digital polymerase chain reaction (ddPCR) to confirm and validate copy number variants (CNVs) and low level mosaic single nucleotide variants (SNV) identified from RB1 next generation sequencing (NGS)

Dr. Hilary Racher, PhD, FCCMG, DABMG

Monday, March 27, 2017 3:30 pm

RB1 cDNA mutation screening in a hereditary case of unilateral retinoblastoma reveals aberrant mRNA splicing and facilitates detection of a deep intronic substitution

Dr. Hilary Racher, PhD, FCCMG, DABMGG


March 16th, 2017

Now Available: Faster test turn around times, updated and improved test order forms

Productivity and efficiency can be achieved only step by step with sustained hard work, relentless attention to details and insistence on the highest standards of quality and performance.
– J. R. D. Tata

At Impact Genetics we strive to continuously improve our service and test quality. We are excited to announce that our trusted gold standard molecular analysis and interpretation is faster than ever before.

UPDATED Test Turn Around Times

Retinoblastoma Genetic Test
Proband…………………………………………………………………………………………… 4 to 6 weeks
Known Familial Mutation……………………………………………………………………….. 2 to 3 weeks
Prenatal…………………………………………………………………………………………… 7 working days

Hereditary Hemorrhagic Telangiectasia (HHT) Genetic Test
Proband…………………………………………………………………………………………… 6 to 9 weeks
Known Familial Mutation……………………………………………………………………….. 2 to 3 weeks

Uveal Melanoma Prognostic Genetic Test
Impact Genetics UM Prognostic Test………………………………………………………….. 3 to 6 weeks

UPDATED Forms

Newly update and improved individual forms and test submission packages are available in the Order a Test section of the website.

For additional information please contact us at 1-877-624-9769 or at info@impactgenetics.com.


February 22nd, 2017

Research Brings Hope to People Living with a Rare Disease

Researchers and families fighting rare Diseases together

Tuesday February 28th, 2017 6:30pm – 8:30pm

The Hospital for Sick Children
Peter Gilgan Research and Learning Tower Auditorium
686 Bay Street, Toronto
Ontario, Canada

Speaker: Meryl Acker BScH, MSc
Research impacts medical management in hereditary cancer predisposition

Speaker: Erica Spencer
Patient voice in hereditary cancer

Doors open at 6:30pm
Children Welcome
RSVP: torontofamilies@rarediseasefoundation.org

Reception to follow

*This event is independent from Impact Genetics.


February 13th, 2017

Uveal Melanoma Prognostic Genetic Test will now include SF3B1, EIF1AX, GNAQ and GNA11 sequencing for tumor confirmation in chromosomally normal tumor samples.

Impact Genetics has added two additional genes to our uveal melonoma tumor analysis SF3B1 and EIF1AX.

Recent publications (Yavuzyigitogly et al 2016 PMID: 26923342; Royer-Bertrand et al 2016 PMID: 27745836; Van Beek et al 2015 PMID: 26086698) have shown that disomy 3 patients with SF3B1 mutation are at increased risk to develop late-onset metastases, often presenting more than 5 years after diagnosis.

For disomy 3 samples that show normal MLPA and MSA results, mutation analysis will be performed on any remaining DNA.

SF3B1 will be preferentially reported allowing both tumor confirmation and enhanced prognostication for this unique patient group.

Coming Soon

– Impact Genetics will offer a 5 gene uveal melanoma tumor panel; GNAQ, GNA11, SF3B1, EIF1AX and BAP1.
This will be orderable regardless of prognostic test result (tumor chromosomal status).

– Impact Genetics will offer BAP1 tumor predisposition syndrome germline (hereditary) analysis and genetic counseling services.

For additional information please contact us at 1-877-624-9769 or at info@impactgenetics.com.


February 13th, 2017

Important Shipping Notice for the Family Day Holiday, Monday February 20th, 2017.

Monday February 20th 2017 is Family Day in Ontario Canada, a statutory holiday. Our laboratory and offices will be closed, and not be receiving samples.

We request that cell culture or prenatal samples are shipped to be delivered on or before Friday February 17th; or on Tuesday February 21st and after.

Regular hours for receiving samples resumes on Tuesday February 21st, 2017.

Please contact us directly with any questions you may have at 1-877-624-9769 or at info@impactgenetics.com.


December 22nd, 2016


November 20th, 2016

Genetic Counseling Awareness Week

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Happy Genetic Counselling Awareness Week! Today marks the beginning of the 7th annual Genetic Counselling Awareness Week. This year’s theme is “Genetic Conditions: Not as Rare As You May Think”.

From November 20th to 26th, 2016, the Canadian Association of Genetic Counsellors (CAGC) is hosting Genetic Counselling Awareness Week and will be hosting events across Canada.

Genetic counsellors help people understand and adapt to complicated health-related information in a genetics setting. They can help individuals and families with rare genetic disorders in many ways, from providing support during the genetic testing process and explaining the complexities of genetic test results and diagnoses, to helping determine how newly discovered genes can be used in genetic testing. For genetic counsellors, rare may be unique, but it is not uncommon. This year, Genetic Counselling Awareness Week will focus on the idea that genetic conditions are more common than many may believe.
– Canadian Association of Genetic Counsellors

To learn more about Genetic Counselling Awareness Week, visit the CAGC’s Facebook page or follow them on Twitter @CAGC_ACCG.


November 18th, 2016

Important Shipping Notice for the 2016 / 2017 Holiday Season

Happy Holidays!

Our laboratory and offices will be closed for the Holidays and not be receiving samples on the following days:

Monday December 26th, 2016
Tuesday December 27th, 2016
Monday January 2nd, 2017

We request that cell culture or prenatal samples are shipped to be delivered on or before Friday December 23rd or from Wednesday December 28th to Friday December 30th.

Regular hours for receiving samples will resume on Tuesday January 3rd, 2017.

Please contact us directly with any questions you may have at 1-877-624-9769 or at info@impactgenetics.com.


April 4th, 2016

Impact Genetics Tests Listed on LabCorp Test Menu.

April 4th, 2016 – Impact Genetics’ uveal melanoma and HHT tests are now available to be ordered through LabCorp. Customers in the United States can now send samples to Impact Genetics through LabCorp, improving access in larger institutions and in some cases, improving insurance coverage. LabCorp will handle specimen transport, insurance prior-authorizations and billing.

Contact us for details about the process.


May 28th, 2014

Impact Genetics Launches New Test for Uveal Melanoma.

May 28th, 2014 – Impact Genetics will launch a prognostic test for Uveal Melanoma on June 4th, 2014. This genetic test will identify risk of metastasis, indicating survival prognosis in patients with Uveal Melanoma.

“Prognostication may contribute to patient management, possibly encouraging a more aggressive approach if the tumor shows lethal genetic abnormalities”, says Dr. Bertil Damato, medical advisor to Impact Genetics and Director of the Ocular Oncology Service and Professor of Ophthalmology and Radiation Oncology, University of California, San Francisco.

“Prognostic tests identify patients at higher metastatic risk, who may benefit from the ongoing clinical trials for therapies of early metastases, and can also favourably impact the economics of metastatic surveillance”, says Dr. Hatem Krema, Director of the Ocular Oncology Service, University of Toronto, Canada.

For more information see our Uveal Melanoma Test Description:


February 17th, 2014

Impact Genetics relocates to Bowmanville.

February 17, 2014 – NEW SHIPPING ADDRESS, please notify us of all shipments ahead of time. Impact Genetics is relocating all operations to our new Genetics Centre of Excellence in Bowmanville, Ontario. Bowmanville is on the east side of the Greater Toronto Area. The expanded space is an exciting environment for our growing team and will enable development of new services. The full Impact team will move with us.

Please use our new shipping address below for all shipments starting today.

New Shipping Address:

Impact Genetics Inc.
1100 Bennett Road – Unit 4
Bowmanville, ON L1C 3K5
CANADA

Contact us with any questions.


October 3rd, 2013

Gamma-Dynacare Medical Laboratories Announces Acquisition of Controlling Interest in Impact Genetics.

October 3, 2013 – Gamma-Dynacare has acquired a controlling interest in Impact Genetics, helping to support our expanding mission of providing cost-effective, high quality genetic testing for rare diseases. Our team will remain in place and Dr. Gallie continues in her role of Medical Director for Retinoblastoma.

Learn more about this announcement and our company.

Read the full press release


July 17th, 2013

Impact Genetics’ Retinoblastoma Genetic Test now Includes the MYCN Gene.

Just published in The Lancet Oncology (Characterisation of retinoblastomas without RB1 mutations), copy number changes in the MYCN gene cause about 2% of unilateral retinoblastoma. In those cases, the RB1 gene is normal. At Impact, we now test MYCN copy number where appropriate. Patients with this form of non-heritable retinoblastoma have aggressive cancer, but a much better genetic prognosis.

Please see our retinoblastoma genetic test description for more information.


March 14th, 2013

New Form of Retinoblastoma Identified by our Team Members

Characterisation of retinoblastomas without RB1 mutations.
Published in The Lancet Oncology, Volume 14, Issue 4, Pages 327 – 334, April 2013

Retinoblastoma is the childhood retinal cancer that defined tumour-suppressor genes. Previous work shows that mutation of both alleles of the RB1 retinoblastoma suppressor gene initiates disease. This study characterizes non-familial retinoblastoma tumours with no detectable RB1 mutations.

Impact is proud of it’s team for making this important discovery, which was only possible by our open global collaborations and high volume of research consented RB clinical tests.

Read the full paper online at Lancet Oncology

Media coverage;


March 12th, 2013

Impact Genetics Introduces Retinoblastoma Online “Webinar” Education Series

Our new educational webinar aims to share information about how to improve outcomes for retinoblastoma patients through optimal use of genetic knowledge. Join one of our regularly scheduled webinars to learn more about genetics of retinoblastoma including new discoveries, patients and families that benefit from genetic testing using case examples and the medical necessity, costs and cost benefits. Check for the latest dates