MaryPat Jones

发表

Genome‐wide scan of Swedish families with hereditary prostate cancer: Suggestive evidence of linkage at 5q11.2 and 19p13.3

E. Gillanders, H. Grönberg, F. Wiklund, 2003, The Prostate.

A Hereditary Form of Small Intestinal Carcinoid Associated With a Germline Mutation in Inositol Polyphosphate Multikinase.

R. Agarwala, A. Schäffer, S. Szymczak, 2015, Gastroenterology.

Guided genetic screen to identify genes essential in the regeneration of hair cells and other tissues

Shuo Lin, Haigen Huang, S. Burgess, 2018, npj Regenerative Medicine.

Combined genome-wide scan for prostate cancer susceptibility genes.

J. Carpten, E. Gillanders, J. Trent, 2004, Journal of the National Cancer Institute.

A high-throughput functional genomics workflow based on CRISPR/Cas9-mediated targeted mutagenesis in zebrafish

S. Burgess, Lisha Xu, Zelin Chen, 2016, Nature Protocols.

Genome-wide scanning for linkage in Finnish breast cancer families

E. Gillanders, J. Trent, O. Kallioniemi, 2004, European Journal of Human Genetics.

Multiplexed CRISPR/Cas9-mediated knockout of 19 Fanconi anemia pathway genes in zebrafish revealed their roles in growth, sexual development and fertility

R. Sood, S. Chandrasekharappa, D. Kimble, 2018, PLoS genetics.

The vitamin B12 processing enzyme, mmachc, is essential for zebrafish survival, growth and retinal morphology.

A. Elkahloun, V. Hoffmann, C. Venditti, 2020, Human molecular genetics.

CBFβ and RUNX1 are required at 2 different steps during the development of hematopoietic stem cells in zebrafish.

A. Gore, R. Sood, B. Weinstein, 2014, Blood.

development of hematopoietic stem cells in zebrafish and RUNX1 are required at 2 different steps during the β CBF

A. Gore, R. Sood, S. Wincovitch, 2014 .

CBF β and RUNX 1 are required at two different steps during the development of hematopoietic stem cells in zebrafish Short title for the running head : Distinct roles of CBF β and RUNX 1 in HSC production

A. Gore, R. Sood, B. Weinstein, 2014 .

HEMATOPOIESIS AND STEM CELLS CBF b and RUNX 1 are required at 2 different steps during the development of hematopoietic stem cells in zebra fi sh

A. Gore, R. Sood, B. Weinstein, 2014 .

Comparison of mutation findings in ZIC2 between microform and classical holoprosencephaly in a Brazilian cohort.

D. Pineda-Alvarez, A. Richieri‐Costa, M. Muenke, 2012, Birth defects research. Part A, Clinical and molecular teratology.

Methods for reverse genetic screening in zebrafish by resequencing and TILLING.

J. Mullikin, Jinghui Zhang, Dongying Wu, 2006, Methods.

Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3p.

Nancy F. Hansen, J. Mullikin, N. Hansen, 2010, Blood.

Brain-derived neurotrophic factor and obesity in the WAGR syndrome.

G. Uhl, Qing-Rong Liu, O. Rennert, 2008, The New England journal of medicine.

High-throughput gene targeting and phenotyping in zebrafish using CRISPR/Cas9

Kevin Bishop, Lisha Xu, Anupam Prakash, 2015, Genome research.

Genome‐wide scan for prostate cancer susceptibility genes in the Johns Hopkins hereditary prostate cancer families

E. Gillanders, J. Trent, Jianfeng Xu, 2003, The Prostate.

GWAS reveals new recessive loci associated with non-syndromic facial clefting.

B. Solomon, S. Chandrasekharappa, U. Harper, 2012, European journal of medical genetics.

Genetic heterogeneity in Finnish hereditary prostate cancer using ordered subset analysis

J. Schleutker, Tiina Wahlfors, T. Tammela, 2012, European Journal of Human Genetics.

Localization of a novel melanoma susceptibility locus to 1p22.

E. Gillanders, J. Trent, G. Mann, 2003, American journal of human genetics.

Efficient Methods for Targeted Mutagenesis in Zebrafish Using Zinc-Finger Nucleases: Data from Targeting of Nine Genes Using CompoZr or CoDA ZFNs

Kevin Bishop, Blake Carrington, R. Sood, 2013, PloS one.

Genome‐wide linkage scan for prostate cancer susceptibility in Finland: Evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21‐q22

Claire L. Simpson, J. Schleutker, Tiina Wahlfors, 2011, International journal of cancer.

Review of disrupted sleep patterns in Smith–Magenis syndrome and normal melatonin secretion in a patient with an atypical interstitial 17p11.2 deletion

M. Huizing, A. Lewy, E. Boudreau, 2009, American journal of medical genetics. Part A.

Genome-wide scanning for linkage in Finnish breast cancer families

E. Gillanders, J. Trent, O. Kallioniemi, 2004, European Journal of Human Genetics.

Reticular dysgenesis–associated AK2 protects hematopoietic stem and progenitor cell development from oxidative stress

A. Schambach, L. Notarangelo, W. Al-Herz, 2015, The Journal of experimental medicine.

Genome‐wide scan for prostate cancer susceptibility genes using families from the University of Michigan prostate cancer genetics project finds evidence for linkage on chromosome 17 near BRCA1

E. Gillanders, J. Trent, K. Cooney, 2003, The Prostate.

A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment

Tanya M. Teslovich, E. Gillanders, D. Stephan, 2006, European Journal of Human Genetics.

Hereditary prostate cancer in Finland: fine-mapping validates 3p26 as a major predisposition locus

E. Gillanders, J. Trent, Kenneth D. Gibbs, 2004, Human Genetics.

Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13

Tanya M. Teslovich, E. Gillanders, D. Stephan, 2003, Human Genetics.

Recombination mapping using Boolean logic and high-density SNP genotyping for exome sequence filtering.

D. Adams, C. Boerkoel, W. Gahl, 2012, Molecular genetics and metabolism.