arrow
Back
M

Monica H. Wojcik

Boston Children's Hospital

29H-index
173Paper Count
3.5KCitation Count
Published Papers 69
Publication Date
Long-read transcriptome analysis using IsoRanker for identifying pathogenic variants in Mendelian conditions
err2026-08-25
err0
PREAI
errYong-Han Hank Cheng; Adriana E. Sedeño-Cortés; Jane E. Ranchalis; Katherine M. Munson; Mitchell R. Vollger; Elsa Balton; Casie A. Genetti; Jenny L. Wilson; Monica H. Wojcik; Alan H. Beggs; Michael J. Bamshad; Chia-Lin Wei; Katrina M. Dipple; Runjun D. Kumar; Mark D. Fleming; Ian A. Glass; Elizabeth E. Blue; Gail Jarvik; Jessica X. Chong; Daniela M. Witten
errShare
errSave
Multimodal Sequencing and Reanalysis Approaches to End the Diagnostic Odyssey of Individuals with Suspected Rare Monogenic Diseases
errGenes
IF2.8
err2026-05-31
err0
errOAAI
errCatherine A. Brownstein; Jill A. Madden; Wanqing Shao; Casie A. Genetti; Jason Chin; Vincent D. Ustach; Monica H. Wojcik; Anna Madden; Nathaniel Edisis; Heng Li; Daniel A. Johnson; Kirsty McWalter; Jessica Noya; Klaus Schmitz-Abe; Shira Rockowitz; Pankaj B. Agrawal; Scott Newman; Joseph M. Devaney; Paul Kruszka; Alan H. Beggs
errShare
errSave
Population-Based Study of Drug-Resistant Epilepsy Before Age Two: Predominance of Developmental and Epileptic Encephalopathies
err2026-04-23
err0
errOAAI
errStella Lilles; Klari Heidmets; Kaisa Teele Oja; Karit Reinson; Laura Roht; Sander Pajusalu; Monica H. Wojcik; Katrin Õunap; Inga Talvik
errShare
errSave
Biallelic variants in CELSR1 cause brain malformations, neurodevelopmental disorders and epilepsy in humans
err2026-01-13
err0
errOAAI
errClaudia M. Bonardi; Rikke S. Møller; Nuria Ruiz-Reig; Guoliang Chai; Camilla G. Madsen; Allan Bayat; Trine B. Hammer; Christina D. Fenger; Elena Gardella; Pawel Gawlinski; Mateusz Dawidziuk; Wojciech Wiszniewski; Monika Bekiesinska-Figatowska; Sara Cabet; Massimiliano Rossi; Gaetan Lesca; Evan Gouy; Birgit Jepsen; Tomasz S. Mieszczanek; Rossana Sanchez Russo; Eileen E. Barr; Katrin Õunap; Pilvi Ilves; Monica H. Wojcik; Mohamed Aittaleb; Klaus Brusgaard; Fadel Tissir; Guido Rubboli
errShare
errSave
Nationwide Study of Pediatric Drug-Resistant Epilepsy in Estonia: Lower Incidence and Insights into Etiology
err2026-01-06
err0
errOAAI
errLilles, Stella; Heidmets, Klari; Oja, Kaisa Teele; Reinson, Karit; Roht, Laura; Pajusalu, Sander; Wojcik, Monica H.; Ounap, Katrin; Talvik, Inga
errShare
errSave
Quality improvement initiative to optimize use of rapid genomic sequencing in a level IV NICU
err2026-01-01
err0
errOAAI
errD'Gama, Alissa M.; Hu, Rachel S.; Del Rosario, Maya C.; Hills, Sonia; Park, Hannah J.; Mehra, Anna-Therese; Tannenbaum, Laura S.; Morton, Sarah U.; Agrawal, Pankaj B.; Wojcik, Monica H.
errShare
errSave
Equity-focused implementation to enhance access to rare disease genomic research and understand diverse perspectives
err2026-01-01
err0
errOAAI
errMartinez, Eva; Serrano, Jillian; Abouhala, Siwaar; Neale, Ashana; VanNoy, Grace; Rehm, Heidi L.; O'Leary, Melanie; O'Donnell-Luria, Anne; Wojcik, Monica H.
errShare
errSave
Managing the Uncertainty of Precision While Navigating Goals of Care: A Framework for Collaborative Interpretation of Complex Genomic Testing Results in Critically-Ill Neonates
err2025-12-26
err1
PREAI
errCortezzo, Donnamaria E.; Callahan, Katharine Press; Chaudhari, Bimal P.; Weiss, Elliott M.; Wojcik, Monica Hsiung; Acharya, Krishna; Schlegel, Amy B.; Sullivan, Kevin M.; Fry, Jessica T.
errShare
errSave
Genetics and Stillbirth
err2025-11-26
err0
PREAI
errTsegaselassie Workalemahu; Monica H. Wojcik
errShare
errSave
Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function
err2025-10-22
err0
errOAAI
errReza Asadollahi; Aisha Ahmad; Paranchai Boonsawat; Jasmine Shahanoor Hinzen; Mareike Lohse; Boris Bouazza-Arostegui; Siqi Sun; Tillmann Utesch; Jonas D. Sommer; Dragana Ilic; Murugesh Padmanarayana; Kati Fischermanns; Mrinalini Ranjan; Moritz Boll; Chandran Ka; Amélie Piton; Francesca Mattioli; Bertrand Isidor; Katrin Õunap; Karit Reinson; Monica H. Wojcik; Christian R. Marshall; Saadet Mercimek-Andrews; Naomichi Matsumoto; Noriko Miyake; Bruno de Oliveira Stephan; Rachel Sayuri Honjo; Debora R. Bertola; Chong Ae Kim; Roman Yusupov; Heather C. Mefford; John Christodoulou; Joy Lee; Oliver Heath; Natasha J. Brown; Naomi Baker; Zornitza Stark; Martin Delatycki; Nicole J. Lake; Shimriet Zeidler; Linda Zuurbier; Saskia M. Maas; Chris C. de Kruiff; Farrah Rajabi; Lance H. Rodan; Stephanie A. Coury; Konrad Platzer; Henry Oppermann; Rami Abou Jamra; Skadi Beblo; Caroline Maxton; Robert Śmigiel; Hunter Underhill; Holly Dubbs; Alyssa Rosen; Katherine L. Helbig; Ingo Helbig; Sarah McKeown Ruggiero; Mark P. Fitzgerald; Dennis Kraemer; Carlos E. Prada; Jeffrey Tenney; Parul Jayakar; Sylvia Redon; Jérémie Lefranc; Kevin Uguen; Simone Race; Stephanie Efthymiou; Reza Maroofian; Henry Houlden; Sandra Coppens; Nicolas Deconinck; Balasubramaniem Ashokkumar; Perumal Varalakshmi; Vykunta Raju Gowda K; Fatemeh Eghbal; Ehsan Ghayoor Karimiani; Morteza Heidari; John Neidhardt; Marta Owczarek-Lipska; G. Christoph Korenke; Michael J. Bamshad; Philippe M. Campeau; Anna Lehman; Laura G. Hendon; Ingrid M. Wentzensen; Kristin G. Monaghan; Yanmin Chen; Anna Szuto; Ronald D. Cohn; Ping Yee Billie Au; Christoph Hübner; Felix Boschann; Kandamurugu Manickam; Daniel C. Koboldt; Aboulfazl Rad; Gabriela Oprea; Kristine K. Bachman; Andrea H. Seeley; Emanuele Agolini; Alessandra Terracciano; Piscopo Carmelo; Caleb Bupp; Bethany Grysko; Annick Rein-Rothschild; Bruria Ben Zeev; Amy Margolin; Jennifer Morrison; Aditi Dagli; Elliot Stolerman; Raymond J. Louie; Camerun Washington; Servi J. C. Stevens; Malou Heijligers; Fowzan S. Alkuraya; Jasmin Lisfeld; Axel Neu; Fabíola Paoli Monteiro; André Luiz Santos Pessoa; Antonio Edvan Camelo-Filho; Fernando Kok; Dwight Koeberl; Kacie Riley; Lydie Burglen; Diane Doummar; Bénédicte Héron; Cyril Mignot; Boris Keren; Perrine Charles; Caroline Nava; Felix P. Bernhard; Andrea A. Kühn; Sven Thoms; Ryan D. Morrie; Shila Mekhoubad; Eric M. Green; Sami J. Barmada; Aaron D. Gitler; Olaf Jahn; Jeong Seop Rhee; Christian Rosenmund; Mišo Mitkovski; Heinrich Sticht; Han Sun; Gerald Le Gac; Holger Taschenberger; Nils Brose; Jeremy S. Dittman; Anita Rauch; Noa Lipstein
errShare
errSave
Toward Same-Day Genome Sequencing in the Critical Care Setting
err2025-10-01
err1
PREAI
errWojcik, Monica H.; Larkin, Katie; Cipicchio, Michelle; Doupnik, Austin; Zhao, Chen; Cech, Cynthia; Lopez, Douglas; Chandrasekar, Jagadeeswaran; Leadbetter, Joanne; Mannion, John; Berg, Kendall; Golkaram, Mahdi; Osentowski, Mckenna; Freer, Megan; Lehmann, Taylor; Lee, Won-Mean; Ormbrek, Emily; Prindle, Marc J.; Nabavi, Melud; Chaturvedi, Amal; Seberino, Chuck; Baker, Daniel N.; Williams, Cara; Toledo, Diana; Malolepsza, Edyta; Fleharty, Mark; Oza, Andrea; Low, Sophie; Beggs, Alan H.; Genetti, Casie A.; Strickland, Gwendolyn; Anderson, Katherine N.; Chung, Wendy K.; Rehm, Heidi L.; Hofherr, Sean; Kokoris, Mark; Lennon, Niall
errShare
errSave
Implementing customized genomic sequencing reports to empower providers in safety-net Neonatal Intensive Care Units
err2025-08-13
err0
PREAI
errAlissa M. D’Gama; Jessica Douglas; Sonia Hills; Monica H. Wojcik; Casie A. Genetti; Aubrie Soucy Verran; Margaret G. Parker; Timothy W. Yu; Pankaj B. Agrawal
errShare
errSave
An end to genetic exceptionalism: reframing the ethics of genomic sequencing for rapid neonatal diagnosis
err2025-06-14
err0
PREAI
errKaiulani S Shulman; Kristen Fishler Malone; Hadley Stevens Smith; Bimal P. Chaudhari; Monica H Wojcik
errShare
errSave
Long-read sequencing is required for precision diagnosis of incontinentia pigmenti
err2025-06-12
err0
errOAAI
errMonica H. Wojcik; Robin D. Clark; Abdallah F. Elias; Casie A. Genetti; Jill A. Madden; Dana Simpson; Linda Golkar; Miranda P.G. Zalusky; Angela L. Miller; Araceli Rodriguez; Joy Goffena; Camille A. Dash; Nikhita Damaraju; Sophia B. Gibson; Sophie H.R. Storz; Zachary B. Anderson; Jonas A. Gustafson; Isabelle Thiffault; Emily G. Farrow; Tomi Pastinen; Danny E. Miller
errShare
errSave
Uncovering somatic mosaic variants of PIK3CA-related overgrowth disorders - three cases with different clinical presentations
err2025-01-13
err0
errOAAI
errTooming, M.; Mertsina, P.; Kahre, T.; Teek, R.; Vainumae, I.; Lilles, S.; Wojcik, M. H.; Ilves, P.; Ounap, K.
errShare
errSave
Genetic Test Utilization and Cost among Families of Children Evaluated for Genetic Conditions: An Analysis of USA Commercial Claims Data
err2025-01-08
err0
PREAI
errSmith, Hadley Stevens; Lakoma, Matthew; Hickingbotham, Madison R.; Cardeiro, Dawn; Callahan, Katharine P.; Wojcik, Monica H.; Wu, Ann Chen; Lu, Christine Y.
errShare
errSave
Estimating the sensitivity of genomic newborn screening for treatable inherited metabolic disorders
err2025-01-01
err2
PREAI
errBick, Sarah L.; Nathan, Aparna; Park, Hannah; Green, Robert C.; Wojcik, Monica H.; Gold, Nina B.
errShare
errSave
Multidimensional and Longitudinal Impact of a Genetic Diagnosis for Critically Ill Infants
err2024-11-08
err0
errOAAI
errWojcik, Monica H.; del Rosario, Maya C.; Feldman, Henry A.; Smith, Hadley Stevens; Holm, Ingrid A.
errShare
errSave