Publications by authors named "Carrie Haverty"

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Utility of the US Preventive Services Task Force for Preeclampsia Risk Assessment and Aspirin Prophylaxis.
Thomas F McElrath, Arun Jeyabalan, Arkady Khodursky, Alison B Moe, Manfred Lee, Carrie Haverty

JAMA Netw Open· July 2025

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Molecular subtyping of hypertensive disorders of pregnancy.
Michal A Elovitz, Elaine P S Gee, Nathaniel Delaney-Busch, Alison B Moe, Mitsu Reddy, Carrie Haverty

Nat Commun· April 2025

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Impact of early preeclampsia prediction on medication adherence and behavior change: a survey of pregnant and recently-delivered individuals.
Alison Cowan, Carrie Haverty, Reece MacDonald, Arkady Khodursky

BMC Pregnancy Childbirth· March 2024

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Predictive RNA profiles for early and very early spontaneous preterm birth.
Joan Camunas-Soler, Elaine P S Gee, Mitsu Reddy, Jia Dai Mi, Mainou Thao, Carrie Haverty

Am J Obstet Gynecol· July 2022

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Results of the Genetic Counselor SARS-CoV-2 Impact Survey from the National Society of Genetic Counselors: Progress and penalty during the COVID-19 pandemic.
Vivian Pan, Megan Doerr, Christin Hoell, Lauren Ryan, Deanna J Erwin, Carrie Haverty

J Genet Couns· August 2021

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Noninvasive prenatal screening for patients with high body mass index: Evaluating the impact of a customized whole genome sequencing workflow on sensitivity and residual risk.
Dale Muzzey, James D Goldberg, Carrie Haverty

Prenat Diagn· February 2020

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Technology-Driven Noninvasive Prenatal Screening Results Disclosure and Management.
Aishwarya Arjunan, Rotem Ben-Shachar, Jamie Kostialik, Katherine Johansen Taber, Gabriel A Lazarin, Carrie Haverty

Telemed J E Health· January 2020

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Inaccuracies and shortcomings in "Adherence of cell-free DNA noninvasive prenatal screens to ACMG recommendations".
Katherine Johansen Taber, Carrie Haverty, Susan Hancock, James Goldberg

Genet Med· November 2019

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Correction: Inaccuracies and shortcomings in "Adherence of cell-free DNA noninvasive prenatal screens to ACMG recommendations".
Katherine Johansen Taber, Carrie Haverty, Susan Hancock, James Goldberg

Genet Med· November 2019

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Strategies to minimize false positives and interpret novel microdeletions based on maternal copy-number variants in 87,000 noninvasive prenatal screens.
Kristjan Eerik Kaseniit, Gregory J Hogan, Kevin M D'Auria, Carrie Haverty, Dale Muzzey

BMC Med Genomics· October 2018

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Response to "Noninvasive prenatal screening at low fetal fraction: comparing whole-genome sequencing and single-nucleotide polymorphism methods".
Dale Muzzey, Carrie Haverty, Eric A Evans, James D Goldberg

Prenat Diagn· July 2017

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Noninvasive prenatal screening at low fetal fraction: comparing whole-genome sequencing and single-nucleotide polymorphism methods.
Carlo G Artieri, Carrie Haverty, Eric A Evans, James D Goldberg, Imran S Haque

Prenat Diagn· May 2017

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Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 28-2004. Newborn twins with thrombocytopenia, coagulation defects, and hepatosplenomegaly.
Jeffrey M Lipton, Sjirk Westra, Carrie E Haverty, Drucilla Roberts, Nancy Lee Harris

N Engl J Med· September 2004

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47,XXX associated with malformations.
Carrie E Haverty, Angela E Lin, Ellen Simpson, M Anne Spence, Rick A Martin

Am J Med Genet A· February 2004

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