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Patricia A.Ward
Patricia A.Ward
Verified email at bcm.edu
Title
Cited by
Cited by
Year
Clinical whole-exome sequencing for the diagnosis of mendelian disorders
Y Yang, DM Muzny, JG Reid, MN Bainbridge, A Willis, PA Ward, ...
New England Journal of Medicine 369 (16), 1502-1511, 2013
22032013
Molecular findings among patients referred for clinical whole-exome sequencing
Y Yang, DM Muzny, F Xia, Z Niu, R Person, Y Ding, P Ward, A Braxton, ...
Jama 312 (18), 1870-1879, 2014
14502014
Length of uninterrupted CGG repeats determines instability in the FMR1 gene
EE Eichler, JJA Holden, BW Popovich, AL Reiss, K Snow, SN Thibodeau, ...
Nature genetics 8 (1), 88-94, 1994
6101994
Use of exome sequencing for infants in intensive care units: ascertainment of severe single-gene disorders and effect on medical management
L Meng, M Pammi, A Saronwala, P Magoulas, AR Ghazi, F Vetrini, ...
JAMA pediatrics 171 (12), e173438-e173438, 2017
4112017
Percutaneous coronary intervention and adjunctive pharmacotherapy in women: a statement for healthcare professionals from the American Heart Association
AJ Lansky, JS Hochman, PA Ward, GS Mintz, R Fabunmi, PB Berger, ...
Circulation 111 (7), 940-953, 2005
3082005
Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males
D Del Gaudio, P Fang, F Scaglia, PA Ward, WJ Craigen, DG Glaze, ...
Genetics in Medicine 8 (12), 784-792, 2006
2972006
Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases
IB Van den Veyver, A Patel, CA Shaw, AN Pursley, SHL Kang, ...
Prenatal Diagnosis: Published in Affiliation With the International Society …, 2009
2532009
Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases
X Lu, CA Shaw, A Patel, J Li, ML Cooper, WR Wells, CM Sullivan, ...
PloS one 2 (3), e327, 2007
2482007
Reanalysis of clinical exome sequencing data
P Liu, L Meng, EA Normand, F Xia, X Song, A Ghazi, J Rosenfeld, ...
New England Journal of Medicine 380 (25), 2478-2480, 2019
2162019
Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization
T Sahoo, SW Cheung, P Ward, S Darilek, A Patel, D Del Gaudio, ...
Genetics in Medicine 8 (11), 719-727, 2006
2072006
Antiviral activity of hop constituents against a series of DNA and RNA viruses
VE Buckwold, RJH Wilson, A Nalca, BB Beer, TG Voss, JA Turpin, ...
Antiviral research 61 (1), 57-62, 2004
1852004
Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory
AK Petersen, SW Cheung, JL Smith, W Bi, PA Ward, S Peacock, ...
American journal of obstetrics and gynecology 217 (6), 691. e1-691. e6, 2017
1832017
MARRVEL: integration of human and model organism genetic resources to facilitate functional annotation of the human genome
J Wang, R Al-Ouran, Y Hu, SY Kim, YW Wan, MF Wangler, S Yamamoto, ...
The American Journal of Human Genetics 100 (6), 843-853, 2017
1752017
The undiagnosed diseases network: accelerating discovery about health and disease
RB Ramoni, JJ Mulvihill, DR Adams, P Allard, EA Ashley, JA Bernstein, ...
The American Journal of Human Genetics 100 (2), 185-192, 2017
1562017
Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with> 1000 cases and review of the literature
A Breman, AN Pursley, P Hixson, W Bi, P Ward, CA Bacino, C Shaw, ...
Prenatal diagnosis 32 (4), 351-361, 2012
1492012
Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder
EA Normand, A Braxton, S Nassef, PA Ward, F Vetrini, W He, V Patel, ...
Genome medicine 10, 1-14, 2018
1372018
Psychological aspects of genetic counseling. III. Management of guilt and shame
S Kessler, H Kessler, P Ward, JM Opitz
American journal of medical genetics 17 (3), 673-697, 1984
1221984
A syndromic neurodevelopmental disorder caused by de novo variants in EBF3
HT Chao, M Davids, E Burke, JG Pappas, JA Rosenfeld, AJ McCarty, ...
The American Journal of Human Genetics 100 (1), 128-137, 2017
1132017
A homozygous mutation in MSH6 causes Turcot syndrome
MR Hegde, B Chong, ME Blazo, LHE Chin, PA Ward, MM Chintagumpala, ...
Clinical cancer research 11 (13), 4689-4693, 2005
1082005
Genomic rearrangements of the APC tumor-suppressor gene in familial adenomatous polyposis
LK Su, G Steinbach, JC Sawyer, M Hindi, PA Ward, PM Lynch
Human genetics 106, 101-107, 2000
1052000
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Articles 1–20