Consumer Genomic Testing in 2020 WG Feero et al, JAMA, March 19, 202-0

Main|Search|PHGKB






Last Posted: Mar 20, 2020

---

• Consumer Genomic Testing in 2020
  WG Feero et al, JAMA, March 19, 202-0
• Consumer genetic testing: expectation and reality
  Genomics Education Program, January 2020
• Direct-to-consumer testing: a clinician’s guide
  Genomics Education Program, January 2020
• Why DNA tests are suddenly unpopular
  R Molla, VOX, February 2020
• The Need to Improve the Clinical Utility of Direct-to-Consumer Genetic Tests Either Too Narrow or Too Broad
  MK Kilbride et al, JAMA, February 20, 2020
• Your DNA is a valuable asset, so why give it to ancestry websites for free?
  L Spinney, the Guardian, February 2020
• Genetic Ancestry Testing-What Is It and Why Is It Important
  LB Jorde et al, JAMA, February 14, 2020
• Lessons Learned from Direct-to-Consumer Genetic Testing.
  Petersen Lauren M et al. Clinics in laboratory medicine 2020 Mar 40(1) 83-92
• The Impact of Direct-to-Consumer Genetic Testing on Patient and Provider.
  Dinulos Mary Beth Palko et al. Clinics in laboratory medicine 2020 Mar 40(1) 61-67
• Genomics Education in the Era of Personal Genomics: Academic, Professional, and Public Considerations.
  Whitley Kiara V et al. International journal of molecular sciences 2020 Jan 21(3)

more

A newly developed capture-based sequencing panel for genomic assay of lung cancer. Im Sun-Wha et al. Genes & genomics 2020 May

Main|Search|PHGKB




Last Posted: May 26, 2020

---

• A newly developed capture-based sequencing panel for genomic assay of lung cancer.
  Im Sun-Wha et al. Genes & genomics 2020 May
• Challenges and opportunities of cfDNA analysis implementation in clinical practice: Perspective of the International Society of Liquid Biopsy (ISLB).
  Rolfo Christian et al. Critical reviews in oncology/hematology 2020 May 151102978
• Precision Medicine Exits the Hype Cycle and Enters into Productive Clinical Use.
  Schmidt Ryan J et al. Clinics in laboratory medicine 2020 Jun 40(2) ix-x
• Prognostic significance of immune cell populations identified by machine learning in colorectal cancer using routine hematoxylin & eosin stained sections.
  Väyrynen Juha P et al. Clinical cancer research : an official journal of the American Association for Cancer Research 2020 May
• Targeted Therapy for Non-Small Cell Lung Cancer.
  Noor Zorawar S et al. Seminars in respiratory and critical care medicine 2020 Jun 41(3) 409-434
• Information Sources Used by Oncologists to Understand Multi-marker Tumor Panel Tests for Cancer Patients.
  Buckenmaier Susan S et al. Journal of cancer education : the official journal of the American Association for Cancer Education 2020 May
• Personalized medicine in genetic epilepsies - possibilities, challenges, and new frontiers.
  Helbig Ingo et al. Neuropharmacology 2020 Jan 172107970
• The Impact of Whole Genome Data on Therapeutic Decision-Making in Metastatic Prostate Cancer: A Retrospective Analysis.
  Crumbaker Megan et al. Cancers 2020 May 12(5)
• From precision medicine to imprecision medicine through limited diagnostic ability to detect low allelic frequency mutations.
  Serrano María José et al. Translational lung cancer research 2020 Apr 9(2) 180-183
• Pharmacogenomic Testing to Guide Personalized Cancer Medicine Decisions in Private Oncology Practice: A Case Study.
  Astras George et al. Frontiers in oncology 2020 10521

more

All Hands on Deck! Geospatial Mapping in Outbreaks ATSDR, May 2020

Main|Search|PHGKB




Last Posted: May 13, 2020

---

• All Hands on Deck! Geospatial Mapping in Outbreaks
  ATSDR, May 2020
• Ethics and governance for digital disease surveillance
  MM Mello et al, Science, May 11, 2020
• Precision health: A pragmatic approach to understanding and addressing key factors in autoimmune diseases.
  Conrad Karsten et al. Autoimmunity reviews 2020 May 19(5) 102508
• Using Digital Technologies in Precision Public Health: COVID-19 and Beyond
  MJ Khoury et al, CDC Blog, April 2020
• The impact of genomics on precision public health
  Call for Papers, Genome Medicine, April 22, 2020
• The Public Health Impact of COVID-19: Why Host Genomics?
  MJ Khoury el al, CDC Blog, April 21, 2020
• Mapping local patterns of childhood overweight and wasting in low- and middle-income countries between 2000 and 2017
  Nature Medicine, April 20, 2020
• Aggregated mobility data could help fight COVID-19
  CO Buckee et al, Science, April 10, 2020
• Precision Medicine and Precision Public Health in the Era of Pathogen Next-Generation Sequencing.
  Leguia Mariana et al. The Journal of infectious diseases 2020 Mar (Supplement_3) S289-S291
• Addressing Social Determinants of Health- Time for a Polysocial Risk Score
  JF Figueroa et al, JAMA, April 3, 2020

more

Experience with Parent Follow-Up for Communication Outcomes after Newborn Screening Identifies Carrier Status. Farrell Michael H et al. The Journal of pediatrics 2020 May

Main|Search|PHGKB




Last Posted: May 14, 2020

---

• Experience with Parent Follow-Up for Communication Outcomes after Newborn Screening Identifies Carrier Status.
  Farrell Michael H et al. The Journal of pediatrics 2020 May
• Returning genomic results in a Federally Qualified Health Center: the intersection of precision medicine and social determinants of health.
  Shaibi Gabriel Q et al. Genetics in medicine : official journal of the American College of Medical Genetics 2020 May
• Proposed roadmap to stepwise integration of genetics in family medicine and clinical research.
  Houwink Elisa Jf et al. Clinical and translational medicine 2013 Feb 2(1) 5
• Barriers and facilitators to dissemination and adoption of precision medicine among Hispanics/Latinos.
  Canedo Juan R et al. BMC public health 2020 May 20(1) 603
• Systematic development of a training program for healthcare professionals to improve communication about breast cancer genetic counseling with low health literate patients.
  van der Giessen Jeanine A M et al. Familial cancer 2020 Apr
• Artificial Intelligence in Dentistry: Chances and Challenges.
  Schwendicke F et al. Journal of dental research 2020 Apr 22034520915714
• Genetics and ESKD Disparities in African Americans.
  Umeukeje Ebele M et al. American journal of kidney diseases : the official journal of the National Kidney Foundation 2019 74(6) 811-821
• An approach to integrating exome sequencing for fetal structural anomalies into clinical practice.
  Vora Neeta L et al. Genetics in medicine : official journal of the American College of Medical Genetics 2020 Jan
• Development and mixed-methods evaluation of an online animation for young people about genome sequencing.
  Lewis Celine et al. European journal of human genetics : EJHG 2020 Jan
• Values clarification and parental decision making about newborn genomic sequencing.
  Peinado Susana et al. Health psychology : official journal of the Division of Health Psychology, American Psychological Association 2019 Dec

more

Genetics, diagnosis, management and future directions of research of phaeochromocytoma and paraganglioma: a position statement and consensus of the Working Group on endocrine hypertension of the European society of hypertension. Lenders Jacques W M et al. Journal of hypertension 2020 May

Main|Search|PHGKB






Last Posted: May 20, 2020

---

• Genetics, diagnosis, management and future directions of research of phaeochromocytoma and paraganglioma: a position statement and consensus of the Working Group on endocrine hypertension of the European society of hypertension.
  Lenders Jacques W M et al. Journal of hypertension 2020 May
• Quality of life drives patients’ preferences for secondary findings from genomic sequencing
  C Mighton et al, Eur J Hum Genet May 18, 2020
• Shortened consent forms for genome-wide sequencing: Parent and provider perspectives.
  Hitchcock Emma C et al. Molecular genetics & genomic medicine 2020 May e1254
• Maternal copy-number variations in the DMD gene as secondary findings in noninvasive prenatal screening.
  Brison Nathalie et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 21(12) 2774-2780
• Ubuntu philosophy and the consensus regarding incidental findings in genomic research: a heuristic approach.
  Ewuoso Cornelius et al. Medicine, health care, and philosophy 2020 Apr
• Cost-Effectiveness of Panel Tests for Multiple Pharmacogenes Associated With Adverse Drug Reactions: An Evaluation Framework.
  Plumpton Catrin O et al. Clinical pharmacology and therapeutics 2019 105(6) 1429-1438
• Genetic screening of children with suspected inherited bleeding disorders.
  Andersson Nadine G et al. Haemophilia : the official journal of the World Federation of Hemophilia 2020 Feb
• Current controversies in prenatal diagnosis 2: The 59 genes ACMG recommends reporting as secondary findings when sequencing postnatally should be reported when detected on fetal (and parental) sequencing.
  Amor David J et al. Prenatal diagnosis 2020 Feb
• Disclosure of Genetic Risk Revealed in a Research Study.
  Castellanos Angela et al. The New England journal of medicine 2020 Feb (8) 763-765
• Why genomics researchers are sometimes morally required to hunt for secondary findings.
  Koplin Julian J et al. BMC medical ethics 2020 Jan 21(1) 11

more

How can Australia integrate routine genetic sequencing in oncology: a qualitative study through an implementation science lens R O'Shea et al, Genetics in Medicine, May 28, 2020

Main|Search|PHGKB






Last Posted: May 28, 2020

---

• How can Australia integrate routine genetic sequencing in oncology: a qualitative study through an implementation science lens
  R O'Shea et al, Genetics in Medicine, May 28, 2020
• 'There is a lot of good in knowing, but there is also a lot of downs': public views on ethical considerations in population genomic screening.
  Smit Amelia K et al. Journal of medical ethics 2020 May
• Challenges in pharmacotherapy for older adults: a framework for pharmacogenomics implementation.
  Roman Youssef M et al. Pharmacogenomics 2020 May
• Comparison of indications and results of prenatal invasive diagnostic tests before and after the implementation of the use of cell-free fetal DNA: a tertiary referral center experience.
  Okmen Firat et al. Journal of assisted reproduction and genetics 2020 May
• Integration of Mobile Health Into Sickle Cell Disease Care to Increase Hydroxyurea Utilization: Efficacy and Implementation Study.
  Hankins Jane S et al. JMIR research protocols 2020 Apr
• Polygenic risk scores: from research tools to clinical instruments.
  Lewis Cathryn M et al. Genome medicine 2020 May 12(1) 44
• Women's responses and understanding of polygenic breast cancer risk information.
  Yanes T et al. Familial cancer 2020 May
• A machine learning-based approach to directly compare the diagnostic accuracy of myocardial perfusion imaging by conventional and cadmium-zinc telluride SPECT.
  Cantoni Valeria et al. Journal of nuclear cardiology : official publication of the American Society of Nuclear Cardiology 2020 May
• Challenges and opportunities of cfDNA analysis implementation in clinical practice: Perspective of the International Society of Liquid Biopsy (ISLB).
  Rolfo Christian et al. Critical reviews in oncology/hematology 2020 May 151102978
• How Will Artificial Intelligence Affect Patient-Clinician Relationships?
  Nagy Matthew et al. AMA journal of ethics 2020 May 22(5) E395-400

more

Factors associated with referral and completion of genetic counseling in women with epithelial ovarian cancer. Alimena Stephanie et al. International journal of gynecological cancer : official journal of the International Gynecological Cancer Society 2020 May

Main|Search|PHGKB




Last Posted: May 28, 2020

---

• Factors associated with referral and completion of genetic counseling in women with epithelial ovarian cancer.
  Alimena Stephanie et al. International journal of gynecological cancer : official journal of the International Gynecological Cancer Society 2020 May
• Impacts of genesurance considerations on genetic counselors' practice and attitudes.
  Thoreson Emily et al. Journal of genetic counseling 2020 May
• Genetic characteristics and follow-up of patients with fatty acid β-oxidation disorders through expanded newborn screening in a Northern Chinese population.
  Wang Shuting et al. Journal of pediatric endocrinology & metabolism : JPEM 2020 May
• In-house genetic counseling increases the detection of abnormal karyotypes-a 26-year experience in prenatal diagnosis in a single tertiary referral hospital in Poland.
  Bijok Julia et al. Journal of assisted reproduction and genetics 2020 May
• Telegenetics: Remote Counseling During the COVID-19 Pandemic.
  Mahon Suzanne M et al. Clinical journal of oncology nursing 2020 Jun 24(3) 244-248
• Genetic Counseling in the Time of COVID-19
  K Bruder et al, CDC Blog, May 22, 2020
• Patient-Centered Prenatal Genetic Counseling,
  School of Medicine, Continuing Education
• Genetic Counseling and NGS Screening for Recessive LGMD2A Families.
  Strafella Claudia et al. High-throughput 2020 May 9(2)
• Apert syndrome: prenatal diagnosis challenge.
  Vieira Catarina et al. BMJ case reports 2019 Dec 12(12)
• Management of ovarian cancer risk in women with BRCA1/2 pathogenic variants.
  Walker Melissa et al. CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne 2019 191(32) E886-E893

more