J. Stevens

发表

Siah-1 mediates a novel beta-catenin degradation pathway linking p53 to the adenomatous polyposis coli protein.

Raymond L. White, Jun Liu, R. White, 2001, Molecular cell.

The neurofibromatosis type 1 gene encodes a protein related to GAP

Margaret Robertson, Jeff Stevens, Peter O'Connell, 1990, Cell.

Genomic organization of the neurofibromatosis 1 gene (NF1).

P. O'Connell, R. Cawthon, Y. Li, 1995, Genomics.

A physical map and candidate genes in the BRCA1 region on chromosome 17q12–21

E. Fujimoto, B. Ponder, M. Robertson, 1994, Nature Genetics.

A role for the MEGF6 gene in predisposition to osteoporosis

L. Cannon-Albright, C. Teerlink, J. Facelli, 2020, bioRxiv.

Neuropathy target esterase gene mutations cause motor neuron disease.

H. Coon, M. Leppert, J. Albers, 2008, American journal of human genetics.

Absence of TGFBR1 and TGFBR2 mutations in patients with bicuspid aortic valve and aortic dilation.

M. Leppert, J. Stevens, N. Bowles, 2008, The American journal of cardiology.

A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations

P. O'Connell, M. Culver, R. Cawthon, 1990, Cell.

Two NF1 translocations map within a 600-kilobase segment of 17q11.2.

D. Ledbetter, P. O'Connell, M. Culver, 1989, Science.

Indian hedgehog signaling pathway differences between swarm rat chondrosarcoma and native rat chondrocytes.

J. Morcuende, J. Stevens, Pablo F Gomez, 2007, The Iowa orthopaedic journal.

Identification and initial characterization of 6,000 expressed sequenced tags (ESTs) from rat normal-growing cartilage and swarm rat chondrosarcoma cDNA libraries.

T. Casavant, T. Scheetz, J. Morcuende, 2002, The Iowa orthopaedic journal.

Evidence for Linkage on Chromosome 3q25–27 in a Large Autism Extended Pedigree

W. McMahon, H. Coon, Judith S Miller, 2006, Human Heredity.

Characterization of human adenylate kinase 3 (AK3) cDNA and mapping of the AK3 pseudogene to an intron of the NF1 gene.

P. O'Connell, R. White, J. Stevens, 1992, Genomics.

The human homolog of murine Evi-2 lies between two von Recklinghausen neurofibromatosis translocations.

D. Ledbetter, P. O'Connell, M. Culver, 1990, Genomics.

Sequence, genomic structure, and chromosomal assignment of human DOC-2.

R. White, J. Stevens, H. Albertsen, 1996, Genomics.

CRISPR/Cas9 mediated generation of stable chondrocyte cell lines with targeted gene knockouts; analysis of an aggrecan knockout cell line.

J. Stevens, G. Gibson, Maozhou Yang, 2014, Bone.

Somatic mutations in the neurofibromatosis 1 gene in human tumors

R. Cawthon, Y. Li, E. Friedman, 1992, Cell.

Identification and characterization of transcripts from the neurofibromatosis 1 region: the sequence and genomic structure of EVI2 and mapping of other transcripts.

P. O'Connell, M. Culver, R. Cawthon, 1990, Genomics.

Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2014, Molecular Autism.

Identification of Rare Recurrent Copy Number Variants in High-Risk Autism Families and Their Prevalence in a Large ASD Population

H. Hakonarson, Cecilia Kim, D. Hadley, 2013, PloS one.

Identification and characterization of the familial adenomatous polyposis coli gene

Margaret Robertson, Jeff Stevens, Joanna Groden, 1991, Cell.

Demonstration of Protein-Based Human Identification Using the Hair Shaft Proteome

David M. Rocke, Mark Leppert, Lisa Baird, 2016, PloS one.

A Rare Variant in ERF (rs144812092) Predisposes to Prostate and Bladder Cancers in an Extended Pedigree

J. Schleutker, L. Cannon-Albright, N. Agarwal, 2021, Cancers.

Germline but not somatic de novo mutations are common in human congenital diaphragmatic hernia.

M. Leppert, B. Yoder, J. Stevens, 2018, Birth defects research.

A high-density SNP genome-wide linkage scan in a large autism extended pedigree

J Miller, K Allen-Brady, M. Leppert, 2009, Molecular Psychiatry.

An intronic variant in the CELF4 gene is associated with risk for colorectal cancer.

L. Cannon-Albright, C. Teerlink, J. Facelli, 2021, Cancer epidemiology.

A Nonsynonymous Variant in the GOLM1 Gene in Cutaneous Malignant Melanoma

L. Cannon-Albright, J. Farnham, Alun Thomas, 2018, Journal of the National Cancer Institute.

Identification of deletion mutations and three new genes at the familial polyposis locus

J. McPherson, D. Paslier, J. Warrington, 1991, Cell.

Targeted degradation of β-catenin by chimeric F-box fusion proteins

R. White, J. Stevens, N. Matsunami, 2004 .

The gene encoding the oligodendrocyte-myelin glycoprotein is embedded within the neurofibromatosis type 1 gene

P. O'Connell, M. Culver, R. Cawthon, 1991, Molecular and cellular biology.

A likely HOXC4 predisposition variant for Chiari malformations.

L. Cannon-Albright, J. Heiss, J. Facelli, 2022, Journal of neurosurgery.

American founder mutation for attenuated familial adenomatous polyposis.

M. Leppert, J. Stevens, N. Matsunami, 2008, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

A hyperactivating proinflammatory RIPK2 allele associated with early-onset osteoarthritis

M. Leppert, J. Stevens, M. Jurynec, 2018, Human molecular genetics.

RIPK 2 allele associated with early-onset osteoarthritis

J. Stevens, M. Jurynec, D. Grunwald, 2018 .

Population‐wide Infant Screening for HLA‐Based Type 1 Diabetes Risk via Dried Blood Spots from the Public Health Infrastructure

Jeff Stevens, William Hagopian, W. Hagopian, 2003, Annals of the New York Academy of Sciences.

Isolation and mapping of a gene encoding a novel human ADP-ribosylation factor on chromosome 17q12-q21.

R. White, J. Stevens, H. Albertsen, 1995, Genomics.

High-Risk Pedigree Study Identifies LRBA (rs62346982) as a Likely Predisposition Variant for Prostate Cancer

L. Cannon-Albright, N. Agarwal, C. Teerlink, 2023, Cancers.

A rare FGF5 candidate variant (rs112475347) for predisposition to nonsquamous, nonsmall‐cell lung cancer

L. Cannon-Albright, C. Teerlink, J. Facelli, 2023, International journal of cancer.

A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations.

P. O'Connell, M. Culver, R. Cawthon, 1990, Cell.

Colorectal adenomas and cancer link to chromosome 13q22.1–13q31.3 in a large family with excess colorectal cancer

M. Leppert, W. Samowitz, J. Stevens, 2010, Journal of Medical Genetics.

Isolation of a gene (DLG3) encoding a second member of the discs-large family on chromosome 17q12-q21.

R. White, S. Mazoyer, J. Stevens, 1996, Genomics.

Targeted degradation of beta-catenin by chimeric F-box fusion proteins.

Raymond L. White, J. Stevens, N. Matsunami, 2004, Biochemical and biophysical research communications.

Demonstration of Protein-Based Human Identification Using the Hair Shaft Proteome

David M. Rocke, M. Leppert, S. Woodward, 2016, PloS one.

Corrigendum: A hyperactivating proinflammatory RIPK2 allele associated with early-onset osteoarthritis [Human Molecular Genetics, 27, 13, (2018), (2383-2391)] DOI: 10.1093/hmg/ddy132

M. Leppert, J. Stevens, M. Jurynec, 2018 .

A hyperactivating proinflammatory RIPK2 allele associated with early-onset osteoarthritis.

M. Leppert, J. Stevens, M. Jurynec, 2018, Human molecular genetics.

The University of Bradford Institutional Repository

David M. Rocke, M. Leppert, S. Woodward, 2022 .

Colorectal adenomas and cancer link to chromosome 13q22.1-13q31.3 in a large family with excess colorectal cancer

M. Leppert, W. Samowitz, J. Stevens, 2010, Journal of Medical Genetics.