Citation Impact
Citing Papers
Genome-Scale CRISPR-Cas9 Knockout Screening in Human Cells
2013 StandoutScience
Recurrent Fusion of TMPRSS2 and ETS Transcription Factor Genes in Prostate Cancer
2005 StandoutScience
Morphology of sporadic colorectal cancer with DNA replication errors
1998
The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives
1999 StandoutNature
AML1, the Target of Multiple Chromosomal Translocations in Human Leukemia, Is Essential for Normal Fetal Liver Hematopoiesis
1996 Standout
Essential role of mouse telomerase in highly proliferative organs
1998 StandoutNatureNobel
Treatment of Medulloblastoma with Hedgehog Pathway Inhibitor GDC-0449
2009 Standout
Positional cloning moves from perditional to traditional
1995
Pheochromocytomas, Multiple Endocrine Neoplasia Type 2, and von Hippel-Lindau Disease
1993
Sh2 And Sh3 Domains In Signal Transduction
1994
Oncogenic kinase signalling
2001 StandoutNature
The pressure rises: update on the genetics of phaeochromocytoma
2002
Functional receptor for GDNF encoded by the c-ret proto-oncogene
1996 Nature
Notch Receptors, Partners and Regulators: From Conserved Domains to Powerful Functions
1998
Molecular basis of the VHL hereditary cancer syndrome
2002 StandoutNobel
Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons
1994 Standout
Defects in enteric innervation and kidney development in mice lacking GDNF
1996 StandoutNature
SWI/SNF nucleosome remodellers and cancer
2011 Standout
Cancer Epigenetics: From Mechanism to Therapy
2012 Standout
AID Is Required for c-myc/IgH Chromosome Translocations In Vivo
2004 StandoutNobel
Telomere Shortening and Tumor Formation by Mouse Cells Lacking Telomerase RNA
1997 StandoutNobel
The Hallmarks of Cancer
2000 Standout
Lessons from Hereditary Colorectal Cancer
1996 Standout
Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia
2002 StandoutNobel
Synthetic peptides define critical contacts between elongin C, elongin B, and the von Hippel-Lindau protein
1999 StandoutNobel
Advances in the treatment of neurofibromatosis-associated tumours
2013
Regulation of angiogenesis by hypoxia: role of the HIF system
2003 StandoutNobel
A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10
1993
Tumor Microsatellite Instability and Clinical Outcome in Young Patients with Colorectal Cancer
2000
β-Arrestin1 Interacts with the Catalytic Domain of the Tyrosine Kinase c-SRC
2000 StandoutNobel
Large-Scale Variation Among Human and Great Ape Genomes Determined by Array Comparative Genomic Hybridization
2003
Initial sequence of the chimpanzee genome and comparison with the human genome
2005 StandoutNature
Chromosomal translocations in human cancer
1994 Nature
C-cell hyperplasia, pheochromocytoma and sympathoadrenal malformation in a mouse model of multiple endocrine neoplasia type 2B
2000
Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
2005 Standout
Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma
1996
A Cell Cycle Regulator Potentially Involved in Genesis of Many Tumor Types
1994 StandoutScience
Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret
1994 StandoutNature
Hereditary Colorectal Cancer
2003 Standout
The gene for the naevoid basal cell carcinoma syndrome acts as a tumour-suppressor gene in medulloblastoma
1997
The causes and consequences of genetic heterogeneity in cancer evolution
2013 StandoutNature
Loss of telomeric sites in the chromosomes ofMus musculus domesticus (Rodentia: Muridae) during Robertsonian rearrangements
1995
GDNF signalling through the Ret receptor tyrosine kinase
1996 StandoutNature
Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHL
1997
Enhanced Phosphatidylinositol 3-Kinase Activity and High Phosphorylation State of Its Downstream Signalling Molecules Mediated by Ret with the MEN 2B Mutation
1999
Hox11 paralogous genes are essential for metanephric kidney induction
2002 StandoutNobel
Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease
1994 Nature
Targeted and natural (piebald-lethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice
1994 Standout
Mutations of the RET proto-oncogene in Hirschsprung's disease
1994 Nature
Environmental and Heritable Factors in the Causation of Cancer — Analyses of Cohorts of Twins from Sweden, Denmark, and Finland
2000 Standout
Sporadic Pheochromocytomas Are Rarely Associated with Germline Mutations in thevhlTumor Suppressor Gene or theretProtooncogene1
1997
Renal agenesis and the absence of enteric neurons in mice lacking GDNF
1996 StandoutNature
Ubiquitination of hypoxia-inducible factor requires direct binding to the β-domain of the von Hippel–Lindau protein
2000 StandoutNobel
Genetic and epigenetic control in neural crest development
1994
p300/CBP and cancer
2004
Activating Mutations in the Epidermal Growth Factor Receptor Underlying Responsiveness of Non–Small-Cell Lung Cancer to Gefitinib
2004 Standout
Mucins and mucin binding proteins in colorectal cancer
2003
Colorectal Carcinoma: Diagnostic, Prognostic, and Molecular Features
2003
Genomic Sequence and Transcriptional Profile of the Boundary Between Pericentromeric Satellites and Genes on Human Chromosome Arm 10p
2003
Immunohistochemistry Versus Microsatellite Instability Testing in Phenotyping Colorectal Tumors
2002
Activation of RET as a Dominant Transforming Gene by Germline Mutations of MEN2A and MEN2B
1995 Science
Antioncogenes and human cancer.
1993
Inactivation of the PBRM1 tumor suppressor gene amplifies the HIF-response in VHL −/− clear cell renal carcinoma
2017 StandoutNobel
Cancer Cell Cycles
1996 StandoutScience
Expression of the c-ret proto-oncogene during mouse embryogenesis
1993
Histopathological Identification of Colon Cancer with Microsatellite Instability
2001
All in the (cancer) family
1993
PKD2 , a Gene for Polycystic Kidney Disease That Encodes an Integral Membrane Protein
1996 StandoutScience
After chronic myelogenous leukemia: tyrosine kinase inhibitors in other hematologic malignancies
2004
Gain-of-Function Mutations of c- kit in Human Gastrointestinal Stromal Tumors
1998 StandoutScience
W/kit gene required for interstitial cells of Cajal and for intestinal pacemaker activity
1995 StandoutNature
MUTATION OF THE VON HIPPEL-LINDAU TUMOUR SUPPRESSOR GENE IN CAPILLARY HAEMANGIOBLASTOMAS OF THE CENTRAL NERVOUS SYSTEM
1996
Classification of Intrinsically Disordered Regions and Proteins
2014 Standout
Tumor Microsatellite-Instability Status as a Predictor of Benefit from Fluorouracil-Based Adjuvant Chemotherapy for Colon Cancer
2003 Standout
CHASING THE CANCER DEMON
2000
Constitutive activation of c-kit in FMA3 murine mastocytoma cells caused by deletion of seven amino acids at the juxtamembrane domain
1996
Isolated familial pheochromocytoma as a variant of von Hippel-Lindau disease.
1996
Fas Preassociation Required for Apoptosis Signaling and Dominant Inhibition by Pathogenic Mutations
2000 StandoutScienceNobel
Reactive oxygen species are critical for the growth and differentiation of medullary thyroid carcinoma cells.
2000
Human Cancer Syndromes: Clues to the Origin and Nature of Cancer
1997 Science
Systematic Review of Microsatellite Instability and Colorectal Cancer Prognosis
2005
Notch Signaling: Cell Fate Control and Signal Integration in Development
1999 StandoutScience
Effector Memory T Cells, Early Metastasis, and Survival in Colorectal Cancer
2005 Standout
Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas.
1995
Structural Dynamics of Eukaryotic Chromosome Evolution
2003 StandoutScience
Diversity and frequency of epidermal growth factor receptor mutations in human glioblastomas.
2000
Human Homolog of patched , a Candidate Gene for the Basal Cell Nevus Syndrome
1996 StandoutScience
Free Radicals in the Physiological Control of Cell Function
2002 Standout
Role ofVHLGene Mutation in Human Cancer
2004 StandoutNobel
Mutations in the Extracellular Domain Cause RET Loss of Function by a Dominant Negative Mechanism
1998
The Human Genome Project: Reaching the Finish Line
1998 StandoutScienceNobel
Genetic Testing for Cancer Predisposition
2001
Pheochromocytoma and Paraganglioma: An Endocrine Society Clinical Practice Guideline
2014 Standout
Works of Laura Papi being referenced
Dinucleotide repeat polymorphism at the RBP3 locus in chromosome band 10q11.2
1992
Evidence of a four-hit mechanism involvingSMARCB1andNF2in schwannomatosis-associated schwannomas
2007
Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2
1993
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
1993 Nature
Microsatellite instability in sporadic mucinous colorectal carcinomas: relationship to clinico-pathological variables
1997
The neurofibromatosis type 2 gene is inactivated in schwannomas
1994
Duplicated KOX zinc finger gene clusters flank the centromere of human chromosome 10: evidence for a pericentric inversion during primate evolution
1993
Prognostic significance of microsatellite instability in sporadic mucinous colorectal cancers
1999
Update from the 2011 International Schwannomatosis Workshop: From genetics to diagnostic criteria
2013
Types, stability, and phenotypic consequences of chromosome rearrangements leading to interstitial telomeric sequences.
1993
Microsatellite instability in sporadic mucinous colorectal carcinomas: relationship to clinico‐pathological variables
1997