W. Noll

发表

The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis.

C Eng, P Komminoth, D. Clayton, 1996, JAMA.

Loss of heterozygosity on chromosome 11q22-23 in melanoma is associated with retention of the insertion polymorphism in the matrix metalloproteinase-1 promoter.

A. Schned, M. Ernstoff, J. Rutter, 2001, The American journal of pathology.

Paternally derived de novo interstitial duplication of proximal 15q in a patient with developmental delay.

T. Mohandas, A. Mamourian, J. Moeschler, 1999, American journal of medical genetics.

Multiple endocrine neoplasia 2A due to a unique C609S RET mutation presents with pheochromocytoma and reduced penetrance of medullary thyroid carcinoma

Robert D. Harris, G. Daniels, E. Spooner, 2005, Clinical endocrinology.

Factors Affecting the Detection Rate of Human Papillomavirus

D. Harper, M. Longacre, B. Cole, 2003, The Annals of Family Medicine.

V. Weedn, W. Grody, Marc Sobel, 2009, Archives of pathology & laboratory medicine.

Prognostic value of lymphocyte surface markers in acute myeloid leukemia.

J. Griffin, R. Mayer, D. Arthur, 1991, Blood.

Randomized clinical trial of PCR-determined human papillomavirus detection methods: self-sampling versus clinician-directed--biologic concordance and women's preferences.

D. Harper, B. Cole, D. Belloni, 2002, American journal of obstetrics and gynecology.

ited in an autosomal dominant pattern with a high degree of penetrance

W. Noll, J. Devlin, D. Wurster-Hill, 2006 .

Maternal disomy and Prader-Willi syndrome consistent with gamete complementation in a case of familial translocation (3;15) (p25;q11.2).

T. Mohandas, J. Moeschler, D. Belloni, 1998, American journal of medical genetics.

Rapid identification of overlapping YACs in the MEN2 region of human chromosome 10 by hybridization with Alu element-mediated PCR products.

D. Housman, D. Bowden, V. Stanton, 1993, Gene.

Transplantation of azaserine-induced carcinomas of pancreas in rats.

D. Longnecker, W. Noll, H. Lilja, 1979, Cancer letters.

Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results

W. Grody, D. Belloni, W. Noll, 1999, Nature Genetics.

Multicenter evaluation of PCR methods for the detection of factor V Leiden (R506Q) genotypes.

C. Lutz, K. Voelkerding, N. Kirschbaum, 1998, Clinical chemistry.

Detection of human DNA polymorphisms with a simplified denaturing gradient gel electrophoresis technique.

W. Noll, M. Collins, 1987, Proceedings of the National Academy of Sciences of the United States of America.

Genotype‐phenotype correlation in multiple endocrine neoplasia type 2: report of the International RET Mutation Consortium

B. Ponder, S. Thibodeau, L. Mulligan, 1995, Journal of internal medicine.

Rapid, nonradioactive screening for mutations in exons 10, 11, and 16 of the RET protooncogene associated with inherited medullary thyroid carcinoma.

S. Thibodeau, G. Tomlinson, D. Dawson, 1997, Clinical chemistry.

Identification of a second human acetyl-CoA carboxylase gene.

K. Kim, L. Witters, B. Crute, 1996, The Biochemical journal.

Localization of acyl coenzyme A:cholesterol acyltransferase gene to human chromosome 1q25

W. Chang, A. Baldini, Catherine C. Y. Chang, 1994, Somatic cell and molecular genetics.

Utility of RET mutation analysis in multiple endocrine neoplasia type 2.

W. Noll, 1999, Archives of pathology & laboratory medicine.

Isolation and growth characteristics of continuous cell lines from small‐cell carcinoma of the lung

G. Sorenson, W. Noll, L. H. Maurer, 1980, Cancer.

BRCA1 and BRCA2 mutations in women of different ethnicities undergoing testing for hereditary breast‐ovarian cancer

B. Ward, D. Pruss, J. Reid, 2009, Cancer.

Estimate of prevalence of proximal 15q duplication syndrome.

T. Mohandas, J. Moeschler, W. Noll, 2002, American journal of medical genetics.

Hypodiploid, pseudodiploid, and normal karyotypes prevail in cytogenetic studies of medullary carcinomas of the thyroid and metastatic tissues.

S. H. Gibson, W. Noll, T. Brinck-Johnsen, 1990, Cancer genetics and cytogenetics.

Cytogenetics of medullary carcinoma of the thyroid.

W. Noll, O. Pettengill, D. Wurster-Hill, 1986, Cancer genetics and cytogenetics.

Fragile sites and high-resolution chromosome studies in multiple endocrine neoplasia type 2A.

S. H. Gibson, R. Erbe, W. Noll, 1988, Cancer genetics and cytogenetics.

Kearns-Sayre syndrome with features of Pearson's marrow-pancreas syndrome and a novel 2905-base pair mitochondrial DNA deletion.

D. Price, O. Hurko, W. Noll, 1999, Human pathology.

Human Acyl-CoA:Cholesterol Acyltransferase-1 (ACAT-1) Gene Organization and Evidence That the 4.3-Kilobase ACAT-1 mRNA Is Produced from Two Different Chromosomes*

Zhi-Jun Duan, T. Mohandas, Zhi-jun Duan, 1999, The Journal of Biological Chemistry.

A genetic linkage map of 32 loci on human chromosome 10.

P. Green, D. Bowden, K. Falls, 1989, Genomics.

Some properties of mouse mastocytoma histidine decarboxylase

W. Noll, 1965 .

Diversity of cystic fibrosis mutation-screening practices.

W. Grody, R. Desnick, N. Carpenter, 1998, American journal of human genetics.

Constitutional de novo t(1;22)(p22;q11.2) and ependymoma.

W. Noll, S. Chaffee, J. P. Park, 1996, Cancer genetics and cytogenetics.

Amplification of the MLL region in acute myeloid leukemia.

T. Mohandas, W. Noll, J. P. Park, 2000, Cancer genetics and cytogenetics.

A novel method for creating artificial mutant samples for performance evaluation and quality control in clinical molecular genetics.

W. Grody, R. Iyer, L. Williams, 2005, The Journal of molecular diagnostics : JMD.

Characterization of radiation/fusion hybrids containing parts of human chromosome 10 and their use in mapping chromosome 10-specific probes.

D. Bowden, T. Gravius, C. Jones, 1992, Genomics.

The relationship of APOE genotype to neuropsychological performance in long‐term cancer survivors treated with standard dose chemotherapy

A. Saykin, T. Ahles, S. Guerin, 2003, Psycho-oncology.

Studies on the prevalence of type C virus associated with gibbon hematopoietic neoplasms.

P. Buckley, W. Noll, A. Depaoli, 1975, Bibliotheca haematologica.

Tampon Samplings With Longer Cervicovaginal Cell Exposures Are Equivalent to Two Consecutive Swabs for the Detection of High-Risk Human Papillomavirus

D. Harper, B. Cole, Meghan Raymond, 2002, Sexually transmitted diseases.

Germline RET mutations in MEN 2A and FMTC and their detection by simple DNA diagnostic tests.

D. Bowden, F. Xue, W. Noll, 1994, Human molecular genetics.

Histidine decarboxylase in gastric tissues of primates

R. Levine, W. Noll, 1970 .

HISTIDINE DECARBOXYLASE AND ITS INHIBITION

R. Levine, W. Noll, 1969, Annals of the New York Academy of Sciences.

A cytogenetic study of familial medullary carcinoma of the thyroid.

W. Noll, J. Devlin, D. Wurster-Hill, 1986, Cancer research.

Linkage Disequilibrium Analysis in a Recently Founded Population : Evaluation of the Variegate Porphyria Founder in South African Afrikaners

W. Grody, R. Desnick, N. Carpenter, 2007 .

The potential for increased clinical sensitivity in genetic testing for polyposis colorectal cancer through the analysis of MYH mutations in North American patients

E. Lyon, B. Ward, T. Scholl, 2005, Journal of Medical Genetics.