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ACMG Foundation for Genetic and Genomic Medicine Elects Four Highly Accomplished Medical Genetics Professionals to Its Board of Directors

ACMG Foundation for Genetic and Genomic Medicine Elects Four Highly Accomplished Medical Genetics Professionals to Its Board of Directors

ACMG 遺傳與基因組醫學基金會選出四位成就卓著的醫學遺傳學專家加入其董事會
PR Newswire ·  04/11 21:30

BETHESDA, Md., April 11, 2024 /PRNewswire/ -- The ACMG Foundation for Genetic and Genomic Medicine (ACMGF) announced today that Marilyn C. Jones, MD, FACMG; Harry Ostrer, MD, FACMG; Lisa G. Shaffer, PhD, FACMG and Katie Johansen Taber, PhD were elected to the Board of Directors of the ACMGF. The ACMG Foundation is a national nonprofit foundation dedicated to facilitating the integration of genetics and genomics into medical practice. The board members are active participants, serving as advocates for the ACMG Foundation and for advancing its policies and programs.

馬里蘭州貝塞斯達,2024年4月11日 /PRNewswire/ — ACMG遺傳與基因組醫學基金會(ACMGF)今天宣佈,FACMG醫學博士瑪麗蓮·瓊斯、FACMG醫學博士哈里·奧斯特爾、FACMG博士麗莎·謝弗博士和凱蒂·約翰森·泰伯博士當選爲ACMGF董事會成員。ACMG基金會是一個全國性的非營利基金會,致力於促進遺傳學和基因組學融入醫學實踐。董事會成員是積極的參與者,是ACMG基金會和推進其政策和計劃的倡導者。

ACMG Foundation President Nancy J. Mendelsohn, MD, FACMG said, "We are pleased to welcome these four new members to the ACMG Foundation Board of Directors. Individually and combined they bring a new perspective along with their individual deep expertise. We are grateful for their enthusiasm and willingness to serve our genetics and genomics community."

ACMG基金會主席、醫學博士南希·門德爾松說:“我們很高興歡迎這四位新成員加入ACMG基金會董事會。無論是個人還是結合,他們都帶來了新的視角以及他們個人的深厚專業知識。我們感謝他們爲我們的遺傳學和基因組學界服務的熱情和意願。”

Marilyn C. Jones, MD, FACMG

瑪麗蓮·瓊斯,我,面對

A Past President of the ACMG (2007-2009), Dr. Marilyn C. Jones is the Clinical Services Chief of the Genetics and Dysmorphology Division at Rady Children's Hospital in San Diego and a Distinguished Professor of Clinical Pediatrics at the UC San Diego School of Medicine. She has served as the Medical Director of the Helen Bernardy Center for Medically Fragile Children for more than 40 years. With expertise in providing detailed patient phenotyping to aid gene discovery, Dr. Jones's career has focused on identifying underlying causation among patients with cleft and craniofacial disorders. In 2020 she received the David Bixler Distinguished Scientist in Craniofacial Research Award from the Society for Craniofacial Genetics and Developmental Biology, as well as the David W. Smith Award for Excellence in Genetics and Birth Defects Education from the American Academy of Pediatrics.

瑪麗蓮·瓊斯博士曾任ACMG主席(2007-2009年),是聖地亞哥雷迪兒童醫院遺傳學和畸形學部的臨床服務主任,也是加州大學聖地亞哥分校醫學院臨床兒科傑出教授。她擔任海倫·伯納迪醫療脆弱兒童中心醫學主任已有40多年。憑藉在提供詳細的患者表型分析以幫助基因發現方面的專業知識,瓊斯博士的職業生涯側重於識別裂縫和顱面部疾病患者的潛在因果關係。2020年,她獲得了顱面遺傳學與發育生物學學會頒發的大衛·比克斯勒顱面研究傑出科學家獎,以及美國兒科學會頒發的大衛·史密斯遺傳學和出生缺陷教育卓越獎。

"I am honored for the opportunity to serve the ACMG again through participation in the Foundation Board of Directors. The Foundation provides many of the resources that help the College move forward its agenda to help both the public and its members," said Dr. Jones.

“我很榮幸有機會通過加入基金會董事會再次爲ACMG服務。該基金會提供了許多資源,幫助學院推進其議程,爲公衆及其成員提供幫助。” 瓊斯博士說。

Harry Ostrer, MD, FACMG

哈里·奧斯特爾,醫學博士,FACMG

Dr. Harry Ostrer is Professor of Pathology and Pediatrics at Albert Einstein College of Medicine. From 1990-2011, he was the Director of the Human Genetics Program at New York University Langone Medical Center. His academic focus is in studying the genetic basis for common and rare disorders and developing new functional genomic technologies. Dr. Ostrer is also a long-time investigator of the genetics of the Jewish people and Hispanic and Latino people. In 2007, he organized the Jewish HapMap Project, an international effort to understand origins, migration and disease predispositions by mapping and sequencing the genomes of Jewish people. At his start-up company, Morgan and Mendel Genomics, Dr. Ostrer advises about translating the findings of novel functional genomic discoveries into tests that can be used to identify people's risks for having cancer or for predicting cancer's response to therapy.

哈里·奧斯特爾博士是阿爾伯特·愛因斯坦醫學院病理學和兒科教授。1990年至2011年,他在紐約大學朗格尼醫學中心擔任人類遺傳學項目主任。他的學術重點是研究常見和罕見疾病的遺傳基礎,以及開發新的功能基因組技術。奧斯特爾博士還是猶太人以及西班牙裔和拉丁裔遺傳學的長期研究者。2007年,他組織了猶太人HapMap項目,這是一項國際項目,旨在通過繪製猶太人的基因組圖和測序來了解起源、遷徙和疾病易感性。在他的初創公司摩根和孟德爾基因組學,奧斯特爾博士建議將新的功能基因組發現的發現轉化爲可用於識別人們患癌症的風險或預測癌症對治療的反應。

"My professional career has been entwined with creating opportunities for others in medical genetics by training them, sometimes through training programs that I created. But part of passing the mantle of achieving 'better health through genetics' for everyone is to support even larger and scalable opportunities," said Dr. Ostrer. "I am delighted to have the means to do so by joining old and new friends on the Board of Directors of the American College of Medical Genetics Foundation, whose philanthropic mission is to fund new programs and research."

“我的職業生涯與通過培訓他人爲醫學遺傳學領域創造機會交織在一起,有時是通過我創建的培訓計劃。但是,推卸'通過遺傳學改善每個人的健康狀況'的任務的一部分是支持更大、更可擴展的機會,” 奧斯特爾博士說。“我很高興有辦法與新老朋友一起加入美國醫學遺傳學學會基金會董事會,該基金會的慈善使命是資助新的項目和研究。”

Lisa G. Shaffer, PhD, FACMG

麗莎·謝弗博士,FACMG

Dr. Lisa G. Shaffer is founder and the former CEO of Genetic Veterinary Sciences, Inc. (DBA Paw Print Genetics), a canine, feline and avian genetic testing company serving breeders, veterinarians and owners. The company was acquired in 2021. Prior to that enterprise, she was co-founder, President and CEO of Signature Genomic Laboratories, the first diagnostic laboratory to offer clinical microarray testing for children with developmental disabilities. The recipient of numerous accolades for her entrepreneurship and business savvy, Dr. Shaffer was previously a tenured Professor of Molecular and Human Genetics at Baylor College of Medicine (1991-2002) and in the School of Molecular Biosciences at Washington State University (2002-2008). Dr. Shaffer has authored more than 340 peer-reviewed medical papers and four books.

麗莎·謝弗博士是遺傳獸醫科學公司(DBA Paw Print Genetics)的創始人兼前首席執行官,該公司是一家爲育種者、獸醫和所有者提供服務的犬類、貓科動物和鳥類基因檢測公司。該公司於 2021 年被收購。在加入該企業之前,她是Signature Genomic Laboratories的聯合創始人、總裁兼首席執行官,該實驗室是第一個爲發育障礙兒童提供臨床微陣列測試的診斷實驗室。謝弗博士因其創業精神和商業頭腦而獲得無數榮譽,此前曾在貝勒醫學院擔任分子與人類遺傳學終身教授(1991-2002年)和華盛頓州立大學分子生物科學學院(2002-2008年)。謝弗博士撰寫了340多篇經過同行評審的醫學論文和四本書。

"I am very excited to be rejoining the ACMG Foundation Board of Directors and look forward to supporting the mission of the ACMG and helping to raise awareness of medical genetics and promote its achievements. Medical genetics touches every aspect of human health, and this is an exciting time to be a part of the Foundation," said Dr. Shaffer.

“我很高興能重新加入ACMG基金會董事會,並期待支持ACMG的使命,幫助提高人們對醫學遺傳學的認識並促進其成就。醫學遺傳學涉及人類健康的方方面面,現在是加入基金會的激動人心的時刻,” 謝弗博士說。

Katie Johansen Taber, PhD

凱蒂·約翰森·泰伯博士

As the Vice President of Clinical Product Research & Partnerships at Myriad Genetics, Dr. Katie Johansen Taber's focus is on developing evidence and advancing initiatives to improve access to genetic testing in the areas of women's health, oncology and mental health. She leads a team responsible for clinical evidence strategy, real-world evidence development, clinical trial conduct and scientific publications. Prior to her current position, Dr. Johansen Taber was Senior Director of Clinical Development at the company's Women's Health business unit. Before joining Myriad Genetics, she served at the American Medical Association (2006-2017), where her work centered on educating healthcare professionals about the clinical implementation of genomics and precision medicine, and on identifying and managing precision medicine policy issues. Dr. Johansen Taber has held numerous positions on advisory committees and boards, including a current appointment on the National Academy of Sciences, Engineering and Medicine Roundtable on Genomics and Precision Health.

作爲Myriad Genetics的臨床產品研究與合作伙伴關係副總裁,凱蒂·約翰森·泰伯博士的重點是開發證據,推進各項舉措,以改善女性健康、腫瘤學和心理健康領域獲得基因檢測的機會。她領導的團隊負責臨床證據策略、現實世界的證據開發、臨床試驗的實施和科學出版物。在擔任現任職務之前,約翰森·泰伯博士曾擔任公司女性健康業務部門的臨床開發高級董事。在加入Myriad Genetics之前,她曾在美國醫學會任職(2006-2017年),其工作重點是教育醫療保健專業人員了解基因組學和精準醫療的臨床實施,以及識別和管理精準醫療政策問題。約翰森·泰伯博士曾在顧問委員會和董事會中擔任過多個職務,包括目前被任命爲美國國家科學院、工程和醫學基因組學和精準健康圓桌會議的成員。

"I'm thrilled to be elected to the ACMG Foundation Board of Directors and I look forward to working together to improve access to genetic testing," said Dr. Johansen Taber. "The Foundation's focus on evidence-based guidelines development, education and advocacy are important initiatives in realizing the ability to provide genetics-informed care to all patients who need it."

約翰森·泰伯博士說:“我很高興當選爲ACMG基金會董事會成員,我期待共同努力改善獲得基因檢測的機會。”“基金會專注於循證指南的制定、教育和宣傳,是實現向所有有需要的患者提供基因信息護理的能力的重要舉措。”

ACMGF Also Announces New Board Position and Thanks Outgoing Board Members

ACMGF還宣佈了新的董事會職位並感謝離任的董事會成員

In addition, Brynn Levy, MSc. (Med), PhD, FACMG, who joined the ACMG Foundation Board of Directors in 2019, was named to the newly created officer position of President-Elect.

此外,Brynn Levy,理學碩士。(醫學),博士,FACMG於2019年加入ACMG基金會董事會,被任命爲新設立的候任總裁官一職。

The ACMG Foundation also thanked the following board members who recently completed their terms of service: Nasha Fitter, MBA; Evan Jones, MBA and, in particular, David A.H. Whiteman, MD, FAAP, FACMG, who joined the Foundation Board of Directors in 2014 and served admirably as its Vice President since 2017.

ACMG基金會還感謝最近完成任期的以下董事會成員:Nasha Fitter,工商管理碩士;埃文·瓊斯,工商管理碩士,特別是 FAAP、FACMG 醫學博士大衛·懷特曼,他於 2014 年加入基金會董事會,自 2017 年起擔任副總裁,令人欽佩。

A complete roster of the ACMG Foundation Board can be found at .

ACMG基金會董事會的完整名單可在以下網址找到。

About the ACMG Foundation for Genetic and Genomic Medicine

關於 ACMG 遺傳與基因組醫學基金會

The ACMG Foundation for Genetic and Genomic Medicine, a 501(c)(3) nonprofit organization, is a community of supporters and contributors who understand the importance of medical genetics and genomics in healthcare. Established in 1992, the ACMG Foundation supports the American College of Medical Genetics and Genomics (ACMG) mission to "translate genes into health." Through its work, the ACMG Foundation fosters charitable giving, promotes training opportunities to attract future medical geneticists and genetic counselors to the field, shares information about medical genetics and genomics, and sponsors important research. To learn more and support the ACMG Foundation mission to create "Better Health through Genetics" visit acmgfoundation.org.

ACMG遺傳與基因組醫學基金會是一家501(c)(3)非營利組織,是一個由支持者和捐款者組成的社區,他們了解醫學遺傳學和基因組學在醫療保健中的重要性。ACMG基金會成立於1992年,支持美國醫學遺傳學和基因組學會(ACMG)“將基因轉化爲健康” 的使命。通過其工作,ACMG基金會促進慈善捐贈,促進培訓機會以吸引未來的醫學遺傳學家和遺傳顧問進入該領域,分享有關醫學遺傳學和基因組學的信息,並贊助重要的研究。要了解更多信息並支持ACMG基金會創造 “通過遺傳學改善健康” 的使命,請訪問acmgfoundation.org。

Contact:
Kathy Moran, MBA
[email protected]

聯繫人:
凱西·莫蘭,工商管理碩士
[電子郵件保護]

SOURCE ACMG Foundation for Genetic and Genomic Medicine

來源 ACMG 遺傳與基因組醫學基金會

譯文內容由第三人軟體翻譯。


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