Publications by authors named "Priya Marathe"

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Unemployment in patients with histiocytic neoplasms is frequent and associated with clinical and treatment characteristics.
Anne S Reiner, Dana Bossert, Allison M Sigler, Jen Silvers, Kathleen Brewer, Priya H Marathe

Haematologica· December 2025

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Step-down management of fever and neutropenia in low-risk pediatric and adolescent-young adult oncology patients is safe and effective: a single center experience.
Priya H Marathe, Christine Camacho-Bydume, Charlie White, Audrey Mauguen, Michael Kinnaman

Pediatr Hematol Oncol· December 2025

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Patient and providers' perspectives on using the GUÍA digital tool to enhance genomic results disclosure.
Jacqueline A Odgis, Sabrina A Suckiel, Laura Golfinopoulos, Nicole R Kelly, Katherine E Bonini, Priya N Marathe

Genet Med Open· October 2025

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Implementing integrated genomic risk assessments for breast cancer: lessons learned from the Electronic Medical Records and Genomics study.
Cong Liu, Katherine D Crew, Jennifer Morse, Jodell E Linder, Antonis C Antoniou, Priya N Marathe

JAMIA Open· October 2025

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Symptoms, unmet needs, and quality of life in Erdheim-Chester disease: a longitudinal registry-based analysis.
Priya H Marathe, Anne S Reiner, Dana Bossert, Allison M Sigler, Deanna Fournier

Blood Adv· September 2025

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Implementing Integrated Genomic Risk Assessments for Breast Cancer: Lessons Learned from the eMERGE Study.
Cong Liu, Katherine Crew, Jennifer Morse, Jodell E Linder, Antonis C Antoniou, Priya N Marathe

medRxiv· May 2025

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Anxiety and depression in patients with histiocytic neoplasms and their associated clinical features.
Anne S Reiner, Yesne Alici, Denise D Correa, Dana Bossert, Allison M Sigler, Priya Marathe

Blood Adv· March 2025

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Investigating the Impact of Screen-Sharing Visual Aids during Genomic Results Disclosure via Telehealth in Diverse Families in the TeleKidSeq Pilot Study.
Jacqueline A Odgis, Nicole R Kelly, Monisha Sebastin, Laura Golfinopoulos, Beverly J Insel, Priya N Marathe

Public Health Genomics· February 2025

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Employing effective recruitment and retention strategies to engage a diverse pediatric population in genomics research.
Michelle A Ramos, Katherine E Bonini, Laura Scarimbolo, Nicole R Kelly, Beverly Insel, Priya N Marathe

Am J Hum Genet· December 2024

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Pleuroparenchymal fibroelastosis as a late complication of childhood cancer therapy: A case series.
Priya H Marathe, Valeria Santibanez, Paul A Meyers, Maria L Padilla, Danielle N Friedman

Pediatr Blood Cancer· July 2024

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Evaluating parental personal utility of pediatric genetic and genomic testing in a diverse, multilingual population.
Priya N Marathe, Sabrina A Suckiel, Katherine E Bonini, Nicole R Kelly, Laura Scarimbolo

HGG Adv· July 2024

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Physician services and costs after disclosure of diagnostic sequencing results in the NYCKidSeq program.
Asem Berkalieva, Nicole R Kelly, Ashley Fisher, Samuel F Hohmann, Monisha Sebastin, Priya Marathe

Genet Med· January 2024

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The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic results disclosure in diverse families.
Sabrina A Suckiel, Nicole R Kelly, Jacqueline A Odgis, Katie M Gallagher, Monisha Sebastin, Priya N Marathe

Am J Hum Genet· December 2023

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Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients.
Noura S Abul-Husn, Priya N Marathe, Nicole R Kelly, Katherine E Bonini, Monisha Sebastin

Genet Med· September 2023

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Identification of copy number variants with genome sequencing: Clinical experiences from the NYCKidSeq program.
Katherine E Bonini, Amanda Thomas-Wilson, Priya N Marathe, Monisha Sebastin, Jacqueline A Odgis

Clin Genet· August 2023

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The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic counseling in racially and ethnically diverse families.
Sabrina A Suckiel, Nicole R Kelly, Jacqueline A Odgis, Katie M Gallagher, Monisha Sebastin, Priya N Marathe

medRxiv· July 2023

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Detection of mosaic variants using genome sequencing in a large pediatric cohort.
Jacqueline A Odgis, Katie M Gallagher, Atteeq U Rehman, Priya N Marathe, Katherine E Bonini

Am J Med Genet A· March 2023

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The TeleKidSeq pilot study: incorporating telehealth into clinical care of children from diverse backgrounds undergoing whole genome sequencing.
Monisha Sebastin, Jacqueline A Odgis, Sabrina A Suckiel, Katherine E Bonini, Miranda Di Biase, Priya Marathe

Pilot Feasibility Stud· March 2023

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Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients.
Noura S Abul-Husn, Priya N Marathe, Nicole R Kelly, Katherine E Bonini, Monisha Sebastin

medRxiv· March 2023

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Biochemical measures of ovarian function in female survivors of retinoblastoma treated with intra-arterial melphalan: an initial report.
Priya H Marathe, Ira J Dunkel, Jasmine H Francis, Zoltan Antal, Y Pierre Gobin

Ophthalmic Genet· December 2022

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Ethics Consultation Requests After Implementation of an Electronic Health Record Order.
Priya H Marathe, Hao Zhang, Liz Blackler, Peter D Stetson, Louis P Voigt

JCO Oncol Pract· September 2022

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Patients as experts: characterizing the most relevant patient-reported outcomes after hematopoietic cell transplantation.
Justin C Solle, Alexis Steinberg, Priya Marathe, Tamryn F Gray, Amy Emmert

Bone Marrow Transplant· January 2020

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Research participation among Asian American women at risk for cervical cancer: exploratory pilot of barriers and enhancers.
Ellen Giarelli, Deborah Watkins Bruner, Ethan Nguyen, Sarah Basham, Priya Marathe

J Immigr Minor Health· December 2011

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