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Alexander Bisignano

Observed name: A. Bisignano
ORCID: 0000-0003-4120-6470
Observed ORCID: 0000-0003-4120-6470
OpenAlex ID: A5030096218
PGD and aneuploidy screening for 24 chromosomes: advantages and disadvantages of competing platforms
2011 · A. Bisignano, D. Wells, et al. · Reproductive BioMedicine Online · 35
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Past performance of assisted reproduction technologies as a model to predict future progress: a proposed addendum to Moore’s law
2012 · Jacques Cohen, Mina Alikani, et al. · Reproductive BioMedicine Online · 25
Validation of a Self-administrable, Saliva-based RT-qPCR Test Detecting SARS-CoV-2
2020 · Meghan Miller, Michael Jansen, et al. · medRxiv · 18
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Reply: PGD and aneuploidy screening for 24 chromosomes by genome-wide SNP analysis: a responsible path towards greater utility
2011 · Alexander Bisignano, Dagan Wells, et al. · Reproductive BioMedicine Online · 5
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Retracted: Validation of a multiplex genotyping platform using a novel genomic database approach
2015 · Charlotte Rivera-Garcia, Sara L. Bristow, et al. · Genetics in Medicine · 3
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Biomarkers for infertility and recurrent pregnancy loss
2014 · Sara L Bristow, Neha Kumar, et al. · Reproductive BioMedicine Online · 3
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Technical Performance of a 430-Gene Preventative Genomics Assay to Identify Multiple Variant Types Associated with Adult-Onset Monogenic Conditions, Susceptibility Loci, and Pharmacogenetic Insights
2022 · Ari Silver, Gabriel A. Lazarin, et al. · Journal of Personalized Medicine · 1
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HPTN 069/ACTG A5305: phase II study of maraviroc-containing regimens for HIV PrEP in US women; Postive impact of a randomized controlled trial of the Uthando Lwethu ("Our Love") intervention on rates of couples HIV testing in rural South Africa
2016 · Adam J. Ericsen, Michael Lauck, et al. · 1
Do you really know your ethnicity? Comparing self-reported and genetically-predicted ethnicity: clinical implications
2015 · R. Shraga, S.L. Bristow, et al. · Fertility and Sterility · 1
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eP376: NGS detection of NUDT15 6-bp insertion and UGT1A1 (TA) repeat polymorphism on a preventative genomics assay
2022 · Meghan Miller, Michael Jansen, et al. · Genetics in Medicine
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Technical Performance of a 455-Gene Preventative Genomics Assay to Identify Multiple Variant Types Associated with Adult-Onset Monogenic Conditions, Susceptibility Loci, and Pharmacogenetic Insights
2021 · Ari Silver, Gabriel Lazarin, et al. · Genetics in Medicine
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Clinical Utility of Expanded Pan Dyslipidemia and Statin-Induced Myopathy Genetic Testing
2020 · Malgorzata Jaremko, Meghan Miller, et al. · Journal of clinical lipidology
Identification of a Novel APOB Mutation in a Patient with Lifelong Hypercholesterolemia
2020 · Meghan Miller, Loba Alam, et al. · Journal of clinical lipidology
Pd25-10 Testing for Genetic Mutations in Severe Testicular Failure Using Commercialized Gene Sequencing Offers Novel Insight for Physicians and Patients
2020 · Matthew Pollard*, Saneal Rajanahally, et al. · The Journal of Urology
Comprehensive next generation sequencing assay and bioinformatic pipeline for identifying pathogenic variants associated with hereditary cancers.
2017 · Oscar Puig, Eugene Joseph, et al. · Journal of Clinical Oncology
Enrichment of genetic variants related to infertility in females seeking fertility treatment
2017 · Sasha E. Parets, Andrew Pollock, et al. · Fertility and Sterility
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Comprehensive Next Generation Sequencing Assay for Identifying Pathogenic Variants Associated With Cardiovascular Diseases
2017 · Eugene Joseph, Arun Manoharan, et al. · Journal of the American College of Cardiology
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Genetic influences on endocrine signaling in women
2015 · S.L. Bristow, R. Shraga, et al. · Fertility and Sterility
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Going beyond the guidelines: a call for expanded carrier screen based on an analysis of 3,208 clinical samples
2014 · N. Kumar, S. Rodriguez, et al. · Fertility and Sterility
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The role of classical and non-classical congenital adrenal hyperplasia (CAH) in infertilty: an analysis of 2000 clinical samples
2014 · S.L. Bristow, N. Kumar, et al. · Fertility and Sterility
To test or not to test? variable spectrum mutations (VSMS) in high impact diseases identified in 3,208 clinical samples screened via an expanded carrier screening platform
2014 · S. Rodriguez, N. Kumar, et al. · Fertility and Sterility
From carrier screening to single gene PGD: an analysis of 762 couples screened via an expanded carrier screening platform
2014 · N. Kumar, A. Bisignano, et al. · Fertility and Sterility
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An analysis of comprehensive carrier screening results for 1000 clinical samples: the importance of transparent disease classification & criteria for selection
2013 · A. Bisignano, N. Kumar, et al. · Fertility and Sterility
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Development and improvement of a new multi-genetic test for the detection of 221 of the most highly penetrant monogenic diseases
2012 · J.A. Horcajadas, J. Fischer, et al. · Fertility and Sterility
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A comparison of array technologies and next generation sequencing technologies in preconception genetic diagnosis
2012 · A. Bisignano, K. Ketterson, et al. · Fertility and Sterility
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Works count: 26
Citation count: 92
H-index: 4
I10-index: 3
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