M. E. Ahearn

发表

Interchromosomal segmental duplications explain the unusual structure of PRSS3, the gene for an inhibitor-resistant trypsinogen.

A. Kaur, L. Hood, B. Trask, 2005, Molecular biology and evolution.

TITLE: Defining Genomic Changes in Triple Negative Breast Cancer in Women of African Descent

M. Jordá, Carmen R Gomez, M. E. Ahearn, 2010 .

Analysis of the gene-dense major histocompatibility complex class III region and its comparison to mouse.

L. Hood, S. Qin, L. Rowen, 2003, Genome research.

Recurrent Third-Trimester Fetal Loss and Maternal Mosaicism for Long-QT Syndrome

R. Myerburg, N. Bishopric, G. Wolff, 2004, Circulation.

Genetic screening of cardiac syndromes

N. Bishopric, M. E. Ahearn, H. Elsayed, 2012 .

Structural rearrangements of the chloroplast genome provide an important phylogenetic link in ferns.

M. Hasebe, J. Thomson, S. Kirch, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Abstract 2368: Differential gene expression in key oncolytic pathways between node-matched Caucasian-American, African-American and East African triple-negative breast cancer patients

J. Carpten, J. Getz, M. Pegram, 2014 .

Review of X‐linked syndromes with arthrogryposis or early contractures—aid to diagnosis and pathway identification

Lisa Baumbach-Reardon, C. Balak, M. E. Ahearn, 2015, American journal of medical genetics. Part A.

A new species of Neochoerus (Rodentia: Hydrochoeridae) from the Blancan (Late Pliocene) of North America

M. E. Ahearn, J. F. Lance, 1980 .

Novel pathogenic variants and genes for myopathies identified by whole exome sequencing

Winnie S. Liang, J. Carpten, S. Coons, 2015, Molecular genetics & genomic medicine.

Functional characterizations of rare UBA1 variants in X-linked Spinal Muscular Atrophy

Lisa Baumbach-Reardon, D. Wiley, J. Hunter, 2017, F1000Research.

Spinal Muscular Atrophy, X-Linked Infantile

Lisa Baumbach-Reardon, M. E. Ahearn, S. Sacharow, 2012 .

Rare missense and synonymous variants in UBE1 are associated with X-linked infantile spinal muscular atrophy.

E. Hoffman, J. Ramser, A. Meindl, 2008, American journal of human genetics.

Phylogenetic implications of chloroplast DNA variation in the Cyatheaceae. I

P. Sudarsanam, D. Conant, D. B. Stein, 1991 .

X-linked infantile spinal muscular atrophy: Clinical definition and molecular mapping

D. Dressman, E. Hoffman, M. Barmada, 2007, Genetics in Medicine.

Dysfunctional potassium channel subunit interaction as a novel mechanism of long QT syndrome.

R. Myerburg, N. Bishopric, A. Farooq, 2013, Heart rhythm.

Dysfunctional potassium channel subunit interaction as a novel mechanism of long QT syndrome.

R. Myerburg, N. Bishopric, A. Farooq, 2013, Heart Rhythm.

Abstract A74: Differential Wnt signaling in African American and Caucasian women with triple-negative breast cancer

J. Carpten, J. Getz, M. Jordá, 2015 .