Publications by authors named "Sahoo Trilochan"

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Case Report: Unraveling complex genomic alterations in a case of chronic lymphocytic leukemia using optical genome mapping.
Leila Youssefian, Trilochan Sahoo, Jia-Chi Wang

Front Oncol· December 2025

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Correction: Case Report: Unraveling complex genomic alterations in a case of chronic lymphocytic leukemia using optical genome mapping.
Leila Youssefian, Sahoo Trilochan, Jia-Chi Wang

Front Oncol· December 2025

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Analytic Validation of Optical Genome Mapping in Hematological Malignancies.
Andy W C Pang, Karena Kosco, Nikhil S Sahajpal, Arthi Sridhar, Jen Hauenstein, Trilochan Sahoo

Biomedicines· December 2023

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The genomic basis of sporadic and recurrent pregnancy loss: a comprehensive in-depth analysis of 24,900 miscarriages.
Jenna Finley, Sara Hay, Jeannine Oldzej, Matthew M Meredith, Natasa Dzidic, Trilochan Sahoo

Reprod Biomed Online· July 2022

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Heterozygous intragenic deletions of FREM1 are not associated with trigonocephaly.
Angelika J Dawson, Karine Hovanes, Jing Liu, Sandra Marles, Cheryl Greenberg, Trilochan Sahoo

Clin Dysmorphol· April 2021

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Correction: Comprehensive analysis of 204 sporadic hydatidiform moles: revisiting risk factors and their correlations with the molar genotypes.
Yassemine Khawajkie, Nawel Mechtouf, Ngoc Minh Phuong Nguyen, Kurosh Rahimi, Magali Breguet, Trilochan Sahoo

Mod Pathol· June 2020

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Comprehensive analysis of 204 sporadic hydatidiform moles: revisiting risk factors and their correlations with the molar genotypes.
Yassemine Khawajkie, Nawel Mechtouf, Ngoc Minh Phuong Nguyen, Kurosh Rahimi, Magali Breguet, Trilochan Sahoo

Mod Pathol· May 2020

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Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed disease.
Andrew M Gross, Subramanian S Ajay, Vani Rajan, Carolyn Brown, Krista Bluske, Trilochan Sahoo

Genet Med· May 2019

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Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles.
Ngoc Minh Phuong Nguyen, Zhao-Jia Ge, Ramesh Reddy, Somayyeh Fahiminiya, Philippe Sauthier, Trilochan Sahoo

Am J Hum Genet· November 2018

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The genetics of recurrent hydatidiform moles: new insights and lessons from a comprehensive analysis of 113 patients.
Ngoc Minh Phuong Nguyen, Yassemine Khawajkie, Nawel Mechtouf, Maryam Rezaei, Magali Breguet, Trilochan Sahoo

Mod Pathol· July 2018

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ACOG and SMFM guidelines for prenatal diagnosis: Is karyotyping really sufficient?
Sara B Hay, Trilochan Sahoo, Mary K Travis, Karine Hovanes, Natasa Dzidic

Prenat Diagn· February 2018

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Comprehensive genetic analysis of pregnancy loss by chromosomal microarrays: outcomes, benefits, and challenges.
Trilochan Sahoo, Natasa Dzidic, Michelle N Strecker, Sara Commander, Mary K Travis

Genet Med· January 2017

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Expanding noninvasive prenatal testing to include microdeletions and segmental aneuploidy: cause for concern?
Trilochan Sahoo, Karine Hovanes, Michelle N Strecker, Natasa Dzidic, Sara Commander

Genet Med· March 2016

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Simulation of path delay multiplexing-based Fourier transform spectrometer for fiber Bragg grating interrogation.
Pandian Chelliah, Trilochan Sahoo, Sheela Singh, Annie Sujatha

Appl Opt· October 2015

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Simulation of optically encoded multiplexing for parallel multipoint sensing.
C Babu Rao, Pandian Chelliah, Trilochan Sahoo

Appl Opt· June 2015

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Regions of homozygosity identified by oligonucleotide SNP arrays: evaluating the incidence and clinical utility.
Jia-Chi Wang, Leslie Ross, Loretta W Mahon, Renius Owen, Morteza Hemmat, Trilochan Sahoo

Eur J Hum Genet· May 2015

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Constitutional chromothripsis involving chromosome 19 in a child with subtle dysmorphic features.
Jia-Chi Wang, Thomas Fisker, Trilochan Sahoo

Am J Med Genet A· April 2015

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Discordant noninvasive prenatal testing and cytogenetic results: a study of 109 consecutive cases.
Jia-Chi Wang, Trilochan Sahoo, Steven Schonberg, Kimberly A Kopita, Leslie Ross

Genet Med· March 2015

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Concurrent triplication and uniparental isodisomy: evidence for microhomology-mediated break-induced replication model for genomic rearrangements.
Trilochan Sahoo, Jia-Chi Wang, Mohamed M Elnaggar, Pedro Sanchez-Lara, Leslie P Ross

Eur J Hum Genet· January 2015

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Abnormalities in spontaneous abortions detected by G-banding and chromosomal microarray analysis (CMA) at a national reference laboratory.
Boris T Wang, Thomas P Chong, Fatih Z Boyar, Kimberly A Kopita, Leslie P Ross, Trilochan Sahoo

Mol Cytogenet· June 2014

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Mosaic isochromosome 15q and maternal uniparental isodisomy for chromosome 15 in a patient with morbid obesity and variant PWS-like phenotype.
Jia-Chi Wang, Mary Vaccarello-Cruz, Leslie Ross, Renius Owen, Victoria M Pratt, Trilochan Sahoo

Am J Med Genet A· July 2013

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Genotype-phenotype analysis of recombinant chromosome 4 syndrome: an array-CGH study and literature review.
Morteza Hemmat, Omid Hemmat, Arturo Anguiano, Fatih Z Boyar, Mohammed El Naggar, Trilochan Sahoo

Mol Cytogenet· May 2013

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Duplication of OCRL and adjacent genes associated with autism but not Lowe syndrome.
Richard J Schroer, Arthur L Beaudet, Marwan Shinawi, Trilochan Sahoo, Ankita Patel

Am J Med Genet A· October 2012

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Characterization of a complex rearrangement involving duplication and deletion of 9p in an infant with craniofacial dysmorphism and cardiac anomalies.
Daniel L Di Bartolo, Mohamed El Naggar, Renius Owen, Trilochan Sahoo, Fred Gilbert

Mol Cytogenet· July 2012

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BCR-JAK2 fusion as a result of a translocation (9;22)(p24;q11.2) in a patient with CML-like myeloproliferative disease.
Mohamed M Elnaggar, Sally Agersborg, Trilochan Sahoo, Ati Girgin, Wanlong Ma

Mol Cytogenet· May 2012

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