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International Journal of Neonatal Screening|October 26, 2021
Scalable Newborn Screening Solutions: Bioinformatics and Next-Generation SequencingNicole Ruiz-Schultz, Bryce Asay, Andreas RohrwasserGenetics in Medicine : Official Journal of the American College of Medical Genetics|January 14, 2021
Methods and feasibility study for exome sequencing as a universal second-tier test in newborn screeningNicole Ruiz-Schultz, David Sant, Stevie Norcross, et al.Hypertension (Dallas, Tex. : 1979)|January 24, 2007
Genetic susceptibility to essential hypertension: insight from angiotensinogenJean-Marc Lalouel, Andreas RohrwasserAmerican Journal of Hypertension|February 28, 2002
Power and replication in case-control studiesJean-Marc Lalouel, Andreas RohrwasserGenetics in Medicine : Official Journal of the American College of Medical Genetics|November 20, 2020
Toward newborn screening of metachromatic leukodystrophy: results from analysis of over 27,000 newborn dried blood spotsXinying Hong, Jessica Daiker, Martin Sadilek, et al.Journal of Neuromuscular Diseases|July 6, 2026
Myotonic dystrophy family registry. The patient experienceSofia Olmos, Danny Kuei, Kleed Cumming, et al.Advances in Genetics|March 25, 2008
From genetics to mechanism of disease liabilityAndreas Rohrwasser, Paul Lott, Robert B Weiss, et al.Journal of the American Society of Nephrology : JASN|February 22, 2001
Angiotensinogen in essential hypertension: from genetics to nephrologyJean-Marc Lalouel, Andreas Rohrwasser, Daniel Terreros, et al.BMC Pediatrics|April 1, 2022
Pain points in parents' interactions with newborn screening systems: a qualitative studyMike Conway, Truc Thuy Vuong, Kim Hart, et al.Journal of Clinical Microbiology|August 31, 2018
Whole-Genome Sequencing and Bioinformatic Analysis of Isolates from Foodborne Illness Outbreaks of Campylobacter jejuni and Salmonella entericaKelly F Oakeson, Jennifer Marie Wagner, Andreas Rohrwasser, et al.Pageof 4