Portuguese Health System – Challenges in Times of Genomics by André Gonçalo Dias Pereira

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The impact of a mainstream genetic testing pathway and socioeconomic factors on the uptake of germline genetic testing in breast cancer patients: results of the nationwide GENE-SMA... by Chiem Leonardo de Jong, Sabine Siesling, Ghita Carola Wilhelmina Maria Puts, Agnes Jager, Margreet Geertruda Elia Maria Ausems

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Health care providers’ experiences with genetic testing in patients at risk for hereditary angioedema by Dawn A. Laney, MS, Tricia D. Lee, MD, Jared Druss, BS, Ruth L. O’Keefe, BA, Patti Engel, RN, Marc Riedl, MD, MS

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Genetics healthcare providers' experiences counseling patients with results from consumer genomic testing by Magan Trottier, Dina Green, Hannah Ovadia, Amanda Catchings, Julia Gruberg, Victoria Groner, Catherine Fanjoy, Sita Dandiker, Kathleen Blazer, Jada G. Hamilton, Kenneth Offit

Subjects: “…consumer‐initiated genetic testing…”
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Guidelines for genetic testing of healthy adults who deposit samples and related data in bioresource collections and biobanks by E. E. Baranova, Ksenia Dmitrievna Fedulova, A. S. Glotov, V. L. Izhevskaya

Subjects: “…genetic testing…”
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THE GENETIC SUSCEPTIBILITY TO ATHEROSCLEROSIS by T. V. Kozhanova, E. V. Neudakhin, S. S. Zhilina, T. I. Mescheryakova, A. A. Abramov, E. N. Lukash, A. G. Prityko

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Yield of Genetic Testing in Children with Autism Spectrum Disorder – A Single-Center Experience by Kriti Arora, Minakshi Balwani, Akash Wakchaure, Gouri R Passi

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BEYOND TRADITIONAL DENTISTRY: THE RISE OF GENOMIC AND PERSONALIZED ORAL HEALTH by Laurenţiu-Camil Bohîlţea, Claudia Florina Bogdan-Andreescu, Cristina-Crenguţa Albu, Alexandru Burcea, Cristian-Viorel Poalelungi, Andreea Mariana Bănățeanu, Tudor Petru Ionescu

Subjects: “…genetic testing; pharmacogenomics; precision dentistry…”
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Overview of ADPKD in Pregnancy by Ruth E. Campbell, Charles L. Edelstein, Michel Chonchol

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An infant with glutaric aciduria type IIc diagnosed with a novel mutation by Sedat Işıkay, Ayhan Yaman, Serdar Ceylaner

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An attractive alternative to prenatal diagnosis: a case report of preimplantation genetic testing in familial cardiomyopathy by Shubhra Pandey, MBBS, DGO, FRM, Parth Khandhedia, MBBS, DGO

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Oncology Specialists' Perceptions and Insights Into Dihydropyrimidine Dehydrogenase Testing in Palestine by Mohammad Dweib, Hussein Hallak, Hani Hour, Asmahan Alzeer, Raya Fatafta, Leen Albaw

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Biallelic Mismatch Repair Deficiency in Children and Adolescents: A Review of Published and Unpublished Data from India—Need for an Indian Consortium by Gazel Sainulabdin, Purva Kanvinde, Ritika Khurana, Sangeeta Mudaliar, Vasudeva Bhat K, Anju Shukla, V. P. Krishnan, Yamini Krishnan

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Perceptions on Genetic and Genome Screening among College Students in the Emirates of Abu Dhabi by Habiba Alsafar, Deema Islayem, Reem Almansoori, Tahnoon Alnahyan, Abdulla Alhammadi, Raven Haan, Guan Tay

Subjects: “…genetic testing…”
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The role of molecular genetic testing in modern breast health management by M.J. Kotze, J. Malan, R. Pienaar, J. Apffelstaedt

Subjects: “…molecular genetic testing…”
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Prevalence of Constitutional Pathogenic Variant in a Cohort of 348 Patients With Multiple Primary Cancer Addressed in Oncogenetic Consultation by Mathis Lepage, Nancy Uhrhammer, Ioana Molnar, Maud Privat, Flora Ponelle‐Chachuat, Mathilde Gay‐Bellile, Yannick Bidet, Mathias Cavaillé

Subjects: “…genetic testing…”
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Allele Frequencies and Genotypes for the Ryanodine Receptor 1 Variant Causing Malignant Hyperthermia and Fatal Rhabdomyolysis With Hyperthermia in Horses by Monica Aleman, Molly McCue, Rebecca R. Bellone

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ARRHYTHMOGENIC CARDIOMYOPATHY OF THE RIGHT VENTRICLE COMORBID WITH HEMODYNAMICALLY SIGNIFICANT SECONDARY INTERATRIAL SEPTAL DEFECT by A. N. Shapieva, E. V. Zaklyazminskaya, Yu. V. Frolova, M. A. Nechaenko, A. G. Shestak, S. L. Dzemeshkevich

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Detection of <i>M. tuberculosis</i> Using Cartridge-Based Technology in Patients with Negative Sputum Microscopy Results in a Regional Laboratory by P. I. Eliseev, E. I. Nikishova, A. Yu. Krupskaya, V. I. Shtraukh, E. S. Khimova, A. O. Maryandyshev

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COLQ-Mutant Congenital Myasthenic Syndromes by J Gordon Millichap

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