Riccardo Fodde
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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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(Suggest an Edit or Addition)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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