PODCAST

Genetics

ReachMD

science & medicine medicine

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00:00:00

Genetics in Psoriasis: Impacts on Risk,...

Genetics ·

2025/07/23

Guest: Audrey Bui, DO Genetic insights are reshaping how we understand the development and comorbidities of psoriasis, as well as treatment response in patients. Hear Dr. Audrey Bui discuss how genetic variants influence risks for certain conditions, how they may predict response to therapies like methotrexate, ustekinumab, and IL-17 inhibitors, and how integrating genetic markers into clinical care can enable more targeted, effective psoriasis management. Dr. Bui is a recent graduate

00:00:00

Newborn Gene Sequencing: Expanding Early Detection of...

Genetics ·

2025/04/14

Guest: Jordan Orange, MD, PhD Guest: Joshua Milner, MD Guest: Eric Silver, MD Guest: Steven Lobritto, MD On this episode of Advances in Care, host Erin Welsh explores the story behind the GUARDIAN study, where thousands of newborn babies have been screened against rare disease by sequencing their genes, and looking for more conditions than any of the current standard screening panels. First, she hears from Dr. Jordan Orange, Physician-in-Chief at Morgan Stanley Children’s

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The Impact of RADIANT: A Deep Dive into the Study

Genetics ·

2023/09/20

Host: John Buse, MD, PhD Guest: Louis Philipson, MD, PhD Over the last 15 years, the monogenic diabetes registry now has over 4,000 patients involved, and from that, the RADIANT study was started to identify new kinds of rare and atypical diabetes. So how can genetics testing and the RADIANT study provide atypical diabetes patients with better diagnoses and treatment? Learn more with Dr. John Buse and Dr. Louis Philipson, Professor in the Department of Medicine and Pediatrics at

00:00:00

Uncovering Disease Progression in Multiple Sclerosis

Genetics ·

2023/08/13

Guest: Sergio Baranzini, PhD A recent study was designed by the International Multiple Sclerosis Genetics Consortium with the goal in mind to find out whether the severity of multiple sclerosis (MS) could be influenced by genetics. Dive in with Dr. Sergio Baranzini, Distinguished Professor of Neurology at the University of California San Fransico and Co-Senior Author of the study.

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Living with Lymphedema: A Patient Perspective

Genetics ·

2021/04/07

Host: Hector O. Chapa, MD, FACOG Guest: Cameron Ayala Hundreds of millions of people worldwide suffer from lymphedema and lymphatic diseases. Joining us to provide a personal perspective on this condition is Cameron Ayala, a former reality TV persona, compression specialist, and lymphedema patient who will be sharing his experience with Dr. Hector Chapa.

00:00:00

Exploring EGFR Mutations in Lung Cancer: Key...

Genetics ·

2021/03/18

Host: Jacob Sands, MD Guest: Pasi Antero Jänne, MD, PhD Once we’ve confirmed a patient has EGFR-mutated lung cancer, how can we treat them? Joining Dr. Jacob Sands to discuss the current and future treatments for this mutation is Dr. Pasi Janne, a translational thoracic medical oncologist at the Dana-Farber Cancer Institute.

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Exploring Stem Cell Research & Novel Options in Type...

Genetics ·

2021/03/09

Host: John E. Anderson, MD Guest: Matthias Hebrok, PhD Emerging research may offer clinicians an alternative approach to treating type 1 diabetes. Dr. John Anderson meets with Dr. Matthias Hebrok, a professor in diabetes research and director of the Diabetes Center at the University of California, San Francisco, to discuss his groundbreaking research on insulin-producing stem cells.

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Gaining a Deeper Understanding of Inherited...

Genetics ·

2020/06/10

Host: Jennifer Caudle, DO Guest: Anjali Owens, MD Without any targeted therapies available for inherited cardiomyopathy, how can we treat our patients coping with its debilitating symptoms? Here to share her diagnostic and management strategies along with key data from a recent study is Dr. Anjali Owens, Medical Director at the Center for Inherited Heart Disease at Penn Medicine.

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Analyzing the Available Treatments for...

Genetics ·

2020/04/20

Host: Paul Doghramji, MD Guest: Maria Escolar, MD, MS Adrenoleukodystrophy (ALD) is a rare genetic disorder that when left untreated, can have severe and even fatal consequences. Here to review the available treatment options for these patients is Dr. Maria Escolar, the Director of the Program for the Study of Neurodevelopment in Rare Disorders and a Professor of Pediatrics at the University of Pittsburgh School of Medicine.

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FDA’s Pursuit in Progressing Gene Therapy While...

Genetics ·

2020/03/27

Host: Linda Bernstein, Pharm.D. There are currently four gene therapy products approved by the FDA, and with the FDA anticipating that there will be many more approvals in the future, how can they continue advancing the field of gene therapy all while ensuring that these innovative products meet their strict standards for safety and effectiveness? Pharmacist Dr. Linda Bernstein breaks down their six new guidance documents.

00:00:00

Keys to Avoiding an Adrenoleukodystrophy Misdiagnosis

Genetics ·

2020/02/06

Host: Mario R. Nacinovich, Jr., MSc Guest: Paul Orchard, MD Although it only affects about one in 18,000 people, the impacts of adrenoleukodystrophy cannot be underestimated. That’s why Dr. Paul Orchard joins Mario Nacinovich to talk about this rare—and fatal—genetic disease, why it’s often underdiagnosed and confused with other conditions, and how we can treat it once we’ve reached an accurate diagnosis.

00:00:00

FDA-Approved Gene Therapy Reverses Blindness in...

Genetics ·

2018/04/23

Host: Jennifer Caudle, DO Guest: Jean Bennett, MD, PhD Guest: Albert Maguire, MD Power couple Drs. Jean Bennett and Albert Maguire discuss how their new therapy for the RPE65 gene, which causes retinal blindness, was recently approved by the FDA to become the first gene therapy treatment for a genetic disease in the United States and the first worldwide treatment for inherited blindness. Not only do they delve into the mechanics of the corrected gene injection, but they also

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Autism Spectrum Disorder Risk Factors: Environmental...

Genetics ·

2017/11/17

Host: Paul Rokuskie Scientists have been doing research into many areas of autism spectrum disorder in the hopes of explaining the doubling of its prevalence rate over the past decade. Both environmental risk factors and genetic components are areas of intense scrutiny for researchers seeking to understand the root causes of autism. Host Paul Rokuskie talks with Craig Newschaffer, Professor, Associate Dean for Research, and Director of the A.J. Drexel Autism Institute, about the risk

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CAR-T Cell Therapy: A Breakthrough Treatment for...

Genetics ·

2017/10/23

Host: Shira Johnson, MD Guest: Robert Vonderheide, MD For years, the foundations of cancer treatment, surgery, chemotherapy, and radiation therapy were utilized with the objective of weakening cancer. But over the past several years, immunotherapy – therapies that enlist and strengthen the power of a patient’s immune system to attack tumors - has emerged as a new tool for fighting cancer. In August 2017, one such treatment approach, called Chimeric Antigen Receptor or CAR T-cell

00:00:00

Curing Blindness: How Researchers are Utilizing Gene...

Genetics ·

2017/01/05

Host: Shira Johnson, MD Guest: Jean Bennett, MD, PhD There are 39 million people worldwide who are in total blindness and another 246 million with very low vision. The most frequent forms of visual impairment are caused by problems that can be corrected. Dr. Shira Johnson welcomes Dr. Jean Bennett, Professor of Ophthalmology and Cell and Developmental Biology at the University of Pennsylvania and researcher at the Children’s Hospital of Philadelphia. Dr. Bennett discusses her

00:00:00

Pharmacometabolomics to Predict Statin Response:...

Genetics ·

2016/10/03

Host: Alan S. Brown, MD, FACC, FAHA, FNLA Live from the Clinical Lipid Update of the National Lipid Association in Amelia Island, FL, host Dr. Alan Brown welcomes Dr. Rhoda Cooper-DeHoff. Dr. Cooper-DeHoff is an Associate Professor in the Department of Pharmacotherapy and Translational Research and Division of Cardiovascular Medicine of the Colleges of Pharmacy and Medicine at the University of Florida. She is also Associate Director of the Center for Pharmacogenomics at this

00:00:00

Translational Genomics and Health Outcomes Research:...

Genetics ·

2015/02/16

Host: Howard Levy, MD, PhD Guest: Robert C Green, MD, MPH Genomic Medicine is making a rapid entry into the healthcare landscape, but questions on the potential vs realized impacts toward clinical care outcomes persist. Which genomic information will be crucial to patient care? Addressing this and other questions with host Dr. Howard Levy is Dr. Robert Green, Director of the Genes-2-People (G2P) Research Program in Translational Genomics and Health Outcomes at Brigham and Women's

00:00:00

The Role of the ASHG in Health Professional Education

Genetics ·

2015/02/16

Guest: Joseph D. McInerney, MA, MS Host: Howard Levy, MD, PhD Dr. Howard Levy welcomes Joseph McInerney, Executive Vice President of the American Society of Human Genetics, to talk about collaborative efforts within the Society to help healthcare professionals integrate genetics into clinical care for their patients and promote medical education for the wider public.

00:00:00

The Future of Clinical Sequencing: Whole Genome vs...

Genetics ·

2015/02/16

Guest: Richard Gibbs, PhD Host: Robert C Green, MD, MPH When patients and clinicians alike consider genome sequencing, an attitude of "more is better" often predominates notions of what information to obtain. But new perspectives on the comparative value and contained costs of more refined exome sequencing have since emerged. Joining host Dr. Robert Green to discuss the benefits and drawbacks of respective clinical sequencing options is Dr. Richard Gibbs, Wofford Cain Chair and

00:00:00

Ethical Issues in Genetic Testing: the Who, What,...

Genetics ·

2015/02/16

Guest: Wylie Burke, MD, PhD Host: Howard Levy, MD, PhD The advances of genetic and genomic medicine within clinical practice enable more precisioned, predictive care decisions. But with these new capabilities and access points to patient information come new ethical challenges. Understanding which information will be clinically valuable, how and where that information should be stored, who can access it and why are just starting points for ethical consideration. Joining Dr. Howard

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Genetics

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