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Paul Goodfellow

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Hill D Ashley; Ivanovich Jennifer; Priest John R; Gurnett Christina A; Dehner Louis P; Desruisseau David; Jarzembowski Jason A; Wikenheiser-Brokamp Kathryn A; Suarez Brian K; Whelan Alison J; Williams Gretchen; Bracamontes Dawn; Messinger Yoav; Goodfellow Paul J
DICER1 mutations in familial pleuropulmonary blastoma.
Varley Katherine E; Mutch David G; Edmonston Tina B; Goodfellow Paul J; Mitra Robi D
Intra-tumor heterogeneity of MLH1 promoter methylation revealed by deep single molecule bisulfite sequencing.
Zighelboim Israel; Schmidt Amy P; Gao Feng; Thaker Premal H; Powell Matthew A; Rader Janet S; Gibb Randall K; Mutch David G; Goodfellow Paul J
ATR mutation in endometrioid endometrial cancer is associated with poor clinical outcomes.

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All Publications

2009: Hill D Ashley; Ivanovich Jennifer; Priest John R; Gurnett Christina A; Dehner Louis P; Desruisseau David; Jarzembowski Jason A; Wikenheiser-Brokamp Kathryn A; Suarez Brian K; Whelan Alison J; Williams Gretchen; Bracamontes Dawn; Messinger Yoav; Goodfellow Paul J
DICER1 mutations in familial pleuropulmonary blastoma.
Science (New York, N.Y.) 2009;325(5943):965.
2009: Varley Katherine E; Mutch David G; Edmonston Tina B; Goodfellow Paul J; Mitra Robi D
Intra-tumor heterogeneity of MLH1 promoter methylation revealed by deep single molecule bisulfite sequencing.
Nucleic acids research 2009;37(14):4603-12.
2009: Zighelboim Israel; Schmidt Amy P; Gao Feng; Thaker Premal H; Powell Matthew A; Rader Janet S; Gibb Randall K; Mutch David G; Goodfellow Paul J
ATR mutation in endometrioid endometrial cancer is associated with poor clinical outcomes.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2009;27(19):3091-6.
2009: Goodfellow Paul J
Clinicopathologic significance of DNA mismatch repair defects in endometrial cancer: the devil is in the details.
Gynecologic oncology 2009;113(2):151-2.
2009: Rimel B J; Huettner Phyllis; Powell Matthew A; Mutch David G; Goodfellow Paul J
Absence of MGMT promoter methylation in endometrial cancer.
Gynecologic oncology 2009;112(1):224-8.
2009: Zighelboim Israel; Powell Matthew A; Babb Sheri A; Whelan Alison J; Schmidt Amy P; Clendenning Mark; Senter Leigha; Thibodeau Stephen N; de la Chapelle Albert; Goodfellow Paul J
Epitope-positive truncating MLH1 mutation and loss of PMS2: implications for IHC-directed genetic testing for Lynch syndrome.
Familial cancer 2009;8(4):501-4.
2008: Byron Sara A; Gartside Michael G; Wellens Candice L; Mallon Mary A; Keenan Jack B; Powell Matthew A; Goodfellow Paul J; Pollock Pamela M
Inhibition of activated fibroblast growth factor receptor 2 in endometrial cancer cells induces cell death despite PTEN abrogation.
Cancer research 2008;68(17):6902-7.
2008: Case Ashley S; Zighelboim Israel; Mutch David G; Babb Sheri A; Schmidt Amy P; Whelan Alison J; Thibodeau Stephen N; Goodfellow Paul J
Clustering of Lynch syndrome malignancies with no evidence for a role of DNA mismatch repair.
Gynecologic oncology 2008;108(2):438-44.
2007: Pollock P M; Gartside M G; Dejeza L C; Powell M A; Mallon M A; Davies H; Mohammadi M; Futreal P A; Stratton M R; Trent J M; Goodfellow P J
Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes.
Oncogene 2007;26(50):7158-62.
2007: Zighelboim Israel; Goodfellow Paul J; Gao Feng; Gibb Randall K; Powell Matthew A; Rader Janet S; Mutch David G
Microsatellite instability and epigenetic inactivation of MLH1 and outcome of patients with endometrial carcinomas of the endometrioid type.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2007;25(15):2042-8.
2007: Zighelboim Israel; Goodfellow Paul J; Schmidt Amy P; Walls Ken C; Mallon Mary Ann; Mutch David G; Yan Pearlly S; Huang Tim Hui-Ming; Powell Matthew A
Differential methylation hybridization array of endometrial cancers reveals two novel cancer-specific methylation markers.
Clinical cancer research : an official journal of the American Association for Cancer Research 2007;13(10):2882-9.
2007: Zighelboim Israel; Babb Sheri; Gao Feng; Powell Matthew A; Mutch David G; Goodfellow Paul J
Excess of early onset multiple myeloma in endometrial cancer probands and their relatives suggests common susceptibility.
Gynecologic oncology 2007;105(2):390-4.
2007: Chen Huiping; Taylor Nicholas P; Sotamaa Kaisa M; Mutch David G; Powell Matthew A; Schmidt Amy P; Feng Sheng; Hampel Heather L; de la Chapelle Albert; Goodfellow Paul J
Evidence for heritable predisposition to epigenetic silencing of MLH1.
International journal of cancer. Journal international du cancer 2007;120(8):1684-8.
2007: McCourt Carolyn K; Mutch David G; Gibb Randall K; Rader Janet S; Goodfellow Paul J; Trinkaus Kathryn; Powell Matthew A
Body mass index: relationship to clinical, pathologic and features of microsatellite instability in endometrial cancer.
Gynecologic oncology 2007;104(3):535-9.
2006: Buttin B M; Powell M A; Goodfellow P J; Lewin S N; Gibb R K; Mutch D G
Increased risk for abnormalities on perioperative colon screening in patients with microsatellite instability-positive endometrial carcinoma.
International journal of gynecological cancer : official journal of the International Gynecological Cancer Society 2006;16(6):1980-6.
2006: Taylor Nicholas P; Zighelboim Israel; Huettner Phyllis C; Powell Matthew A; Gibb Randall K; Rader Janet S; Mutch David G; Edmonston Tina B; Goodfellow Paul J
DNA mismatch repair and TP53 defects are early events in uterine carcinosarcoma tumorigenesis.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2006;19(10):1333-8.
2006: Kabbarah Omar; Mallon Mary Ann; Pfeifer John D; Goodfellow Paul J
Transcriptional profiling endometrial carcinomas microdissected from DES-treated mice identifies changes in gene expression associated with estrogenic tumor promotion.
International journal of cancer. Journal international du cancer 2006;119(8):1843-9.
2006: Yu Jinsheng; Mallon Mary A; Zhang Wanghai; Freimuth Robert R; Marsh Sharon; Watson Mark A; Goodfellow Paul J; McLeod Howard L
DNA repair pathway profiling and microsatellite instability in colorectal cancer.
Clinical cancer research : an official journal of the American Association for Cancer Research 2006;12(17):5104-11.
2006: Taylor Nicholas P; Powell Matthew A; Gibb Randall K; Rader Janet S; Huettner Phyllis C; Thibodeau Stephen N; Mutch David G; Goodfellow Paul J
MLH3 mutation in endometrial cancer.
Cancer research 2006;66(15):7502-8.
2006: Taylor Nicholas P; Gibb Randall K; Powell Matthew A; Mutch David G; Huettner Phyllis C; Goodfellow Paul J
Defective DNA mismatch repair and XRCC2 mutation in uterine carcinosarcomas.
Gynecologic oncology 2006;100(1):107-10.
2005: Marsh Sharon; Mallon Mary Ann; Goodfellow Paul; McLeod Howard L
Concordance of pharmacogenetic markers in germline and colorectal tumor DNA.
Pharmacogenomics 2005;6(8):873-7.
2005: Read Renee D; Goodfellow Paul J; Mardis Elaine R; Novak Nancy; Armstrong Jon R; Cagan Ross L
A Drosophila model of multiple endocrine neoplasia type 2.
Genetics 2005;171(3):1057-81.
2005: Shin Brian Y; Chen Huiping; Rozek Laura S; Paxton Leslie; Peel David J; Anton-Culver Hoda; Rennert Gad; Mutch David G; Goodfellow Paul J; Gruber Stephen B; Lipkin Steve M
Low allele frequency of MLH1 D132H in American colorectal and endometrial cancer patients.
Diseases of the colon and rectum 2005;48(9):1723-7.
2005: Kabbarah Omar; Sotelo Andrea K; Mallon Mary Ann; Winkeler Erin L; Fan Ming-Yu; Pfeifer John D; Shibata Darryl; Gutmann David H; Goodfellow Paul J
Diethylstilbestrol effects and lymphomagenesis in Mlh1-deficient mice.
International journal of cancer. Journal international du cancer 2005;115(4):666-9.
2005: Skinner Michael A; Kalyanaraman Somasundaram; Safford Shawn D; Heuckeroth Robert O; Tourtellotte Warren; Goyeau Dominique; Goodfellow Paul; Milbrandt Jeffrey D; Freemerman Alex
A human yeast artificial chromosome containing the multiple endocrine neoplasia type 2B Ret mutation does not induce medullary thyroid carcinoma but does support the growth of kidneys and partially rescues enteric nervous system development in Ret-deficient mice.
The American journal of pathology 2005;166(1):265-74.
2005: Li Jianduan; Zhang Zhengyan; Bidder Miri; Funk Margo C; Nguyen Loan; Goodfellow Paul J; Rader Janet S
IGSF4 promoter methylation and expression silencing in human cervical cancer.
Gynecologic oncology 2005;96(1):150-8.
2004: Buttin Barbara M; Powell Matthew A; Mutch David G; Babb Sheri A; Huettner Phyllis C; Edmonston Tina Bocker; Herzog Thomas J; Rader Janet S; Gibb Randall K; Whelan Alison J; Goodfellow Paul J
Penetrance and expressivity of MSH6 germline mutations in seven kindreds not ascertained by family history.
American journal of human genetics 2004;74(6):1262-9.
2004: Kibel Adam S; Huagen John; Guo Chan; Isaacs William B; Yan Yan; Pienta Kenneth J; Goodfellow Paul J
Expression mapping at 12p12-13 in advanced prostate carcinoma.
International journal of cancer. Journal international du cancer 2004;109(5):668-72.
2004: Mutch David G; Powell Matthew A; Mallon Mary Ann; Goodfellow Paul J
RAS/RAF mutation and defective DNA mismatch repair in endometrial cancers.
American journal of obstetrics and gynecology 2004;190(4):935-42.
2004: Buttin Barbara M; Powell Matthew A; Mutch David G; Rader Janet S; Herzog Thomas J; Gibb Randall K; Huettner Phyllis; Edmonston Tina Bocker; Goodfellow Paul J
Increased risk for hereditary nonpolyposis colorectal cancer-associated synchronous and metachronous malignancies in patients with microsatellite instability-positive endometrial carcinoma lacking MLH1 promoter methylation.
Clinical cancer research : an official journal of the American Association for Cancer Research 2004;10(2):481-90.
2003: Kabbarah Omar; Mallon Mary Ann; Pfeifer John D; Edelmann Winfried; Kucherlapati Raju; Goodfellow Paul J
A panel of repeat markers for detection of microsatellite instability in murine tumors.
Molecular carcinogenesis 2003;38(4):155-9.
2003: Gutmann D H; Winkeler E; Kabbarah O; Hedrick N; Dudley S; Goodfellow P J; Liskay R M
Mlh1 deficiency accelerates myeloid leukemogenesis in neurofibromatosis 1 (Nf1) heterozygous mice.
Oncogene 2003;22(29):4581-5.
2003: Wilson David B; Ivanovich Jennifer; Whelan Alison; Goodfellow Paul J; Bessler Monica
Human telomerase RNA mutations and bone marrow failure.
Lancet 2003;361(9373):1993-4.
2003: Whitcomb Bradford P; Mutch David G; Herzog Thomas J; Rader Janet S; Gibb Randall K; Goodfellow Paul J
Frequent HOXA11 and THBS2 promoter methylation, and a methylator phenotype in endometrial adenocarcinoma.
Clinical cancer research : an official journal of the American Association for Cancer Research 2003;9(6):2277-87.
2003: Goodfellow Paul J; Buttin Barbara M; Herzog Thomas J; Rader Janet S; Gibb Randall K; Swisher Elizabeth; Look Katherine; Walls Ken C; Fan Ming-Yu; Mutch David G
Prevalence of defective DNA mismatch repair and MSH6 mutation in an unselected series of endometrial cancers.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(10):5908-13.
2003: Kibel Adam S; Suarez Brian K; Belani Jay; Oh Joe; Webster Raul; Brophy-Ebbers Michele; Guo Chan; Catalona William J; Picus Joel; Goodfellow Paul J
CDKN1A and CDKN1B polymorphisms and risk of advanced prostate carcinoma.
Cancer research 2003;63(9):2033-6.
2003: Kabbarah Omar; Pinto Karen; Mutch David G; Goodfellow Paul J
Expression profiling of mouse endometrial cancers microdissected from ethanol-fixed, paraffin-embedded tissues.
The American journal of pathology 2003;162(3):755-62.
2003: Noonan Ferrin C; Goodfellow Paul J; Staloch Lora J; Mutch David G; Simon Theodore C
Antisense transcripts at the EMX2 locus in human and mouse.
Genomics 2003;81(1):58-66.
2002: Horowitz N; Pinto K; Mutch D G; Herzog T J; Rader J S; Gibb R; Bocker-Edmonston T; Goodfellow P J
Microsatellite instability, MLH1 promoter methylation, and loss of mismatch repair in endometrial cancer and concomitant atypical hyperplasia.
Gynecologic oncology 2002;86(1):62-8.
2002: Whelan Alison J; Babb Sheri; Mutch David G; Rader Janet; Herzog Thomas J; Todd Christina; Ivanovich Jennifer L; Goodfellow Paul J
MSI in endometrial carcinoma: absence of MLH1 promoter methylation is associated with increased familial risk for cancers.
International journal of cancer. Journal international du cancer 2002;99(5):697-704.
2002: Powell Matthew A; Mutch David G; Rader Janet S; Herzog Thomas J; Huang Tim Hui-Ming; Goodfellow Paul J
Ribosomal DNA methylation in patients with endometrial carcinoma: an independent prognostic marker.
Cancer 2002;94(11):2941-52.
2002: Ivanovich Jennifer; Babb Sheri; Goodfellow Paul; Mutch David; Herzog Thomas; Rader Janet; Whelan Alison
Evaluation of the family history collection process and the accuracy of cancer reporting among a series of women with endometrial cancer.
Clinical cancer research : an official journal of the American Association for Cancer Research 2002;8(6):1849-56.
2001: Cohn D E; Mutch D G; Herzog T J; Rader J S; Dintzis S M; Gersell D J; Todd C R; Goodfellow P J
Genotypic and phenotypic progression in endometrial tumorigenesis: determining when defects in DNA mismatch repair and KRAS2 occur.
Genes, chromosomes & cancer 2001;32(4):295-301.
2001: Braybrook C; Doudney K; Marçano A C; Arnason A; Bjornsson A; Patton M A; Goodfellow P J; Moore G E; Stanier P
The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia.
Nature genetics 2001;29(2):179-83.
2001: Kibel A S; Christopher M; Faith D A; Bova G S; Goodfellow P J; Isaacs W B
Methylation and mutational analysis of p27(kip1) in prostate carcinoma.
The Prostate 2001;48(4):248-53.
2001: Noonan F C; Mutch D G; Ann Mallon M; Goodfellow P J
Characterization of the homeodomain gene EMX2: sequence conservation, expression analysis, and a search for mutations in endometrial cancers.
Genomics 2001;76(1-3):37-44.
2001: Cohn D; Mutch D; Elbendary A; Rader J; Herzog T; Goodfellow P
No evidence for BCL10 mutation in endometrial cancers with microsatellite instability.
Human mutation 2001;17(2):117-21.
2000: Basil J B; Goodfellow P J; Rader J S; Mutch D G; Herzog T J
Clinical significance of microsatellite instability in endometrial carcinoma.
Cancer 2000;89(8):1758-64.
2000: Cohn D E; Basil J B; Venegoni A R; Mutch D G; Rader J S; Herzog T J; Gersell D J; Goodfellow P J
Absence of PTEN repeat tract mutation in endometrial cancers with microsatellite instability.
Gynecologic oncology 2000;79(1):101-6.
2000: Mason J E; Goodfellow P J; Grundy P E; Skinner M A
16q loss of heterozygosity and microsatellite instability in Wilms' tumor.
Journal of pediatric surgery 2000;35(6):891-6; discussion 896-7.
2000: Cohn D E; Babb S; Whelan A J; Mutch D G; Herzog T J; Rader J S; Elbendary A; Goodfellow P J
Atypical clustering of gynecologic malignancies: A family study including molecular analysis of candidate genes.
Gynecologic oncology 2000;77(1):18-25.
1999: Basil J B; Swisher E M; Herzog T J; Rader J S; Elbendary A; Mutch D G; Goodfellow P J
Mutational analysis of the PMS2 gene in sporadic endometrial cancers with microsatellite instability.
Gynecologic oncology 1999;74(3):395-9.
1999: Arlt M F; Li M; Herzog T J; Goodfellow P J
A 1-Mb bacterial clone contig spanning the endometrial cancer deletion region at 1p32-p33.
Genomics 1999;57(1):62-9.
1999: Simpkins S B; Bocker T; Swisher E M; Mutch D G; Gersell D J; Kovatich A J; Palazzo J P; Fishel R; Goodfellow P J
MLH1 promoter methylation and gene silencing is the primary cause of microsatellite instability in sporadic endometrial cancers.
Human molecular genetics 1999;8(4):661-6.
1999: Herfarth K K; Brent T P; Danam R P; Remack J S; Kodner I J; Wells S A; Goodfellow P J
A specific CpG methylation pattern of the MGMT promoter region associated with reduced MGMT expression in primary colorectal cancers.
Molecular carcinogenesis 1999;24(2):90-8.
1999: Swisher E M; Peiffer-Schneider S; Mutch D G; Herzog T J; Rader J S; Elbendary A; Goodfellow P J
Differences in patterns of TP53 and KRAS2 mutations in a large series of endometrial carcinomas with or without microsatellite instability.
Cancer 1999;85(1):119-26.
1999: Mutch M G; Dilley W G; Sanjurjo F; DeBenedetti M K; Doherty G M; Wells S A; Goodfellow P J; Lairmore T C
Germline mutations in the multiple endocrine neoplasia type 1 gene: evidence for frequent splicing defects.
Human mutation 1999;13(3):175-85.
1998: Simpkins S B; Peiffer-Schneider S; Mutch D G; Gersell D; Goodfellow P J
PTEN mutations in endometrial cancers with 10q LOH: additional evidence for the involvement of multiple tumor suppressors.
Gynecologic oncology 1998;71(3):391-5.
1998: Peiffer-Schneider S; Noonan F C; Mutch D G; Simpkins S B; Herzog T; Rader J; Elbendary A; Gersell D J; Call K; Goodfellow P J
Mapping an endometrial cancer tumor suppressor gene at 10q25 and development of a bacterial clone contig for the consensus deletion interval.
Genomics 1998;52(1):9-16.
1998: Swisher E M; Mutch D G; Herzog T J; Rader J S; Kowalski L D; Elbendary A; Goodfellow P J
Analysis of MSH3 in endometrial cancers with defective DNA mismatch repair.
Journal of the Society for Gynecologic Investigation 1998;5(4):210-6.
1998: Ogunbiyi O A; Goodfellow P J; Herfarth K; Gagliardi G; Swanson P E; Birnbaum E H; Read T E; Fleshman J W; Kodner I J; Moley J F
Confirmation that chromosome 18q allelic loss in colon cancer is a prognostic indicator.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 1998;16(2):427-33.
1998: Klaus K; Herfarth F; Ogunbiyi O A; Moley J F; Kodner I J; Wells S A; Goodfellow P J
Four new mutations in the DNA mismatch repair gene MLH1 in colorectal cancers with microsatellite instability. Mutations in brief no. 157. Online.
Human mutation 1998;12(1):73.
1997: Ogunbiyi O A; Goodfellow P J; Gagliardi G; Swanson P E; Birnbaum E H; Fleshman J W; Kodner I J; Moley J F
Prognostic value of chromosome 1p allelic loss in colon cancer.
Gastroenterology 1997;113(3):761-6.
1997: Musholt P B; Musholt T J; Goodfellow P J; Zehnbauer B A; Wells S A; Moley J F
"Cold" single-strand conformational variants for mutation analysis of the RET protooncogene.
Surgery 1997;122(2):363-70; discussion 370-1.
1997: Kitamura Y; Goodfellow P J; Shimizu K; Nagahama M; Ito K; Kitagawa W; Akasu H; Takami H; Tanaka S; Wells S A
Novel germline RET proto-oncogene mutations associated with medullary thyroid carcinoma (MTC): mutation analysis in Japanese patients with MTC.
Oncogene 1997;14(25):3103-6.
1997: Tung W S; Shevlin D W; Kaleem Z; Tribune D J; Wells S A; Goodfellow P J
Allelotype of follicular thyroid carcinomas reveals genetic instability consistent with frequent nondisjunctional chromosomal loss.
Genes, chromosomes & cancer 1997;19(1):43-51.
1997: Musholt T J; Goodfellow P J; Scheumann G F; Pichlmayr R; Wells S A; Moley J F
Differential display in primary and metastatic medullary thyroid carcinoma.
The Journal of surgical research 1997;69(1):94-100.
1997: Kowalski L D; Mutch D G; Herzog T J; Rader J S; Goodfellow P J
Mutational analysis of MLH1 and MSH2 in 25 prospectively-acquired RER+ endometrial cancers.
Genes, chromosomes & cancer 1997;18(3):219-27.
1997: Elliott J L; Kwon J M; Goodfellow P J; Yee W C
Hereditary motor and sensory neuropathy IIB: clinical and electrodiagnostic characteristics.
Neurology 1997;48(1):23-8.
1997: Herfarth K K; Kodner I J; Whelan A J; Ivanovich J L; Bracamontes J R; Wells S A; Goodfellow P J
Mutations in MLH1 are more frequent than in MSH2 in sporadic colorectal cancers with microsatellite instability.
Genes, chromosomes & cancer 1997;18(1):42-9.
1996: Hammoud Z T; Kaleem Z; Cooper J D; Sundaresan R S; Patterson G A; Goodfellow P J
Allelotype analysis of esophageal adenocarcinomas: evidence for the involvement of sequences on the long arm of chromosome 4.
Cancer research 1996;56(19):4499-502.
1996: Arlt M F; Goodfellow P J; Rottman J N
Dinucleotide repeat in the third intron of the FABP3/MDGI putative tumor suppressor gene.
Disease markers 1996;13(1):57-9.
1996: Arlt M F; Herzog T J; Mutch D G; Gersell D J; Liu H; Goodfellow P J
Frequent deletion of chromosome 1p sequences in an aggressive histologic subtype of endometrial cancer.
Human molecular genetics 1996;5(7):1017-21.
1996: Bartsch D; Shevlin D W; Callery M P; Norton J A; Wells S A; Goodfellow P J
Reduced survival in patients with ductal pancreatic adenocarcinoma associated with CDKN2 mutation.
Journal of the National Cancer Institute 1996;88(10):680-2.
1996: Bartsch D; Peiffer S L; Kaleem Z; Wells S A; Goodfellow P J
Mxi1 tumor suppressor gene is not mutated in primary pancreatic adenocarcinoma.
Cancer letters 1996;102(1-2):73-6.
1996: Arlt M F; Herzog T J; Mutch D G; Goodfellow P J
Loss of heterozygosity of chromosome 3p sequences is an infrequent event in endometrial cancer.
Gynecologic oncology 1996;60(2):308-12.
1996: Tung W S; Shevlin D W; Bartsch D; Norton J A; Wells S A; Goodfellow P J
Infrequent CDKN2 mutation in human differentiated thyroid cancers.
Molecular carcinogenesis 1996;15(1):5-10.
1995: Bartsch D; Shevlin D W; Tung W S; Kisker O; Wells S A; Goodfellow P J
Frequent mutations of CDKN2 in primary pancreatic adenocarcinomas.
Genes, chromosomes & cancer 1995;14(3):189-95.
1995: Kitamura Y; Scavarda N; Wells S A; Jackson C E; Goodfellow P J
Two maternally derived missense mutations in the tyrosine kinase domain of the RET protooncogene in a patient with de novo MEN 2B.
Human molecular genetics 1995;4(10):1987-8.
1995: Whelan A J; Bartsch D; Goodfellow P J
Brief report: a familial syndrome of pancreatic cancer and melanoma with a mutation in the CDKN2 tumor-suppressor gene.
The New England journal of medicine 1995;333(15):975-7.
1995: Neuman R J; Kwon J M; Jilek-Aall L; Rwiza H T; Rice J P; Goodfellow P J
Genetic analysis of kifafa, a complex familial seizure disorder.
American journal of human genetics 1995;57(4):902-10.
1995: Kwon J M; Elliott J L; Yee W C; Ivanovich J; Scavarda N J; Moolsintong P J; Goodfellow P J
Assignment of a second Charcot-Marie-Tooth type II locus to chromosome 3q.
American journal of human genetics 1995;57(4):853-8.
1995: Goodfellow P J; Wells S A
RET gene and its implications for cancer.
Journal of the National Cancer Institute 1995;87(20):1515-23.
1995: Peiffer S L; Bartsch D; Whelan A J; Mutch D G; Herzog T J; Goodfellow P J
Low frequency of CDKN2 mutation in endometrial carcinomas.
Molecular carcinogenesis 1995;13(4):210-2.
1995: Stadler H S; Murray J C; Leysens N J; Goodfellow P J; Solursh M
Phylogenetic conservation and physical mapping of members of the H6 homeobox gene family.
Mammalian genome : official journal of the International Mammalian Genome Society 1995;6(6):383-8.
1995: Peiffer S L; Herzog T J; Tribune D J; Mutch D G; Gersell D J; Goodfellow P J
Allelic loss of sequences from the long arm of chromosome 10 and replication errors in endometrial cancers.
Cancer research 1995;55(9):1922-6.
1994: Carlson K M; Bracamontes J; Jackson C E; Clark R; Lacroix A; Wells S A; Goodfellow P J
Parent-of-origin effects in multiple endocrine neoplasia type 2B.
American journal of human genetics 1994;55(6):1076-82.
1994: Gorski S M; Adams K J; Birch P H; Chodirker B N; Greenberg C R; Goodfellow P J
Linkage analysis of X-linked cleft palate and ankyloglossia in Manitoba Mennonite and British Columbia Native kindreds.
Human genetics 1994;94(2):141-8.
1994: Goodfellow P J
Inherited cancers associated with the RET proto-oncogene.
Current opinion in genetics & development 1994;4(3):446-52.
1994: Goodfellow P J
Mapping the inherited defects associated with multiple endocrine neoplasia type 2A, multiple endocrine neoplasia type 2B, and familial medullary thyroid carcinoma to chromosome 10 by linkage analysis.
Endocrinology and metabolism clinics of North America 1994;23(1):177-85.
1994: Carlson K M; Dou S; Chi D; Scavarda N; Toshima K; Jackson C E; Wells S A; Goodfellow P J; Donis-Keller H
Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(4):1579-83.
1994: Billingsley G D; Cox D W; Duncan A M; Goodfellow P J; Grzeschik K H
Regional localization of loci on chromosome 14 using somatic cell hybrids.
Cytogenetics and cell genetics 1994;66(1):33-8.
1993: Horne C; Goodfellow P J; McDonald H L; Junker A K; Keown P A; Hoar D I
A new HLA-DRB1 allele formed by an intraexonic interallelic crossover.
Tissue antigens 1993;42(3):141-3.
1993: Brooks-Wilson A R; Lichter J B; Ward D C; Kidd K K; Goodfellow P J
Genomic and yeast artificial chromosome long-range physical maps linking six loci in 10q11.2 and spanning the multiple endocrine neoplasia type 2A (MEN2A) region.
Genomics 1993;17(3):611-7.
1993: Donis-Keller H; Dou S; Chi D; Carlson K M; Toshima K; Lairmore T C; Howe J R; Moley J F; Goodfellow P; Wells S A
Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC.
Human molecular genetics 1993;2(7):851-6.
1993: Lichter J B; Difilippantonio M J; Pakstis A J; Goodfellow P J; Ward D C; Kidd K K
Physical and genetic maps for chromosome 10.
Genomics 1993;16(2):320-4.
1993: Smith M J; Goodfellow P J; Goodfellow P N
The genomic organisation of the human pseudoautosomal gene MIC2 and the detection of a related locus.
Human molecular genetics 1993;2(4):417-22.
1993: Lichter J B; Wu J; Brooks-Wilson A R; Difillipantonio M; Brewster S; Ward D C; Goodfellow P J; Kidd K K
A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus.
Human genetics 1993;90(5):516-20.
1992: Ogata T; Petit C; Rappold G; Matsuo N; Matsumoto T; Goodfellow P
Chromosomal localisation of a pseudoautosomal growth gene(s).
Journal of medical genetics 1992;29(9):624-8.
1992: Narod S A; Lavoué M F; Morgan K; Calmettes C; Sobol H; Goodfellow P J; Lenoir G M
Genetic analysis of 24 French families with multiple endocrine neoplasia type 2A.
American journal of human genetics 1992;51(3):469-77.
1992: Lichter J B; Wu J; Miller D; Goodfellow P J; Kidd K K
A high-resolution meiotic mapping panel for the pericentromeric region of chromosome 10.
Genomics 1992;13(3):607-12.
1992: Miller D L; Dill F J; Lichter J B; Kidd K K; Goodfellow P J
Isolation and high-resolution mapping of new DNA markers from the pericentromeric region of chromosome 10.
Genomics 1992;13(3):601-6.
1992: Brooks-Wilson A R; Smailus D E; Weier H U; Goodfellow P J
Human repeat element-mediated PCR: cloning and mapping of chromosome 10 DNA markers.
Genomics 1992;13(2):409-14.
1992: McDonald H; Smailus D; Jenkins H; Adams K; Simpson N E; Goodfellow P J
Identification and characterization of a gene at D10S94 in the MEN2A region.
Genomics 1992;13(2):344-8.
1992: Brooks-Wilson A R; Smailus D E; Goodfellow P J
A cluster of CpG islands at D10S94, near the locus responsible for multiple endocrine neoplasia type 2A (MEN2A).
Genomics 1992;13(2):339-43.
1992: Gorski S M; Adams K J; Birch P H; Friedman J M; Goodfellow P J
The gene responsible for X-linked cleft palate (CPX) in a British Columbia native kindred is localized between PGK1 and DXYS1.
American journal of human genetics 1992;50(5):1129-36.
1992: Eccles M R; Wallis L J; Fidler A E; Spurr N K; Goodfellow P J; Reeve A E
Expression of the PAX2 gene in human fetal kidney and Wilms' tumor.
Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research 1992;3(5):279-89.
1992: Brooks-Wilson A R; Smailus D; Gilchrist D; Goodfellow P J
Additional RFLPs at D10S94 and the development of PCR-based variant detection systems: implications for disease genotype prediction in MEN 2A, MEN 2B, and MTC1 families.
Genomics 1992;13(1):233-4.
1992: Lamothe E M; Narod S A; Miller S; Goodfellow P J; Cole D E; Gilchrist D; Pausova Z; Goltzman D; Hendy G N
Screening for multiple endocrine neoplasia type 2A with DNA-polymorphism analysis.
Henry Ford Hospital medical journal 1992;40(3-4):224-6.
1992: Lichter J B; Hackleman S M; Ponder B A; Easton D; Narod S A; Lenoir G M; Gagel R F; Simpson N E; Gardner E; Goodfellow P J
A preliminary analysis of consortium data for markers tightly linked to multiple endocrine neoplasia type 2A.
Henry Ford Hospital medical journal 1992;40(3-4):205-9.
1992: Lichter J B; Difilippantonio M; Wu J; Miller D; Ward D C; Goodfellow P J; Kidd K K
Localization of the gene for MEN 2A.
Henry Ford Hospital medical journal 1992;40(3-4):199-204.
1991: Astrin K H; Warner C A; Yoo H W; Goodfellow P J; Tsai S F; Desnick R J
Regional assignment of the human uroporphyrinogen III synthase (UROS) gene to chromosome 10q25.2----q26.3.
Human genetics 1991;87(1):18-22.
1991: Weber B; Allen L; Magenis R E; Goodfellow P J; Smith L; Hayden M R
Intrachromosomal location of the telomeric repeat (TTAGGG)n.
Mammalian genome : official journal of the International Mammalian Genome Society 1991;1(4):211-6.
1990: Goodfellow P J; Myers S; Anderson L L; Brooks-Wilson A R; Simpson N E
A new DNA marker (D10S94) very tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus.
American journal of human genetics 1990;47(6):952-6.
1990: Miller D L; Smailus D; Goodfellow P J
An EcoRI RFLP at the D10S103 locus.
Nucleic acids research 1990;18(20):6177.
1990: Brooks-Wilson A R; Goodfellow P N; Povey S; Nevanlinna H A; de Jong P J; Goodfellow P J
Rapid cloning and characterization of new chromosome 10 DNA markers by Alu element-mediated PCR.
Genomics 1990;7(4):614-20.
1990: Goodfellow P J; Brooks-Wilson A R; Smailus D; Myers S; Anderson L; Simpson N E
Three polymorphisms at the D10S85 locus.
Nucleic acids research 1990;18(16):4960.
1990: Brooks-Wilson A R; Smailus D; Myers S; Anderson L; Simpson N E; Goodfellow P J
Two polymorphisms at the D10S94 locus.
Nucleic acids research 1990;18(16):4959.
1990: Ellis N; Kidd J; Goodfellow P J; Kidd K; Goodfellow P N
Strong linkage disequilibrium between the XY274 polymorphism and the pseudoautosomal boundary.
American journal of human genetics 1990;46(5):950-5.
1990: Goodfellow P J; Povey S; Nevanlinna H A; Goodfellow P N
Generation of a panel of somatic cell hybrids containing unselected fragments of human chromosome 10 by X-ray irradiation and cell fusion: application to isolating the MEN2A region in hybrid cells.
Somatic cell and molecular genetics 1990;16(2):163-71.
1989: Wu J S; Giuffra L A; Goodfellow P J; Myers S; Carson N L; Anderson L; Hoyle L S; Simpson N E; Kidd K K
The beta subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies.
Human genetics 1989;83(4):383-90.
1989: Beverstock G C; MacFarlane J D; Veenema H; Hoekman H; Goodfellow P J
Y chromosome specific probes identify breakpoint in a 45,X/46,X,del(Y)(pter----q11.1:) karyotype of an infertile male.
Journal of medical genetics 1989;26(5):330-3.
1989: Ellis N A; Goodfellow P J; Pym B; Smith M; Palmer M; Frischauf A M; Goodfellow P N
The pseudoautosomal boundary in man is defined by an Alu repeat sequence inserted on the Y chromosome.
Nature 1989;337(6202):81-4.
1989: Goodfellow P J; Nevanlinna H A; Gorman P; Sheer D; Lam G; Goodfellow P N
Assignment of the gene encoding the beta-subunit of the human fibronectin receptor (beta-FNR) to chromosome 10p11.2.
Annals of human genetics 1989;53(Pt 1):15-22.
1988: Goodfellow P N; Pym B; Pritchard C; Ellis N; Palmer M; Smith M; Goodfellow P J
MIC2: a human pseudoautosomal gene.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences 1988;322(1208):145-54.
1988: Goodfellow P J; Mondello C; Darling S M; Pym B; Little P; Goodfellow P N
Absence of methylation of a CpG-rich region at the 5' end of the MIC2 gene on the active X, the inactive X, and the Y chromosome.
Proceedings of the National Academy of Sciences of the United States of America 1988;85(15):5605-9.
1988: Mondello C; Goodfellow P J; Goodfellow P N
Analysis of methylation of a human X located gene which escapes X inactivation.
Nucleic acids research 1988;16(14B):6813-24.
1988: Spurr N K; Gough A; Goodfellow P J; Goodfellow P N; Lee M G; Nurse P
Evolutionary conservation of the human homologue of the yeast cell cycle control gene cdc2 and assignment of Cd2 to chromosome 10.
Human genetics 1988;78(4):333-7.
1987: Goodfellow P J; Goodfellow P N; Spurr N K
A BamHI RFLP recognised by an anonymous chromosome 20 probe, p4.8 (D20S14).
Nucleic acids research 1987;15(17):7213.
1987: Pritchard C A; Goodfellow P J; Goodfellow P N
Isolation of a sequence which maps close to the human sex determining gene.
Nucleic acids research 1987;15(15):6159-69.
1987: Simpson N E; Kidd K K; Goodfellow P J; McDermid H; Myers S; Kidd J R; Jackson C E; Duncan A M; Farrer L A; Brasch K
Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage.
Nature 1987;328(6130):528-30.
1987: Farrer L A; Goodfellow P J; White B N; Holden J J; Kidd J R; Simpson N E; Kidd K K
Linkage analysis of multiple endocrine neoplasia type 2A (MEN-2A) and three DNA markers on chromosome 20: evidence against synteny.
Cancer genetics and cytogenetics 1987;27(2):327-34.
1987: McDermid H E; Goodfellow P J; Duncan A M; Brasch K R; Simpson N E; Souza C D; Holden J J; White B N
A polymorphic locus, D10S5, at 10q21.1.
Nucleic acids research 1987;15(13):5498.
1987: Pritchard C A; Goodfellow P J; Goodfellow P N
Mapping the limits of the human pseudoautosomal region and a candidate sequence for the male-determining gene.
Nature 1987;328(6127):273-5.
1987: Goodfellow P J; Pritchard C; Tippett P; Goodfellow P N
Recombination between the X and Y chromosomes: implications for the relationship between MIC2, XG and YG.
Annals of human genetics 1987;51(Pt 2):161-7.
1987: Buckle V J; Boyd Y; Fraser N; Goodfellow P N; Goodfellow P J; Wolfe J; Craig I W
Localisation of Y chromosome sequences in normal and 'XX' males.
Journal of medical genetics 1987;24(4):197-203.
1987: Farrer L A; Goodfellow P J; Lamarche C M; Franjkovic I; Myers S; White B N; Holden J J; Kidd J R; Simpson N E; Kidd K K
An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13.
American journal of human genetics 1987;40(4):329-37.
1987: Goodfellow P J; Darling S; Banting G; Pym B; Mondello C; Goodfellow P N
Pseudoautosomal genes in man.
Development (Cambridge, England) 1987;101 Suppl():119-25.
1987: Goodfellow P J; Duncan A M; Farrer L A; Holden J J; White B N; Kidd J R; Kidd K K; Simpson N E
Localization and linkage of three polymorphic DNA sequences on human chromosome 20.
Cytogenetics and cell genetics 1987;44(2-3):112-7.
1986: Goodfellow P J; Duncan A M; Simpson N E; White B N
pG95 alpha 1-7dIII/RI, a single copy clone at Xp11.4 which recognises a TaqI polymorphism (DXS209).
Nucleic acids research 1986;14(21):8693.
1986: Goodfellow P J; Darling S M; Thomas N S; Goodfellow P N
A pseudoautosomal gene in man.
Science (New York, N.Y.) 1986;234(4777):740-3.
1986: Goodfellow P J; Duncan A M; Simpson N E; White B N
Three RFLPs recognized by an anonymous sequence localized to 21q11.2 [HGM8 D21S72]
Nucleic acids research 1986;14(10):4375.
1986: Darling S M; Goodfellow P J; Pym B; Banting G S; Pritchard C; Goodfellow P N
Molecular genetics of MIC2: a gene shared by the human X and Y chromosomes.
Cold Spring Harbor symposia on quantitative biology 1986;51 Pt 1():205-12.
1985: Goodfellow P J; White B N; Holden J J; Duncan A M; Sears E V; Wang H S; Berlin L; Kidd K K; Simpson N E
Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A.
American journal of human genetics 1985;37(5):890-7.

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