Urvashi Surti
Urvashi Surti
Professor of Pathology
Verified email at mail.magee.edu
Cited by
Cited by
Large-scale genotyping of complex DNA
GC Kennedy, H Matsuzaki, S Dong, W Liu, J Huang, G Liu, X Su, M Cao, ...
Nature biotechnology 21 (10), 1233-1237, 2003
Resolving the complexity of the human genome using single-molecule sequencing
MJP Chaisson, J Huddleston, MY Dennis, PH Sudmant, M Malig, ...
Nature 517 (7536), 608-611, 2015
The syndromes of hydatidiform mole: I. Cytogenetic and morphologic correlations
AE Szulman, U Surti
American journal of obstetrics and gynecology 131 (6), 665-671, 1978
A recurrent 16p12. 1 microdeletion supports a two-hit model for severe developmental delay
S Girirajan, JA Rosenfeld, GM Cooper, F Antonacci, P Siswara, A Itsara, ...
Nature genetics 42 (3), 203-209, 2010
Content and organization of the human Ig VH locus: definition of three new VH families and linkage to the Ig CH locus.
JE Berman, SJ Mellis, R Pollock, CL Smith, H Suh, B Heinke, C Kowal, ...
The EMBO journal 7 (3), 727-738, 1988
The syndromes of hydatidiform mole: II. Morphologic evolution of the complete and partial mole
AE Szulman, U Surti
American journal of obstetrics and gynecology 132 (1), 20-27, 1978
Parental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry and association with the partial hydatidiform mole
MV Zaragoza, U Surti, RW Redline, E Millie, A Chakravarti, TJ Hassold
The American Journal of Human Genetics 66 (6), 1807-1820, 2000
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia
D Moreno-De-Luca, JG Mulle, EB Kaminsky, SJ Sanders, SM Myers, ...
The American Journal of Human Genetics 87 (5), 618-630, 2010
Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene.
CC Glenn, S Saitoh, MT Jong, MM Filbrandt, U Surti, DJ Driscoll, ...
American journal of human genetics 58 (2), 335, 1996
EWSR1‐CREB1 is the predominant gene fusion in angiomatoid fibrous histiocytoma
CR Antonescu, P Dal Cin, K Nafa, LA Teot, U Surti, CD Fletcher, ...
Genes, Chromosomes and Cancer 46 (12), 1051-1060, 2007
Discovery of a previously unrecognized microdeletion syndrome of 16p11. 2–p12. 2
BC Ballif, SA Hornor, E Jenkins, S Madan-Khetarpal, U Surti, KE Jackson, ...
Nature genetics 39 (9), 1071-1073, 2007
The clinical use of karyotyping spontaneous abortions
WA Hogge, AL Byrnes, MC Lanasa, U Surti
American journal of obstetrics and gynecology 189 (2), 397-400, 2003
Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients.
SL Christian, WP Robinson, B Huang, A Mutirangura, MR Line, M Nakao, ...
American journal of human genetics 57 (1), 40, 1995
The clinicopathologic profile of the partial hydatidiform mole.
AE Szulman, U Surti
Obstetrics and gynecology 59 (5), 597-602, 1982
Noninvasive prenatal diagnosis of a fetal microdeletion syndrome
D Peters, T Chu, SA Yatsenko, N Hendrix, WA Hogge, U Surti, K Bunce, ...
The New England journal of medicine 365 (19), 1847, 2011
High-resolution human genome structure by single-molecule analysis
B Teague, MS Waterman, S Goldstein, K Potamousis, S Zhou, S Reslewic, ...
Proceedings of the National Academy of Sciences 107 (24), 10848-10853, 2010
Genetics and biology of human ovarian teratomas. I. Cytogenetic analysis and mechanism of origin.
U Surti, L Hoffner, A Chakravarti, RE Ferrell
American journal of human genetics 47 (4), 635, 1990
Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28
E Pegoraro, J Whitaker, P Mowery-Rushton, U Surti, M Lanasa, ...
The American Journal of Human Genetics 61 (1), 160-170, 1997
Whole exome sequencing in a random sample of North American women with leiomyomas identifies MED12 mutations in majority of uterine leiomyomas
MM McGuire, A Yatsenko, L Hoffner, M Jones, U Surti, A Rajkovic
PloS one 7 (3), e33251, 2012
The physical organization of the human immunoglobulin heavy chain gene complex.
MA Walter, U Surti, MH Hofker, DW Cox
The EMBO journal 9 (10), 3303-3313, 1990
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