U. Harper

发表

Gene expression profiling of human sarcomas: insights into sarcoma biology.

P. Meltzer, A. Glatfelter, C. Antonescu, 2005, Cancer research.

Loss-of-Function Fibroblast Growth Factor Receptor-2 Mutations in Melanoma

P. Meltzer, P. Pollock, J. Trent, 2009, Molecular Cancer Research.

A Hereditary Form of Small Intestinal Carcinoid Associated With a Germline Mutation in Inositol Polyphosphate Multikinase.

R. Agarwala, A. Schäffer, S. Szymczak, 2015, Gastroenterology.

LOSS-OF-FUNCTION FGFR2 MUTATIONS IN MELANOMA

P. Meltzer, J. Trent, S. Byron, 2017 .

LOSS-OF-FUNCTION FGFR 2 MUTATIONS IN MELANOMA

P. Meltzer, J. Trent, S. Byron, 2012 .

Multiplexed CRISPR/Cas9-mediated knockout of 19 Fanconi anemia pathway genes in zebrafish revealed their roles in growth, sexual development and fertility

R. Sood, S. Chandrasekharappa, D. Kimble, 2018, PLoS genetics.

The vitamin B12 processing enzyme, mmachc, is essential for zebrafish survival, growth and retinal morphology.

A. Elkahloun, V. Hoffmann, C. Venditti, 2020, Human molecular genetics.

High frequency of BRAF mutations in nevi

P. Meltzer, P. Pollock, J. Trent, 2003, Nature Genetics.

High-throughput gene targeting and phenotyping in zebrafish using CRISPR/Cas9

Kevin Bishop, Lisha Xu, Anupam Prakash, 2015, Genome research.

Genetic background modifies phenotypic severity and longevity in a mouse model of Niemann-Pick disease type C1

D. Watkins-Chow, W. Pavan, K. Broman, 2020, Disease Models & Mechanisms.

Highly Efficient Cpf1-Mediated Gene Targeting in Mice Following High Concentration Pronuclear Injection

D. Watkins-Chow, W. Pavan, S. Burgess, 2016, G3: Genes, Genomes, Genetics.

Highly-efficient Cpf1-mediated gene targeting in mice following high concentration pronuclear injection

D. Watkins-Chow, W. Pavan, S. Burgess, 2016, bioRxiv.

GWAS reveals new recessive loci associated with non-syndromic facial clefting.

B. Solomon, S. Chandrasekharappa, U. Harper, 2012, European journal of medical genetics.

Microarray expression profiling in melanoma reveals a BRAF mutation signature

Markus Ringnér, Pamela M Pollock, Peter Hersey, 2004, Oncogene.

Genetic heterogeneity in Finnish hereditary prostate cancer using ordered subset analysis

J. Schleutker, Tiina Wahlfors, T. Tammela, 2012, European Journal of Human Genetics.

Redundant mechanisms driven independently by RUNX1 and GATA2 for hematopoietic development

Paul Liu, S. Dell’Orso, R. Sood, 2021, bioRxiv.

Genome‐wide linkage scan for prostate cancer susceptibility in Finland: Evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21‐q22

Claire L. Simpson, J. Schleutker, Tiina Wahlfors, 2011, International journal of cancer.

Comparison of Wound Closure after Burn and Cold Injury in Human Skin Equivalents

P. Pollock, H. Ananthaswamy, U. Harper, 2006 .

CRISPR-Mediated Triple Knockout of SLAMF1, SLAMF5 and SLAMF6 Supports Positive Signaling Roles in NKT Cell Development

Silvia Preite, P. Schwartzberg, U. Harper, 2016, PloS one.

Pooling/bootstrap-based GWAS (pbGWAS) identifies new loci modifying the age of onset in PSEN1 p.Glu280Ala Alzheimer's disease

J. C. Correa, J. Swanson, N. Schork, 2012, Molecular Psychiatry.

Recombination mapping using Boolean logic and high-density SNP genotyping for exome sequence filtering.

D. Adams, C. Boerkoel, W. Gahl, 2012, Molecular genetics and metabolism.

Paternal or Maternal Uniparental Disomy of Chromosome 16 Resulting in Homozygosity of a Mutant Allele Causes Fanconi Anemia

E. Ostrander, J. Wagner, A. Auerbach, 2016, Human mutation.

Identification of FGFR2 as a novel melanoma oncogene

P. Meltzer, P. Pollock, S. Pavey, 2005 .