Fantastic work!! We are all excited with the results for this patient. Can you imagine that so far three laboratories (Harvard, Toronto and Munich) have analysed DNA (WES ) with negative results. I suppose that the deletion could not be detected by SEQUENCING. We are grateful to you and your lab for your contribution to the diagnosis of this puzzling case. Of course we will share our experience with your company.
Dr. Dimitra Lianou, University of Athens, Greece, November 2018
"Coordinating Centre for Children’s Rare Diseases Children‘s hospital, Vilnius University Hospital Santaros Clinics in Lithuania has been working with CENTOGENE laboratory for over 5 years. They are a helpful and trustworthy partner. About 400 children with rare diseases visit Children’s Hospital yearly and most of them require genetic testing. Thanks to CENTOGENE, we have managed to diagnose many children and adults, discover new mutations and genotype – phenotype correlations. Correct diagnoses have helped in prescribing effective treatments and setting up individualized care plans.
CENTOGENE employees are high quality specialists and their professional description and interpretation of test results are a great help to physicians, their response is fast and well structured. Services provided are also excellent: physicians gain access to a database where all their tests results can be checked; there is an alert system that notifies about new results; it is also possible to ask for a specialist clarification if there are any questions about the results. CENTOGENE webinars are also very enjoyable. Their website provides many answers about rare diseases and a database on current genetic tests. We are happy to work together in multicenter studies such as BioAlport, Lysoprove, TuScCom.
CENTOGENE system works very well and I would recommend their laboratory to all specialists treating children and adults with rare diseases."
Prof. Rimante Cerkauskiene, MD,PhD
Coordinating centre for Children's rare diseases, Vilnius University Hospital Santaros clinics, Lithuania October 2018
Dear CENTOGENE team,
I would like to express my deepest appreciation to CENTOGENE Laboratory and all those who provided the possibility to sucesfully work together since two years. A special gratitude I give to our collaborator and dearest friend Professor Rolfs, whose contribution has been outstanding and continously stimulating helping us to coordinate the projects especially in feeding us with exiting scientific finding in our field of work, which is Rare Diseases.
A special thanks goes to the team, who helped us with each step of testing procedures by facilitating it and being always ready to give their comment and advices.
It takes huge effort in countries like ours to make possible what we have achieved in those two years, but how wonderful we have such collaboratiors who made available for the first time in Albania genetic testing for Rare Diseases.
Thanks to CENTOGENE Laboratory our Rare Disease Center has helped many albanian families who have their beloved dignosed with Gaucher disease and in extreme financial dificulties by covering all costs fo diagnostic and biomarkers on regular bases testing.
I must proudly emphasize that we are one of few centers monitoring our Gaucher patients under ERT treatment by quantification of Lyso Gb1 levels, which is a direct and extraordinary contribution of Professor Rolfs scientific work. Lyso Gb1 quantification is helping us to evaluate the efficacy of ERT and better individualize the treatment.
I look forward to seeing what comes in the future and hope to expand our sucessful collaboration with CENTOGENE Laboratory.
What a priviledge it is to be a part of such an amazing collaborative enviroinement, filled with such amazing people!
Prof. Paskal Cullufe,
UHC "Mother Teresa", Tirana, Albania October 2018
On behalf of Dr. Horovitz and the entire Department of Clinical Genetics team at Instituto Fernandes Figueira, Brazil, we thank CENTOGENE for the CentoDx® offered to our patient so kindly and free of charge. We are pleased with the diagnosis since we can adjust the patients diet properly and hopefully improve her outcome and prognosis.
On addition, thank you for releasing the report in Portuguese, since it will be easier for the family's genetic counselling (they don't speak English).
Laila Gallo, Clinical Genetics team
Instituto Fernandes Figueira, Brazil, October 2018
As a busy academic neurogeneticist, I want the best, most accurate and fastest diagnostic services for the anxious families I encounter, who are searching for difficult answers. For more than 6 years, CENTOGENE has provided outstanding diagnostic and clinical services for the AUBMC Special Kids Clinic. Thanks to their stellar work, many future affected pregnancies averted and early therapy and support services secured for a great number of children.
What I value the most is that there are consummate and caring scientists and geneticists at the other end, always available for questions and providing immediate answers. Nothing would make me happier than to see the incidence of neurogenetic disorders go down drastically….but….until then…I am grateful to have access to state of the art diagnostics with CENTOGENE by my side!
Prof. Rose-Mary Boustany, MD
American University of Beirut, Lebanon, October 2018
I have had a personal experience with CENTOGENE AG for a few years, and I have been really amazed how wonderfully organized their system is and how fast they are. Their work so much helped me and my patients to deal with their genetic conditions in terms of genetic counseling and treatment. More importantly, they are so much dedicated to genetic disease research!
Prof. Beom Hee Lee, MD,PhD
University of Ulsan College of Medicine, South Korea, October 2018
I, Prof. Laila Selim, Cairo university children hospital, worked with CENTOGENE team in the project entitled: biomarkers in lysosomal storage diseases: an international, multicenter study, from February 2015 till the present time and our collaboration is still ongoing. Through my work with the CENTOGENE team, I was able to diagnose hundreds of patients with different LSDs diseases. Also, CENTOGENE in a trial to improve the clinical reports, perform clinical CentoXome® which has resulted in increasing the diagnostic yield for many patients for whom testing for the requested genes was negative. Also, accepting some patients on the charity program helped to reach the diagnosis and to perform a proper genetic counseling for these families. The CENTOGENE team led by Prof Rolfs is really a wonderful and extremely cooperative team and I am so glad to continue collaboration with them.
Prof. Laila Selim, MD, PhD
Cairo University Children Hospital, October 2018
Dear Prof. Rolfs,
I want to thank you again for your support in our activity in rare disease field in Romania. It was a great meeting at Rare Disease Day symposium in Bucharest on 23th February. CENTOGENE team participation contributed immensely to our event. It's amazing how much value you offered to our specialists looking to learn about rare diseases and new genomic technologies. They were incredible excited about the progress your team have made. I would like to express my sincere appreciation for your time and your help for our patients with rare unknown conditions even through supporting some genetic tests using genomic technologies. And my patients' families want to thank you for all your efforts to diagnose their rare conditions.
I want to invite you to continue to share your expertise with us. Thank you again for all!
Dr. Vasilica Plaiasu, INSMC "Alessandrescu-Rusescu“ Children Hospital,
Bucharest, Romania, March 2017
Dear colleagues, the world's best laboratory CENTOGENE!
The team UIKG and KhSMGC wishes you a Happy New Year and Merry Christmas!
We wish you prosperity, the luckiest year - 2017, good health, peace, prosperity, harmony and joy of life!
Prof. Elena Grechanina, Kharkov Specialized Medical Genetic Centre, Kharkov,
Ukraine, December 2016
Congratulation for this success. The secret key of such achievement is the continuous unlimited help, collaboration, dedication and hard work from CENTOGENE team. Special thanks to Daniel and Rami. Looking forward for more publications togother in the near future.
(note of CENTOGENE: reference is the joint publication Trujillano et. al. Clinical exome sequencing: results from 2819 samples reflecting 1000 families. EJHG 2016)
Majid Alfadhel MD, MHSc, SSC-Ped, ABHS(CH), FCCMG Head Genetics Division, Department of Pediatrics Associate Professor, King Saud bin Abdulaziz University for Health Sciences (KSAU-HS) King Abdulaziz Medical City Riyadh
Riyadh, November 2016
Thank you very much for your unlimited help and support."
Saudi-Arabia, December 2015
"I received your letter, read it thoroughly and enjoyed. After that, I took a look at your site which was fantastic for me and gained a lot of information. My major is Medical Biotechnology. So, I will be happy to be able to work with you."
Iran, December 2015
“Thank you very much for the result in the name of the family. Your very fast response is highly appreciated.”
Dubai, December 2015
I really appreciate your excellent efforts.
Doha-Qatar, November 2015
Bravo to you and your team for the spectacular effort in getting this report against a looming deadline.
My warmest thanks to all.
Dr. Willie Reardon, Consultant Clinical Geneticist, Our Lady's Hospital for Sick Children, Dublin, Ireland
I am writing to thank you for the extended testing you provided for our patient.
We did not think of repeating the sequencing of the same gene before, since it was performed in a well-established laboratory. With your results, we will be able to plan for a prenatal with confidence.
Turkey, November 2015
"Speaking on behalf of my group, we enjoy and very much value the service your lab provides and plan to do so going forward. Thank you for all that you do!"
US, November 2015
"Thank you very much indeed for your fast and professional service. We greatly appreciate it. I am glad there is such an organisation as yourself."
Turkey, November 2015
„I would like to congratulate you and your team for the exome report on my patient. This was a very puzzling case and the patient had seen many doctors. I am very happy that CENTOGENE was able to identify the mutation. Since its present in father and daughter who are symptomatic and not in the mother would tend to support that it is pathogenic.
Please convey my congratulations and thanks to your staff.“
Dr. I. C. Verma, Sir Ganga Ram Hospital, India, November 2015
"Thank you so much for your help and quick response."
US, October 2015
"As always I was very happy with the service provided by CENTOGENE."
Australia, January 2015
"Every time, in any situation you help & guide me, even by cell phone, I thank & appreciate it so much."
Iran, January 2015
"This was a most comprehensive and prompt response to a question that I only asked yesterday. Thank you so much. I am very impressed and grateful."
South Africa, September 2014
"So far I sent one question through the site and got a prompt answer, not even 48 hours. Very nice! Thank you."
Georgia, August 2014
"Thank you so much for your reply! My life just got a little bit easier..."
Stockholm, Sweden, June 2014
"I appreciate very much your excellent kind of service, accuracy and your active team was very cooperative helping in diagnosis of our patients and offering hope to them. Thank you so much."
Cairo, Egypt, May 2014
"Your lab identified a BRCA2 mutation and she is fortunate enough now to have preventative options offered to her. I truly appreciated your help in this case."
Doha, Qatar, April 2014
"We used your services and found it at high level and very professional. We also found your filtercards very easy to use."
Rome, Italy, February 2014
"The patient, the family and me are very grateful with you and your lab that fill our hopes with your excellent services, both from the point of view of high-quality, scientific support and human values in this case. We are grateful for the time given, excellent communication, great understanding, sympathy and solidarity. THANK YOU!"
La Paz, Bolivia, January 2014
"A huge thank you to you and your wonderful team for getting this to me today. I look forward to working with you again soon"
Canada, January 2014
"As always I was very happy with the service provided by CENTOGENE."
Sydney, Australia, January 2014
"CENTOGENE has provided a good service, as this is pretty rapid in terms of genetic tests (single gene analysis). They have been splendid."
Brisbane, Australia, January 2014
"I started using Cento a few months ago and am very satisfied with your services: prompt response and excellent turnaround time and full service. Keep up the good work."
Beirut, Lebanon, January 2014
"Keep up the good work"
India, January 2014