Minjie Luo - Concepedia

Author

Minjie Luo

Children's Hospital of Philadelphia ORCID

Also Known As

Luo, Minjie, M Luo, M. Luo, MINJIE LUO, Meiqi Luo, Michael Gollob, Min-Jie Luo, Minjie Luo, Min⁃jie LUO, Vacha Shah

164

Publications

2.5K

Citations

H-Index

101

Concepts

All Affiliations

Children's Hospital of Philadelphia University of Pennsylvania Harvard University Southern Medical University Broad Institute

About

Minjie Luo is an author at Children's Hospital of Philadelphia specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	16	1K
2	Arts	2	2	130
3	Health Sciences	2	2	227
4	Education	1	1	13
5	Management	1	1	55

Minjie Luo

Publications

Citations

H-Index

Page 1

	Year	Citations
CAR T-cell therapy is effective for CD19-dim B-lymphoblastic leukemia but is impacted by prior blinatumomab therapy Vinodh Pillai, Kavitha Muralidharan, Wenzhao Meng, Blood Advances Cell TherapyPrior Blinatumomab TherapyMixed-phenotype Acute LeukemiaImmunologyPathology	2019	196
ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants Xi Luo, Simone Feurstein, Shruthi Mohan, Blood Advances	2019	151
Experience with carrier screening and prenatal diagnosis for 16 Ashkenazi Jewish genetic diseases Stuart A. Scott, Lisa Edelmann, Liu Liu, Human Mutation Genetic TestingGenetic EpidemiologyDiagnosisDisease Gene IdentificationGenetic Medicine	2010	145
Maternal uniparental disomy of chromosome 20: a novel imprinting disorder of growth failure Surabhi Mulchandani, Elizabeth Bhoj, Minjie Luo, Genetics in Medicine Developmental AnomalyChromatinInfertilityDevelopmental BiologyFertility	2015	119
Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel Jun Shen, Andrea M. Oza, Ignacio del Castillo, Genetics in Medicine GeneticsP.val37ile VariantsGenetic EpidemiologyPathologyCochlear Development	2019	98
ClinGen expert clinical validity curation of 164 hearing loss gene–disease pairs Marina T. DiStefano, Sarah E. Hemphill, Andrea M. Oza, Genetics in Medicine Genetic EpidemiologyAudiologyPathologyHearing DisordersNeurotology	2019	91
Automated Clinical Exome Reanalysis Reveals Novel Diagnoses Samuel W. Baker, Jill R. Murrell, Addie I. Nesbitt, Journal of Molecular Diagnostics	2018	84
An Ashkenazi Jewish SMN1 haplotype specific to duplication alleles improves pan-ethnic carrier screening for spinal muscular atrophy Minjie Luo, Liu Liu, Inga Peter, Genetics in Medicine Duplication AllelesAllelic VariantPan-ethnic CarrierGenetic DisorderGenetics	2013	82
NTRK Fusions Identified in Pediatric Tumors: The Frequency, Fusion Partners, and Clinical Outcome Xiaonan Zhao, Chelsea Kotch, Elizabeth Fox, JCO Precision Oncology	2021	80
A genotyping system capable of simultaneously analyzing >1000 single nucleotide polymorphisms in a haploid genome Hui‐Yun Wang, Minjie Luo, Irina V. Tereshchenko, Genome Research	2005	73

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