Peter Benn (P Benn)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 27

Top Venues

Circulation. Genomic and precision medicine

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology

Molecular genetics & genomic medicine

University of Connecticut Health Center

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Connecticut Health Center Aug 01 1990

United States

Professor Emeritus :: Genetics and Genome Science

Publications

Peter Benn, Jingwen Zhang, Daniel Lyons, Wenbo Xu, Samantha Leonard, Zachary P Demko
Accuracy of fetal fraction measurements in a single-nucleotide polymorphism-based noninvasive prenatal test. Prenatal diagnosis (2024)
Vivienne L Souter, Emily Becraft, Samantha Brummitt, Bryan J Gall, Brittany Prigmore, Yang Wang, Peter Benn
Reproductive Carrier Screening: Identifying Families at Risk for Familial Hypercholesterolemia in the United States. Circulation. Genomic and precision medicine 17 (2) (2024)
Vivienne L Souter, Emily Becraft, Samantha Brummitt, Bryan J Gall, Brittany Prigmore, Yang Wang, Peter Benn
Reproductive Carrier Screening: Identifying Families at Risk for Familial Hypercholesterolemia in the United States. Circulation. Genomic and precision medicine 17 (2) (2024)
Vivienne L Souter, Emily Becraft, Samantha Brummitt, Bryan J Gall, Brittany Prigmore, Yang Wang, Peter Benn
Reproductive Carrier Screening: Identifying Families at Risk for Familial Hypercholesterolemia in the United States. Circulation. Genomic and precision medicine 17 (2) (2024)
Vivienne L Souter, Emily Becraft, Samantha Brummit, Bryan J Gall, Brittany Prigmore, Yang Wang, Peter Benn
Reproductive Carrier Screening: Identifying Families at Risk for Familial Hypercholesterolemia in the United States. Circulation. Genomic and precision medicine (2024)
Vivienne L Souter, Emily Becraft, Samantha Brummitt, Bryan J Gall, Brittany Prigmore, Yang Wang, Peter Benn
Reproductive Carrier Screening: Identifying Families at Risk for Familial Hypercholesterolemia in the United States. Circulation. Genomic and precision medicine 17 (2) (2024)
John Williams, Peter Benn
Single gene non-invasive prenatal testing when the father is not available for testing; concerns regarding Wynn et al., Prenatal Diagnosis 2023. 43:1344-54. Prenatal diagnosis (2023)
Francesca Romana Grati, Ilaria Bestetti, Daria De Siero, Francesca Malvestiti, Nicoletta Villa, Elena Sala, Francesca Crosti, Valentina Parisi, Anna Maria Nardone, Gianluca Di Giacomo, Antonella Pettinari, Giada Tortora, Annamaria Montaldi, Annapaola Calò, Donatella Saccilotto, Sara Zanchetti, Paola Celli, Silvana Guerneri, Rosamaria Silipigni, Laura Cardarelli, Elisabetta Lippi, Simona Cavani, Michela Malacarne, Rita Genesio, Nicola Beltrami, Maria Carla Pittalis, Laura Desiderio, Mattia Gentile, Romina Ficarella, Maria Paola Recalcati, Ilaria Catusi, Maria Garzo, Lorena Miele, Cecilia Corti, Sara Ghezzo, Veronica Bertini, Francesca Cambi, Angelo Valetto, Barbara Facchinetti, Laura Bernardini, Anna Capalbo, Federica Balducci, Elisabetta Pelo, Barbara Minuti, Chiara Pescucci, Costanza Giuliani, Alessandra Renieri, Ilaria Longo, Rossella Tita, Giuseppe Castello, Rosario Casalone, Rossana Righi, Barbara Raso, Alessandro Civolani, Maria Cristina Muzi, Manuela di Natale, Luigia Varriale, Daniela Gasperini, Maria Cristina Nuzzi, Angelo Cellamare, Paola Casieri, Rosa Busuito, Caterina Ceccarini, Carla Cesarano, Orsola Privitera, Daniela Melani, Cristina Menozzi, Cristina Falcinelli, Olga Calabrese, Paola Battaglia, Antonella Tanzariello, Tamara Stampalija, Carmela Ardisia, Paolo Gasparini, Peter Benn, Antonio Novelli
Positive predictive values and outcomes for uninformative cell-free DNA tests: An Italian multicentric Cytogenetic and cytogenomic Audit of diagnOstic testing (ICARO study). Prenatal diagnosis (2022)
Howard S Cuckle, Peter Benn, Yuval Yaron
A founding father of reproductive genetics: Eugene Pergament (1933-2022). Prenatal diagnosis 42 (8) (2022)
Peter Benn
Rare autosomal trisomies detected by non-invasive prenatal testing. European journal of human genetics : EJHG 30 (12) (2022)
Valerie Kantor, Russ Jelsema, Wenbo Xu, Wendy DiNonno, Kathryn Young, Zachary P Demko, Peter Benn
Non-invasive prenatal screening for fetal triploidy using single nucleotide polymorphism-based testing: Differential diagnosis and clinical management in cases showing an extra haplotype. Prenatal diagnosis 42 (8) (2022)
Peter Benn, Andrei Rebarber
Non-invasive prenatal testing in the management of twin pregnancies. Prenatal diagnosis 41 (10) (2021)
Peter Benn, Howard S Cuckle, Eugene Pergament
The origins of aneuploidy research consortium. Prenatal diagnosis 41 (5) (2021)
P Mohan, J Lemoine, C Trotter, I Rakova, P Billings, S Peacock, C-Y Kao, Y Wang, F Xia, C M Eng, Peter Benn
Clinical experience with non-invasive prenatal screening for single-gene disorders (NIPT-SGD). Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology (2021)
Francesca Romana Grati, Francesca Malvestiti, Gloria Gallazzi, Silvia Saragozza, Beatrice Grimi, Cristina Agrati, Lara Branca, Federica Palumbo, Anna Trotta, Sara Chinetti, Giuseppe Simoni, Jose Ferreira, Peter Benn
Performance of conventional cytogenetic analysis on chorionic villi when only one cell layer, cytotrophoblast or mesenchyme alone, is analyzed. Prenatal diagnosis 41 (6) (2021)
Peter Benn
Uniparental disomy: Origin, frequency, and clinical significance. Prenatal diagnosis 41 (5) (2021)
Peter Benn
Obituary: Lillian YF Hsu, MD, FFACMG. Prenatal diagnosis 40 (11) (2020)
Howard S Cuckle, Peter Benn
Review of epidemiological factors (other than maternal age) that determine the prevalence of common autosomal trisomies. Prenatal diagnosis 41 (5) (2020)
Peter Benn, Francesca Romana Grati
Aneuploidy in first trimester chorionic villi and spontaneous abortions: Windows into the origin and fate of aneuploidy through embryonic and fetal development. Prenatal diagnosis 41 (5) (2020)
Peter Benn, F Malvestiti, B Grimi, F Maggi, G Simoni, F R Grati
Rare autosomal trisomies: comparison of detection through cell-free DNA analysis and direct chromosome preparation of chorionic villus samples. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 54 (4) (2019)
Herman L Hedriana, Kimberly A Martin, Daniel Saltzman, Paul Billings, Zachary P Demko, Peter Benn
Cell-free DNA fetal fraction in twin gestations in single-nucleotide polymorphism-based noninvasive prenatal screening. Prenatal diagnosis 40 (2) (2019)
T McKanna, A Ryan, S Krinshpun, S Kareht, K Marchand, C Grabarits, M Ali, A McElheny, K Gardiner, K LeChien, M Hsu, D Saltzman, M Stosic, K Martin, Peter Benn
Fetal fraction-based risk algorithm for non-invasive prenatal testing: screening for trisomies 13 and 18 and triploidy in women with low cell-free fetal DNA. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 53 (1) (2018)
Peter Benn, F R Grati
Genome-wide non-invasive prenatal screening for all cytogenetically visible imbalances. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 51 (4) (2018)
Peter Benn, Sharon E Plon, Diana W Bianchi
Current Controversies in Prenatal Diagnosis 2: NIPT results suggesting maternal cancer should always be disclosed. Prenatal diagnosis 39 (5) (2018)
Francesca Romana Grati, Peter Benn
Comment on "The clinical utility of genome-wide non invasive prenatal screening". Prenatal diagnosis 37 (10) (2017)
Peter Benn, Sushma Iyengar, Terrence Blaine Crowley, Elaine H Zackai, Evanette K Burrows, Solomon Moshkevich, Donna M McDonald-McGinn, Kathleen E Sullivan, Zachary Demko
Pediatric healthcare costs for patients with 22q11.2 deletion syndrome. Molecular genetics & genomic medicine 5 (6) (2017)
K Martin, S Iyengar, A Kalyan, C Lan, A L Simon, M Stosic, K Kobara, H Ravi, T Truong, A Ryan, Z P Demko, Peter Benn
Clinical experience with a single-nucleotide polymorphism-based non-invasive prenatal test for five clinically significant microdeletions. Clinical genetics 93 (2) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Peter Benn (P Benn)