Dr. Hanlee P Ji M.D.
Hematologist-Oncologist | Hematology & Oncology
875 Blake Wilbur Drive Stanford Cancer Inst Stanford CA, 94305About
Dr. Hanlee Ji is a hematologist oncologist practicing in Stanford, CA. Dr. Ji specializes in the diagnosis, treatment and prevention of blood diseases such as anemia, hemophilia, sickle-cell disease, leukemia and lymphoma. Hematologist Oncologists are also trained in the study of cancer and its attack on other organs.
Board Certification
Internal MedicineAmerican Board of Internal MedicineABIM- Medical Oncology- 2004
Provider Details
Expert Publications
Data provided by the National Library of Medicine- A functional assay for mutations in tumor suppressor genes caused by mismatch repair deficiency.
- Molecular inversion probes reveal patterns of 9p21 deletion and copy number aberrations in childhood leukemia.
- Targeted deep resequencing of the human cancer genome using next-generation technologies.
- A flexible approach for highly multiplexed candidate gene targeted resequencing.
- Ultrasensitive detection of rare mutations using next-generation targeted resequencing.
- Efficient targeted resequencing of human germline and cancer genomes by oligonucleotide-selective sequencing.
- The Human OligoGenome Resource: a database of oligonucleotide capture probes for resequencing target regions across the human genome.
- Targeted sequencing library preparation by genomic DNA circularization.
- Performance comparison of whole-genome sequencing platforms.
- Improving bioinformatic pipelines for exome variant calling.
- Identification of a novel deletion mutant strain in that results in a microsatellite instability phenotype.
- Quantitative and Sensitive Detection of Cancer Genome Amplifications from Formalin Fixed Paraffin Embedded Tumors with Droplet Digital PCR.
- RVD: a command-line program for ultrasensitive rare single nucleotide variant detection using targeted next-generation DNA resequencing.
- Systematic genomic identification of colorectal cancer genes delineating advanced from early clinical stage and metastasis.
- High sensitivity detection and quantitation of DNA copy number and single nucleotide variants with single color droplet digital PCR.
Clinical Trials
Publications
- Alytical chemistryHigh sensitivity detection and quantitation of D copy number and single nucleotide variants with2014
- Jourl of data mining in genomics & proteomicsIdentification of Insertion Deletion Mutations from Deep Targeted Resequencing.2013
- ANLS OF APPLIED STATISTICSDETECTING MUTATIONS IN MIXED SAMPLE SEQUENCING DATA USING EMPIRICAL BAYES2012
- TURE BIOTECHNOLOGYPerformance comparison of whole-genome sequencing platforms2012
- Translatiol medicine (Sunnyvale, Calif.)Quantitative and Sensitive Detection of Cancer Genome Amplifications from Formalin Fixed Paraffin2012
- BMC BIOTECHNOLOGYTargeted sequencing library preparation by genomic D circularization2011
- TURE BIOTECHNOLOGYEfficient targeted resequencing of human germline2011
- PERSOLIZED MEDICINEGenetic-based biomarkers and next-generation sequencing2011
- CANCER RESEARCHOncogenic BRAF Mutation with CDKN2A Ictivation Is Characteristic of a Subset of Pediatric Malignt2010
- JOURL OF TRANSLATIOL MEDICINEIdentification of a biomarker panel using a multiplex proximity ligation2009
- TURE BIOTECHNOLOGYNext-generation D sequencing2008
- PROCEEDINGS OF THE TIOL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMMultigene amplification and massively parallel sequencing for cancer mutation discovery2007
- TURE METHODSMultiplexed protein detection by proximity ligation for cancer biomarker validation2007
- JOURL OF ALZHEIMERS DISEASEUnder-expression of Kalirin-7 increases iNOS activity in cultured cells2007
- TURE BIOTECHNOLOGYReproducibility Probability Score2006
- TURE BIOTECHNOLOGYThe MicroArray Quality Control2006
- TURE BIOTECHNOLOGYData quality in genomics and microarrays2006
- CANCER RESEARCHMolecular inversion probe alysis of gene copy alterations reveals distinct categories of colorectal2006
- HUMAN MOLECULAR GENETICSA functiol assay for mutations in tumor suppressor genes caused by mismatch repair deficiency2001
- AMERICAN JOURL OF MEDICAL GENETICSSpondyloepimetaphyseal dysplasia with joint laxity (SEMDJL)1999
- AMERICAN JOURL OF HUMAN GENETICSMolecular classification of the inherited hamartoma polyposis syndromes1998
- AMERICAN JOURL OF HUMAN GENETICSInherited mutations in PTEN that are associated with breast cancer, Cowden disease1997
- CELLHOTSPOTS FOR UNSELECTED TY1 TRANSPOSITION EVENTS ON YEAST CHROMOSOME-III ARE NEAR TRANSFER1993
- Nucleic acids researchA programmable method for massively parallel targeted sequencing.2014
- Analytical chemistryHigh sensitivity detection and quantitation of DNA copy number and single nucleotide variants2014
- BMC MEDICAL GENOMICSSystematic genomic identification of colorectal cancer genes delineating advanced from early2013
- BMC research notesRVD: a command-line program for ultrasensitive rare single nucleotide variant detection using2013
- Journal of data mining in genomics & proteomicsIdentification of Insertion Deletion Mutations from Deep Targeted Resequencing.2013
- ANNALS OF APPLIED STATISTICSDETECTING MUTATIONS IN MIXED SAMPLE SEQUENCING DATA USING EMPIRICAL BAYES2012
- GENOME MEDICINEImproving bioinformatic pipelines for exome variant calling2012
- NATURE BIOTECHNOLOGYPerformance comparison of whole-genome sequencing platforms2012
- NUCLEIC ACIDS RESEARCHA cross-sample statistical model for SNP detection in short-read sequencing data2012
- Translational medicine (Sunnyvale, Calif.)Quantitative and Sensitive Detection of Cancer Genome Amplifications from Formalin Fixed Paraffin2012
- BioDiscoveryIdentification of a novel deletion mutant strain in Saccharomyces cerevisiae that results in a0
- NUCLEIC ACIDS RESEARCHUltrasensitive detection of rare mutations using next-generation targeted resequencing2012
- Nucleic acids researchThe Human OligoGenome Resource2012
- BMC BIOTECHNOLOGYTargeted sequencing library preparation by genomic DNA circularization2011
- NATURE BIOTECHNOLOGYEfficient targeted resequencing of human germline2011
- PLOS ONEA Flexible Approach for Highly Multiplexed Candidate Gene Targeted Resequencing2011
- PERSONALIZED MEDICINEGenetic-based biomarkers and next-generation sequencing2011
- CANCER RESEARCHOncogenic BRAF Mutation with CDKN2A Inactivation Is Characteristic of a Subset of Pediatric2010
- BiometrikaDetecting simultaneous changepoints in multiple sequences.2010
- BIOTECHNOLOGY AND GENETIC ENGINEERING REVIEWS, VOL 27Targeted deep resequencing of the human cancer genome using next-generation technologies2010
- JOURNAL OF TRANSLATIONAL MEDICINEIdentification of a biomarker panel using a multiplex proximity ligation2009
- CANCER GENETICS AND CYTOGENETICSMolecular inversion probes reveal patterns of 9p21 deletion2009
- BIOINFORMATICSDisperse-a software system for design of selector probes for exon resequencing applications2009
- Methods in molecular biology (Clifton, N.J.)Molecular inversion probe assay for allelic quantitation.2009
- NATURE BIOTECHNOLOGYNext-generation DNA sequencing2008
- PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OMultigene amplification and massively parallel sequencing for cancer mutation discovery2007
- NUCLEIC ACIDS RESEARCHMultiplex amplification of all coding sequences within 10 cancer genes by Gene-Collector2007
- NATURE METHODSMultiplexed protein detection by proximity ligation for cancer biomarker validation2007
- JOURNAL OF ALZHEIMERS DISEASEUnder-expression of Kalirin-7 increases iNOS activity in cultured cells2007
- NATURE BIOTECHNOLOGYReproducibility Probability Score2006
- NATURE BIOTECHNOLOGYThe MicroArray Quality Control2006
- NATURE BIOTECHNOLOGYData quality in genomics and microarrays2006
- CANCER RESEARCHMolecular inversion probe analysis of gene copy alterations reveals distinct categories of2006
- HUMAN MOLECULAR GENETICSA functional assay for mutations in tumor suppressor genes caused by mismatch repair deficiency2001
- AMERICAN JOURNAL OF MEDICAL GENETICSSpondyloepimetaphyseal dysplasia with joint laxity (SEMDJL)1999
- AMERICAN JOURNAL OF HUMAN GENETICSMolecular classification of the inherited hamartoma polyposis syndromes1998
- AMERICAN JOURNAL OF HUMAN GENETICSInherited mutations in PTEN that are associated with breast cancer, Cowden disease1997
- CELLHOTSPOTS FOR UNSELECTED TY1 TRANSPOSITION EVENTS ON YEAST CHROMOSOME-III ARE NEAR TRANSFER1993
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