Minjie Luo

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 11

Top Topics

Autism Spectrum Disorder

Top Venues

JCO precision oncology

Genetics in medicine : official journal of the American College of Medical Genetics

Journal of the National Cancer Institute

This page only lists publications with an associated author ORCID identifier.

Publications

Minjie Luo, Derek Wong, Kristin Zelley, Jinhua Wu, Jeffery Schubert, Elizabeth H Denenberg, Elizabeth A Fanning, Jiani Chen, Daniel Gallo, Netta Golenberg, Maha Patel, Laura K Conlin, Kara N Maxwell, Gerald B Wertheim, Lea F Surrey, Yiming Zhong, Garrett M Brodeur, Suzanne P MacFarland, Marilyn M Li
Identification of TP53 germline variants in pediatric patients undergoing tumor testing: strategy and prevalence. Journal of the National Cancer Institute 116 (8) (2024)
Phassawan Rungsiprakarn, Anne L Ryan, Daniel D Wong, Minjie Luo, Ken Kazahaya, Alexandre Arkader, Loretta M S Lau, Pamela Ajuyah, Erin Rudzinski, Portia A Kreiger, Derek J Roebuck, Lea F Surrey, Tiffany Siang Ying Foo
Keratin-Positive Giant Cell Tumor of Bone and Soft Tissue With HMGA2::NCOR2 Fusion in Children Under 10 With Response to Imatinib Therapy: A Case Series. JCO precision oncology 8 (2024)
Phassawan Rungsiprakarn, Anne L Ryan, Daniel D Wong, Minjie Luo, Ken Kazahaya, Alexandre Arkader, Loretta M S Lau, Pamela Ajuyah, Erin Rudzinski, Portia A Kreiger, Derek J Roebuck, Lea F Surrey, Tiffany Siang Ying Foo
Keratin-Positive Giant Cell Tumor of Bone and Soft Tissue With HMGA2::NCOR2 Fusion in Children Under 10 With Response to Imatinib Therapy: A Case Series. JCO precision oncology 8 (2024)
Minjie Luo, Laura K Conlin, Ramakrishnan Rajagopalan
Maximizing the Detection of Copy Number Variants in the Highly Homologous Deafness-Infertility Syndrome Locus in Standard-of-care Testing. Clinical chemistry (2023)
Robert Chen, Maria Alejandra Diaz-Miranda, Erfan Aref-Eshghi, Tiffiney R Hartman, Christopher Griffith, Jennifer L Morrison, Patricia G Wheeler, Erin Torti, Gabriele Richard, Margaret Kenna, Elizabeth T Dechene, Nancy B Spinner, Renkui Bai, Laura K Conlin, Ian D Krantz, Sami S Amr, Minjie Luo
Characterization of a possible founder synonymous variant in TECTA in multiple individuals with autosomal recessive hearing loss. Human mutation (2022)
Laura K Conlin, Erfan Aref-Eshghi, Deborah A McEldrew, Minjie Luo, Ramakrishnan Rajagopalan
Long-read sequencing for molecular diagnostics in constitutional genetic disorders. Human mutation 43 (11) (2022)
Yoel Hirsch, Chayada Tangshewinsirikul, Kevin T A Booth, Hela Azaiez, Devorah Yefet, Adina Quint, Tzvi Weiden, Zippora Brownstein, Michal Macarov, Bella Davidov, John G Pappas, Rachel Rabin, Margaret A Kenna, Andrea M Oza, Katherine Lafferty, Sami S Amr, Heidi L Rehm, Diana L Kolbe, Kathy Frees, Carla Nishimura, Minjie Luo, Chantal Farra, Cynthia C Morton, Sholem Y Scher, Josef Ekstein, Karen B Avraham, Richard J H Smith, Jun Shen
A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing. European journal of human genetics : EJHG 29 (6) (2021)
Jun Shen, Andrea M Oza, Ignacio Del Castillo, Hatice Duzkale, Tatsuo Matsunaga, Arti Pandya, Hyunseok P Kang, Rebecca Mar-Heyming, Saurav Guha, Krista Moyer, Christine Lo, Margaret Kenna, John J Alexander, Yan Zhang, Yoel Hirsch, Minjie Luo, Ye Cao, Kwong-Wai Choy, Yen-Fu Cheng, Karen B Avraham, Xinhua Hu, Gema Garrido, Miguel Angel Moreno-Pelayo, John Greinwald, Kejian Zhang, Yukun Zeng, Zippora Brownstein, Lina Basel-Salmon, Bella Davidov, Moshe Frydman, Tzvi Weiden, Narasimhan Nagan, Alecia Willis, Sarah E Hemphill, Andrew R Grant, Rebecca K Siegert, Marina T DiStefano, Sami S Amr, Michael J Bamshad, Ahmad N Abou Tayoun, null null
Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel. Genetics in medicine : official journal of the American College of Medical Genetics 21 (11) (2019)
Jaclyn Rosenthal, Ammar S Naqvi, Minjie Luo, Gerald Wertheim, Michele Paessler, Andrei Thomas-Tikhonenko, Susan R Rheingold, Vinodh Pillai
Heterogeneity of surface CD19 and CD22 expression in B lymphoblastic leukemia. American journal of hematology 93 (11) (2018)
Minjie Luo, Jinbo Fan, Tara L Wenger, Margaret H Harr, Melissa Racobaldo, Surabhi Mulchandani, Holly Dubbs, Elaine H Zackai, Nancy B Spinner, Laura K Conlin
CMIP haploinsufficiency in two patients with autism spectrum disorder and co-occurring gastrointestinal issues. American journal of medical genetics. Part A 173 (8) (2017)
Elizabeth Joyce Bhoj, Zhenming Yu, Qiaoning Guan, Rebecca Ahrens-Nicklas, Kajia Cao, Minjie Luo, Tanya Tischler, Matthew A Deardorff, Elaine Zackai, Avni B Santani
Phenotypic predictors and final diagnoses in patients referred for RASopathy testing by targeted next-generation sequencing. Genetics in medicine : official journal of the American College of Medical Genetics 19 (6) (2016)