Riccardo Fodde

Q: What Schools Are Affiliated With Riccardo Fodde

Riccardo Fodde is affiliated with the following schools: University of Amsterdam, University of Milan, University of Groningen, Leiden University

Riccardo Fodde's AcademicInfluence.com Rankings

Riccardo Fodde

Computer Science

#9066

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#9525

Historical Rank

Computational Linguistics

#2131

World Rank

#2153

Historical Rank

Machine Learning

#3878

World Rank

#3924

Historical Rank

Artificial Intelligence

#4205

World Rank

#4263

Historical Rank

computer-science Degrees

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Computer Science

Riccardo Fodde's Degrees

PhD Computer Science University of Milan
Masters Computer Science University of Milan
Bachelors Computer Science University of Milan

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Riccardo Fodde's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer. (1998) (4146)
APC, Signal transduction and genetic instability in colorectal cancer (2001) (975)
Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis. (1996) (869)
Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial (2011) (826)
Mutations in the APC tumour suppressor gene cause chromosomal instability (2001) (755)
Wnt/β-catenin signaling in cancer stemness and malignant behavior (2007) (692)
A targeted chain-termination mutation in the mouse Apc gene results in multiple intestinal tumors. (1994) (578)
CCAT2, a novel noncoding RNA mapping to 8q24, underlies metastatic progression and chromosomal instability in colon cancer (2013) (574)
Expression of CD44 in Apc and Tcf mutant mice implies regulation by the WNT pathway. (1999) (551)
Wnt/beta-catenin signaling in cancer stemness and malignant behavior. (2007) (493)
Familial endometrial cancer in female carriers of MSH6 germline mutations (1999) (465)
Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance. (2004) (437)
Clinical findings with implications for genetic testing in families with clustering of colorectal cancer. (1998) (410)
The APC gene in colorectal cancer. (2002) (384)
The 'just-right' signaling model: APC somatic mutations are selected based on a specific level of activation of the beta-catenin signaling cascade. (2002) (377)
Apc modulates embryonic stem-cell differentiation by controlling the dosage of β-catenin signaling (2002) (362)
Interplay between metabolic identities in the intestinal crypt supports stem cell function (2017) (313)
Canonical wnt signaling regulates hematopoiesis in a dosage-dependent fashion. (2011) (301)
Junk DNA and the long non-coding RNA twist in cancer genetics (2015) (280)
Apc1638T: a mouse model delineating critical domains of the adenomatous polyposis coli protein involved in tumorigenesis and development. (1999) (258)
MSH2 genomic deletions are a frequent cause of HNPCC (1998) (246)
Wnt signaling inhibits osteogenic differentiation of human mesenchymal stem cells. (2004) (236)
The CHEK2 1100delC mutation identifies families with a hereditary breast and colorectal cancer phenotype. (2003) (226)
Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations. (1997) (219)
Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene. (2003) (218)
Rapid detection of translation-terminating mutations at the adenomatous polyposis coli (APC) gene by direct protein truncation test. (1994) (212)
Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP) (2005) (209)
cAMP/PKA pathway activation in human mesenchymal stem cells in vitro results in robust bone formation in vivo (2008) (202)
Mutation detection by denaturing gradient gel electrophoresis (DGGE) (1994) (192)
APC and oncogenic KRAS are synergistic in enhancing Wnt signaling in intestinal tumor formation and progression. (2006) (192)
A Randomized Placebo-Controlled Prevention Trial of Aspirin and/or Resistant Starch in Young People with Familial Adenomatous Polyposis (2011) (191)
Conventional and tissue microarray immunohistochemical expression analysis of mismatch repair in hereditary colorectal tumors. (2003) (190)
Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene. (1996) (189)
Cancer stemness and metastasis: therapeutic consequences and perspectives. (2010) (182)
CCAT2, a novel long non-coding RNA in breast cancer: expression study and clinical correlations (2013) (181)
Phenotypic and genotypic heterogeneity in the Lynch syndrome: diagnostic, surveillance and management implications (2006) (177)
Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree (2001) (177)
Effect of aspirin or resistant starch on colorectal neoplasia in the Lynch syndrome. (2008) (172)
Role of CLASP2 in Microtubule Stabilization and the Regulation of Persistent Motility (2006) (171)
Germline mutations in the 3′ part of APC exon 15 do not result in truncated proteins and are associated with attenuated adenomatous polyposis coli (1996) (157)
Use of Aspirin postdiagnosis improves survival for colon cancer patients (2012) (154)
Paneth Cells in Intestinal Homeostasis and Tissue Injury (2012) (149)
Apc1638N: a mouse model for familial adenomatous polyposis-associated desmoid tumors and cutaneous cysts. (1998) (141)
Molecular analysis of the APC gene in 105 Dutch kindreds with familial adenomatous polyposis: 67 germline mutations identified by DGGE, PTT, and southern analysis (1997) (141)
β-catenin tyrosine 654 phosphorylation increases Wnt signalling and intestinal tumorigenesis (2011) (140)
Expression and genomic profiling of colorectal cancer. (2007) (139)
APC dosage effects in tumorigenesis and stem cell differentiation. (2004) (138)
A Matter of Dosage (2002) (138)
Paneth Cells Respond to Inflammation and Contribute to Tissue Regeneration by Acquiring Stem-like Features through SCF/c-Kit Signaling. (2018) (138)
Denaturing gradient gel electrophoresis and direct sequencing of PCR amplified genomic DNA: a rapid and reliable diagnostic approach to beta thalassaemia (1990) (133)
Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16. (1996) (132)
Long-term effect of resistant starch on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial. (2012) (129)
Loss of Apc and the entire chromosome 18 but absence of mutations at the Ras and Tp53 genes in intestinal tumors from Apc1638N, a mouse model for Apc-driven carcinogenesis. (1997) (128)
Molecular characterization of the spectrum of genomic deletions in the mismatch repair genes MSH2, MLH1, MSH6, and PMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC) (2005) (126)
Wnt Signaling in Ovarian Cancer Stemness, EMT, and Therapy Resistance (2019) (120)
Cancer stem cells and metastasis. (2012) (119)
Progesterone Inhibition of Wnt/β-Catenin Signaling in Normal Endometrium and Endometrial Cancer (2009) (119)
Eight novel inactivating germ line mutations at the APC gene identified by denaturing gradient gel electrophoresis. (1992) (118)
Base transitions are the most frequent genetic changes at P53 in gastric cancer. (1993) (114)
APC and Oncogenic KRAS Are Synergistic in Enhancing Wnt Signaling in Intestinal Tumor Formation and Progression (2006) (110)
Cyclooxygenase-two (COX-2) modulates proliferation in aggressive fibromatosis (desmoid tumor) (2001) (108)
Somatic Apc mutations are selected upon their capacity to inactivate the β‐catenin downregulating activity (2000) (103)
Wnt/Β-Catenin and Sex Hormone Signaling In Endometrial Homeostasis and Cancer (2010) (103)
Genetic deletion of receptor for hyaluronan-mediated motility (Rhamm) attenuates the formation of aggressive fibromatosis (desmoid tumor) (2003) (102)
Tumour–stroma interactions in colorectal cancer: converging on β-catenin activation and cancer stemness (2008) (100)
Somatic acquisition and signaling of TGFBR1*6A in cancer. (2005) (99)
Disease model: familial adenomatous polyposis. (2001) (98)
Expression of HLA class I antigen, aspirin use, and survival after a diagnosis of colon cancer. (2014) (94)
A germline mutation at the extreme 3′ end of the APC gene results in a severe desmoid phenotype and is associated with overexpression of beta‐catenin in the desmoid tumor (2000) (90)
APC mutation in the alternatively spliced region of exon 9 associated with late onset familial adenomatous polyposis (1995) (89)
Cross-species comparison of human and mouse intestinal polyps reveals conserved mechanisms in adenomatous polyposis coli (APC)-driven tumorigenesis. (2008) (85)
Concepts of metastasis in flux: the stromal progression model. (2012) (83)
Wnt Signaling Regulates the Lineage Differentiation Potential of Mouse Embryonic Stem Cells through Tcf3 Down-Regulation (2013) (82)
Chromosomal instability in MYH- and APC-mutant adenomatous polyps. (2006) (80)
A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United States. (2004) (79)
A mouse model of human familial adenomatous polyposis. (1997) (79)
A Targeted Constitutive Mutation in the Apc Tumor Suppressor Gene Underlies Mammary But Not Intestinal Tumorigenesis (2009) (79)
Leiden open variation database of the MUTYH gene (2010) (77)
The multiple functions of tumour suppressors: it's all in APC (2003) (76)
Prostate cancer is part of the hereditary non‐polyposis colorectal cancer (HNPCC) tumor spectrum (2003) (75)
A new conditional Apc-mutant mouse model for colorectal cancer. (2010) (74)
Smad4 haploinsufficiency in mouse models for intestinal cancer (2006) (74)
Secreted Phospholipases A2 Are Intestinal Stem Cell Niche Factors with Distinct Roles in Homeostasis, Inflammation, and Cancer. (2016) (74)
Morphological changes in tumour type after radiotherapy are accompanied by changes in gene expression profile but not in clinical behaviour (2004) (72)
IL6/JAK1/STAT3 Signaling Blockade in Endometrial Cancer Affects the ALDHhi/CD126+ Stem-like Component and Reduces Tumor Burden. (2015) (71)
EXO1 variants occur commonly in normal population: evidence against a role in hereditary nonpolyposis colorectal cancer. (2003) (70)
Comprehensive genetic analysis of relevant four genes in 49 patients with Marfan syndrome or Marfan‐related phenotypes (2006) (70)
Identification of Quiescent, Stem-Like Cells in the Distal Female Reproductive Tract (2012) (66)
A 10‐Mb paracentric inversion of chromosome arm 2p inactivates MSH2 and is responsible for hereditary nonpolyposis colorectal cancer in a North‐American kindred (2002) (63)
A targeted mouse Brca1 mutation removing the last BRCT repeat results in apoptosis and embryonic lethality at the headfold stage (2001) (62)
Genotype-phenotype correlations at the adenomatous polyposis coli (APC) gene. (1995) (62)
The involvement of Alu repeats in recombination events at the α-globin gene cluster: characterization of two α°-thalassaemia deletion breakpoints (1997) (62)
Adenomatous polyposis coli-mediated control of β-catenin is essential for both chondrogenic and osteogenic differentiation of skeletal precursors (2009) (60)
Colorectal cancers show distinct mutation spectra in members of the canonical WNT signaling pathway according to their anatomical location and type of genetic instability (2010) (58)
E-cadherin and adenomatous polyposis coli mutations are synergistic in intestinal tumor initiation in mice. (2000) (57)
Alterations in Wnt–β‐catenin and Pten signalling play distinct roles in endometrial cancer initiation and progression (2013) (57)
Intestinal tumorigenesis in the Apc1638N mouse treated with aspirin and resistant starch for up to 5 months. (1999) (57)
Severe Alterations of Cerebellar Cortical Development after Constitutive Activation of Wnt Signaling in Granule Neuron Precursors (2011) (56)
CA repeat polymorphism at the D5S82 locus, proximal to adenomatous polyposis coli (APC). (1991) (55)
CA repeat polymorphism at the D5S299 locus linked to adenomatous polyposis coli (APC). (1991) (55)
Genomic profiling by DNA amplification of laser capture microdissected tissues and array CGH. (2004) (54)
Apc modulates embryonic stem-cell differentiation by controlling the dosage of β-catenin signaling (2003) (53)
TGFBR1*6A may contribute to hereditary colorectal cancer. (2005) (52)
Cancer-associated rs6983267 SNP and its accompanying long noncoding RNA CCAT2 induce myeloid malignancies via unique SNP-specific RNA mutations (2018) (51)
High Levels of Canonical Wnt Signaling Lead to Loss of Stemness and Increased Differentiation in Hematopoietic Stem Cells (2016) (51)
Premature chromosome condensation revisited: A novel chemical approach permits efficient cytogenetic analysis of cancers (2003) (51)
Inclusion of malignant fibrous histiocytoma in the tumour spectrum associated with hereditary non‐polyposis colorectal cancer (2000) (50)
Wnt pathway-related gene expression during malignant progression in ulcerative colitis. (2007) (48)
DOC1-Dependent Recruitment of NURD Reveals Antagonism with SWI/SNF during Epithelial-Mesenchymal Transition in Oral Cancer Cells. (2017) (44)
Cancer stemness in Wnt-driven mammary tumorigenesis. (2014) (44)
Proximal Fluid Proteome Profiling of Mouse Colon Tumors Reveals Biomarkers for Early Diagnosis of Human Colorectal Cancer (2012) (44)
Nuclear β‐catenin expression and Wnt signalling: in defence of the dogma (2010) (44)
Cancer stem cells, pluripotency, and cellular heterogeneity: a WNTer perspective. (2014) (43)
Serrated adenomas and mixed polyposis caused by a splice acceptor deletion in the mouse Smad4 gene (2003) (43)
Detection of mutations in mismatch repair genes in Portuguese families with hereditary non-polyposis colorectal cancer (HNPCC) by a multi-method approach (2000) (43)
Genetic evidence that Turcot syndrome is not allelic to familial adenomatous polyposis. (1992) (41)
Prevalence of adenomas and hyperplastic polyps in mismatch repair mutation carriers among CAPP2 participants: report by the colorectal adenoma/carcinoma prevention programme 2. (2008) (41)
Dynamic expression and nuclear accumulation of β-catenin during the development of hair follicle-derived structures (2001) (40)
Matrix Metalloproteinase Activity Modulates Tumor Size, Cell Motility, and Cell Invasiveness in Murine Aggressive Fibromatosis (2004) (40)
Protective effect of nonsteroidal anti-inflammatory drugs on colorectal adenomas is modified by a polymorphism in peroxisome proliferator-activated receptor δ (2006) (39)
The inflammatory cytokine IL-6 induces FRA1 deacetylation promoting colorectal cancer stem-like properties (2019) (38)
Cell Heterogeneity and Phenotypic Plasticity in Metastasis Formation: The Case of Colon Cancer (2019) (37)
Intestinal and extra-intestinal tumor multiplicities in the Apc1638N mouse model after exposure to X-rays. (1997) (37)
A nonsense mutation in MLH1 causes exon skipping in three unrelated HNPCC families. (2001) (36)
Carrier risk status changes resulting from mutation testing in hereditary non-polyposis colorectal cancer and hereditary breast-ovarian cancer (2003) (36)
Detection of K-ras mutations by denaturing gradient gel electrophoresis (DGGE): a study on pancreatic cancer. (1992) (36)
The role of the APC tumor suppressor in chromosomal instability. (2006) (34)
Molecular, cytogenetic, and phenotypic studies of a constitutional reciprocal translocation t(5; I0)(q22; q25) responsible for familial adenomatous polyposis in a Dutch pedigree (1995) (33)
Automated acquisition of stained tissue microarrays for high-throughput evaluation of molecular targets. (2003) (32)
The genetic background modifies the spontaneous and X‐ray–induced tumor spectrum in the Apc1638N mouse model (1999) (32)
SET-CAN, the product of the t(9;9) in acute undifferentiated leukemia, causes expansion of early hematopoietic progenitors and hyperproliferation of stomach mucosa in transgenic mice. (2007) (32)
Spectrum of genetic alterations in Muir‐Torre syndrome is the same as in HNPCC (2004) (31)
Mechanisms of APC-driven tumorigenesis: lessons from mouse models (1999) (31)
Familial Adenomatous Polyposis-Associated Desmoids Display Significantly More Genetic Changes than Sporadic Desmoids (2011) (31)
Barrett's oesophageal adenocarcinoma encompasses tumour‐initiating cells that do not express common cancer stem cell markers (2010) (29)
Smad4 haploinsufficiency: a matter of dosage (2008) (28)
Prevalence and molecular heterogeneity of alfa+thalassemia in two tribal populations from Andhra Pradesh, India (1988) (27)
Rapid identification by denaturing gradient gel electrophoresis of mutations in the γ‐globin gene promoters in non‐deletion type HPFH (1992) (27)
Familial adenomatous polyposis associated with multiple adrenal adenomas in a patient with a rare 3′ APC mutation (1999) (27)
The involvement of Alu repeats in recombination events at the alpha-globin gene cluster: characterization of two alphazero-thalassaemia deletion breakpoints. (1997) (25)
Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer (2016) (25)
CA repeat polymorphism within the MCC (mutated in colorectal cancer) gene. (1991) (24)
Quiescent stem cells in intestinal homeostasis and cancer (2011) (24)
Targeted deletion of the C-terminus of the mouse adenomatous polyposis coli tumor suppressor results in neurologic phenotypes related to schizophrenia (2014) (24)
Of mice and (wo)men: genotype-phenotype correlations in BRCA1. (2003) (23)
CA repeat polymorphism from YAC JW25 at the D5S318 locus, distal to adenomatous polyposis coli (APC). (1991) (23)
Aneuploidy arises at early stages of Apc-driven intestinal tumorigenesis and pinpoints conserved chromosomal loci of allelic imbalance between mouse and human. (2007) (23)
Rapidly progressive adenomatous polyposis in a patient with germline mutations in both the APC and MLH1 genes: the worst of two worlds (2003) (21)
Radiation induces different changes in expression profiles of normal rectal tissue compared with rectal carcinoma (2005) (21)
Involvement of MBD4 inactivation in mismatch repair-deficient tumorigenesis (2015) (21)
Generation of a tightly regulated doxycycline‐inducible model for studying mouse intestinal biology (2009) (21)
Homozygous beta+ thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human beta globin gene. (1991) (20)
Phenotypic plasticity underlies local invasion and distant metastasis in colon cancer (2021) (20)
Nucleotide sequence of the Belgian G gamma+(A gamma delta beta)0-thalassemia deletion breakpoint suggests a common mechanism for a number of such recombination events. (1990) (19)
A Founder Mutation of the MSH 2 Gene and Hereditary Nonpolyposis Colorectal Cancer in the United States (2004) (19)
American founder mutation for Lynch syndrome (2006) (16)
Short-term carcinogenicity testing of a potent murine intestinal mutagen, 2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine (PhIP), in Apc1638N transgenic mice. (1997) (16)
AT repeat polymorphism at the D5S122 locus tightly linked to adenomatous polyposis coli (APC). (1991) (16)
Multiple Primary Cancer, Including Transitional Cell Carcinoma of the Upper Uroepithelial Tract in a Multigeneration HNPCC Family: Molecular Genetic, Diagnostic, and Management Implications (2003) (16)
The stem of cancer. (2009) (16)
Prediction of the outcome of genetic testing in HNPCC kindreds using the revised Amsterdam criteria and immunohistochemistry (2004) (16)
DGGE polymorphism in intron 10 of MSH2, the HNPCC gene. (1994) (16)
Erratum: Apc modulates embryonic stem-cell differentiation by controlling the dosage of β-catenin signaling (Nature Genetics (2002) 32 (594-605)) (2003) (15)
Loss of APC function in mesenchymal cells surrounding the Müllerian duct leads to myometrial defects in adult mice (2011) (15)
Evidence for Msh2 haploinsufficiency in mice revealed by MNU-induced sister-chromatid exchange analysis (2000) (15)
Multiple recombination events are responsible for the heterogeneity of α+‐thalassemia haplotypes among the forest tribes of Andhra Pradesh, India (1991) (15)
Germline APC mutation familial adenomatous polyposis in Indian family (1992) (15)
Rapid detection of polymorphism near gene for adult polycystic kidney disease (1990) (15)
EXO 1 Variants Occur Commonly in Normal Population : Evidence against a Role in Hereditary Nonpolyposis Colorectal Cancer 1 (2002) (14)
Rapid detection of the highly polymorphic beta globin framework by denaturing gradient gel electrophoresis. (1992) (13)
Interaction of two different disorders in the beta-globin gene cluster associated with an increased hemoglobin F production: a novel deletion type of (G) gamma + ((A) gamma delta beta)(0)-thalassemia and a delta(0)-hereditary persistence of fetal hemoglobin determinant. (1991) (13)
CD24 Is Not Required for Tumor Initiation and Growth in Murine Breast and Prostate Cancer Models (2016) (13)
Expression analysis of proline rich 15 (Prr15) in mouse and human gastrointestinal tumors (2011) (13)
Sites and types of p53 mutations in an unselected series of colorectal cancers in The Netherlands. (1993) (12)
Genetic analysis of a breast–ovarian cancer family, with 7 cases of colorectal cancer linked to BRCA1, fails to support a role for BRCA1 in colorectal tumorigenesis (2000) (12)
The role of S100a4 (Mts1) in Apc- and Smad4-driven tumour onset and progression. (2016) (11)
DOC 1-Dependent Recruitment of NURD Reveals Antagonism with SWI / SNF during Epithelial-Mesenchymal Transition in Oral Cancer Cells (2017) (11)
[Genetics of colorectal cancer. I. Non-polyposis and polyposis forms of hereditary colorectal cancer]. (1999) (11)
A novel delta zero-thalassemia arising from a frameshift insertion, detected by direct sequencing of enzymatically amplified DNA. (1989) (11)
Stem Cells and Metastatic Cancer: Fatal Attraction? (2006) (11)
Homology of a 130-kb region enclosing the α-globin gene cluster, the α-locus controlling region, and two non-globin genes in human and mouse (2004) (10)
The C-terminal domain of the adenomatous polyposis coli (Apc) protein is involved in thyroid morphogenesis and function (2011) (9)
Cancer Stemness in Apc- vs. Apc/KRAS-Driven Intestinal Tumorigenesis (2013) (9)
Functional interaction between PKA and BM? Signaling during osteogenic differentiation of human mesenchymal stem cells. (2005) (9)
Mapping of two new markers within the smallest interval harboring the spinal muscular atrophy locus by family and radiation hybrid analysis (1994) (8)
HB J-Anatolia [α61(E10)LYSTHR]: Structural Characterization and Gene Localization of A New a Chain Variant (1990) (8)
Results of the CAPP1 Study: aspirin and resistant starch are beneficial in familial adenomatous polyposis (2003) (8)
MicroRNA-135b and its circuitry networks as potential therapeutic targets in colon cancer (2013) (8)
C-Terminal Phosphorylation of β-Catenin Increases Wnt Signaling and Intestinal Tumorigenesis (2011) (7)
[Genetics of colorectal cancer. II. Hereditary background of sporadic and familial colorectal cancer]. (1999) (7)
Fibroblast activation protein identifies Consensus Molecular Subtype 4 in colorectal cancer and allows its detection by 68Ga-FAPI-PET imaging (2022) (6)
Erratum: Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis (Gastroenterology (1996) 110 (1020- 1027)) (1996) (6)
Ectopic activation of WNT signaling in human embryonal carcinoma cells and its effects in short- and long-term in vitro culture (2019) (6)
A novel δ° arising from a frameshift insertion, detected by direct sequencing of enzymatically amplified DNA (1989) (6)
Mutation Analysis by Denaturing Gradient Gel Electrophoresis (DGGE) (1996) (4)
The nature of intestinal stem cells' nurture (2011) (4)
Marfan-like habitus and familial adenomatous polyposis in two unrelated males: a significant association? (1999) (4)
Some fine-structural findings on the thyroid gland in Apc1638T/1638T mice that express a C-terminus lacking truncated Apc (2012) (4)
A Novel Frameshift Mutation [FSC 47 (+A)] Causing β-Thalassemia in a Surinam Patient (1990) (3)
The Organoid Reconstitution Assay (ORA) for the Functional Analysis of Intestinal Stem and Niche Cells. (2017) (3)
T1768 Generation of a Tightly Regulated Doxycycline-Inducible Model for Studying Mouse Intestinal Biology (2009) (3)
Early morbidity encountered in the dietary-related mouse model of Barrett's esophagus: a question of zinc? (2011) (3)
Long-term effect of resistant starch on cancer risk in carriers of hereditary colorectal cancer (2016) (3)
p53 mutations in colorectal cancers in the patients of Metropolitan New York. (1993) (3)
Multitasking Paneth Cells in the Intestinal Stem Cell Niche (2018) (2)
Modelling western dietary habits in the mouse: easier said than done. (2017) (2)
Generation and characterization of an inducible transgenic model for studying mouse esophageal biology (2012) (2)
Colonoscopic screening of carriers of mismatch repair gene mutations: Results from the Dutch HNPCC registry. (2000) (2)
Genotype-Phenotype Correlations in Intestinal Carcinogenesis: Lessons From Mouse Models (1996) (2)
APC-mutant cells exploit compensatory chromosome alterations to restore tumour cell fitness (2020) (1)
Generation and characterization of an inducible transgenic model for studying mouse esophageal biology (2012) (1)
12 DOC1-dependent recruitment of NURD reveals antagonism with SWI/SNF during epithelial-mesenchymal transition in oral cancer cells (2018) (1)
An update of cancer risk in HNPCC: A study of 101 families including 58 families associated with mismatch repair mutations (2000) (1)
The American founder mutation for Lynch syndrome: Prevalence and cancer control implications (2005) (1)
A Founder Mutation of theMSH2 Gene and Hereditary Nonpolyposis Colorectal Cancer in the United States (2004) (1)
Homozygous + thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human globin gene (1)
Long Non-Coding RNA Induces De Novo Myelodysplastic Syndrome through Epigenetic Regulation (2015) (1)
Hb J-Anatolia [alpha 61(E10)Lys----Thr]: structural characterization and gene localization of a new alpha chain variant. (1990) (1)
Dinucleotide repeat polymorphism proximal to the spinal muscular atrophy region at the D5S524 locus. (1993) (1)
Isolation and characterization of novel genes responsible for hereditary non-polyposis colorectal cancer (HNPCC). (1999) (0)
Embryonic lethality in the Brca1-1700T mouse model suggests inhibition of p53-dependent pathways (2000) (0)
40 The Role of Tyrosine 654 Phosphorylated β-Catenin in Intestinal Tumor Formation (2009) (0)
Paneth cells as the origin of intestinal cancer in the context of inflammation (2023) (0)
28 INVITED Wnt/beta catenin signaling in intestinal and mammary cancer stemness (2007) (0)
Endometrioid Ovarian Cancer and Endometriosis Originate from the Distal Oviduct. Conditional Activation of Wnt/beta-Catenin Signaling in Mullerian Duct Derived Organs (2013) (0)
Effect of protein kinase A on osteogenic differentiation and in vivo bone formation by human mesenchymal stem cells (2005) (0)
The long term impact of resistant starch on cancer risk in carriers of hereditary colorectal cancer:the CAPP2 Randomised Controlled Trial (2012) (0)
Cross-talk of sexhormones and Wnt/ß-catenin signaling in endometrial cancer (2005) (0)
A new Avall RFLP in the human α-globin gene cluster (1990) (0)
Abstract 4208: Constitutive activation of Wnt/beta-catenin signaling induces uterine developmental defects (2010) (0)
Adenomatous polyposis coli-gene dosage controls β-catenin-mediated differentia- tion of skeletal precursors (2011) (0)
[Hemoglobinopathies, screening and molecular-genetic studies in foreign women in The Netherlands]. (1992) (0)
Correction: Teeuwssen and Fodde; Colon Cancer Heterogeneity and Phenotypic Plasticity in Metastasis Formation. Cancers 2019, 11(9), 1368 (2020) (0)
Abstracts presented at the XVIth symposium of The Netherlands Foundation for the Detection of Hereditary Tumours, 'New Developments in Hereditary Cancer', 31 January 2003, Utrecht, The Netherlands (2004) (0)
Moleculaire classificatie van familiale colorectale kanker door middel van weefsel- en cDNA microarray-analyse (2001) (0)
Rapid detection of APC mutations in FAP families and colorectal tumors by protein truncation test (1994) (0)
A novel frameshift mutation [FSC 47 (+A)] causing beta-thalassemia in a Surinam patient. (1990) (0)
Abstract C6: Barrett's esophagus and esophageal adenocarcinoma: A paradigm for the cancer stem cell model? (2009) (0)
Author response: Phenotypic plasticity underlies local invasion and distant metastasis in colon cancer (2021) (0)
Abstracts presented at the XVth Symposium of the NetherlandsFoundation for the Detection of Hereditary Tumours,1 February 2002, Utrecht, The Netherlands (2004) (0)
Quiescent stem cells in intestinal homeostasis, inflammation, and cancer (2011) (0)
Wnt Signaling in Adult Stem Cells (2014) (0)
Rapiddetection ofthehighly polymorphic globin framework bydenaturing gradient gel electrophoresis (1992) (0)
The role of the adenomatous polyposis coli (APC) protein in neural differentiation (2000) (0)
TWO Multitasking Paneth Cells in the Intestinal Stem Cell Niche (2018) (0)
Alternative splicing downstream of EMT enhances phenotypic plasticity and malignant behavior in colon cancer (2022) (0)
6157 POSTER Use of Aspirin Postdiagnosis Improves Survival for Colon Cancer Patients (2011) (0)
APC Gene in Familial Adenomatous Polyposis (2015) (0)
A new AvaII RFLP in the human alpha-globin gene cluster. (1990) (0)
Functional analysis of BRCA1 in breast cancer development (2001) (0)
Targeted deletion of the C-terminus of the mouse adenomatous polyposis coli tumor suppressor results in neurologic phenotypes related to schizophrenia (2014) (0)
Carcinomas of the digestive tract (2008) (0)
Molecular classification of familial colorectal cancer by tissue and cDNA microarray analysis (2001) (0)
Influence of intestinal flora on the development of adenomas in the APC1638N mouse (1999) (0)
FAP and Marfanoid habitus (2000) (0)
PG 3.01 Cancer stem cells: the new target (2012) (0)
68 CCAT2 LNCRNA INDUCES DE NOVO MYELODYSPLASTIC SYNDROME IN VIVO (2015) (0)
Cross-talk between receptor tyrosine kinases and ß-catenin signaling during tumor initiation and progression (2004) (0)
Dialoog tussen receptor tyrosine kinases en beta-catenine signalering gedurende de initiatie en verdere ontwikkeling van tumoren (2004) (0)
The co-activators of de-regulated Wnt/ß-catenin signaling, BCL9-2 and Pygo2, are potential targets for colon cancer therapy (2016) (0)
Microarray analysis of factors determining apoptosis in human rectal cancers (2002) (0)
Adenomatous polyposis coli-mediated control of β-catenin is essential for both chondrogenic and osteogenic differentia- tion of skeletal precursors (2011) (0)
Abstracts Presented at the XVIIth Symposium ‘New Developments in Hereditary Cancer’, 5–6 February 2004, Amsterdam, the Netherlands (2004) (0)
Phenotypic plasticity and partial EMT underlie local invasion and distant metastasis in colon cancer (2020) (0)
cancer metastatic progression and chromosomal instability in colon , a novel noncoding RNA mapping to 8 q 24 , underlies CCAT 2 Material Supplemental (2013) (0)
Su1876 Proximal Fluid Proteome Profiling of Mouse Colon Tumors Reveals Biomarkers for Early Diagnosis of Human Colorectal Cancer (2012) (0)
Lynch syndrome founder mutations in families of Navajo and German-American heritage. (2004) (0)
An update of cancer risk in HNPCC (2000) (0)
Neoplastic lesions and chronic inflammation of the gastrointestinal tract (2010) (0)

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