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All papers authored by Peter Benn

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2019 P. Benn

ORCID

, 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

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Chiara Palka, Paolo Guanciali-Franchi, Elisena Morizio, Melissa Alfonsi, Marco Papponetti, Giulia Sabbatinelli, Giandomenico Palka, Giuseppe Calabrese, Peter Benn

ORCID

Non-invasive prenatal screening: A 20-year experience in Italy

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2018 Peter Benn

ORCID

, Sharon E. Plon

ORCID

, Diana W. Bianchi

ORCID

Current Controversies in Prenatal Diagnosis 2: NIPT results suggesting maternal cancer should always be disclosed

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Trudy McKanna, Allison Ryan, Shifra Krinshpun, Stephanie Kareht, Karen Marchand, Caitlin Grabarits, Marwan Ali, Ashley McElheny, Kate Gardiner, Kay LeChien, Melissa Hsu, Daniel Saltzman, Melissa Stosic, Kimberly Martin, Peter Benn

ORCID

Fetal fraction-based risk algorithm for non-invasive prenatal testing: screening for trisomy 13, 18, and triploidy in women with low cell-free fetal DNA: Risk and fetal fraction

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P. Benn

ORCID

, F. R. Grati

Genome-wide non-invasive prenatal screening for all cytogenetically visible imbalances

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2017 K. Martin, S. Iyengar, A. Kalyan, C. Lan, A. L. Simon

ORCID

, M. Stosic, K. Kobara, H. Ravi, T. Truong, A. Ryan, Z. P. Demko, P. Benn

ORCID

Clinical experience with a single-nucleotide polymorphism-based non-invasive prenatal test for five clinically significant microdeletions: MARTIN et al

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Francesca Romana Grati

ORCID

, Peter Benn

ORCID

Comment on “The clinical utility of genome-wide non invasive prenatal screening”: Correspondence

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Peter Benn

ORCID

, 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

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

2016 Peter Benn

ORCID

The Significance of Test Failures in Noninvasive Prenatal Screening for Fetal Aneuploidy Using Cell-free DNA

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