Reference sequence (RefSeq) database at NCBI: current status, taxonomic expansion, and functional annotation NA O'Leary, MW Wright, JR Brister, S Ciufo, D Haddad, R McVeigh, ... Nucleic acids research 44 (D1), D733-D745, 2016 | 6311 | 2016 |
RefSeq: an update on mammalian reference sequences KD Pruitt, GR Brown, SM Hiatt, F Thibaud-Nissen, A Astashyn, ... Nucleic acids research 42 (D1), D756-D763, 2014 | 1168 | 2014 |
Mendelian randomization E Birney Cold Spring Harbor perspectives in medicine 12 (4), a041302, 2022 | 564 | 2022 |
A joint NCBI and EMBL-EBI transcript set for clinical genomics and research J Morales, S Pujar, JE Loveland, A Astashyn, R Bennett, A Berry, E Cox, ... Nature 604 (7905), 310-315, 2022 | 324 | 2022 |
Database resources of the National Center for Biotechnology Information in 2023 EW Sayers, EE Bolton, JR Brister, K Canese, J Chan, DC Comeau, ... Nucleic acids research 51 (D1), D29, 2023 | 272 | 2023 |
Current status and new features of the Consensus Coding Sequence database CM Farrell, NA O’Leary, RA Harte, JE Loveland, LG Wilming, C Wallin, ... Nucleic acids research 42 (D1), D865-D872, 2014 | 165 | 2014 |
Consensus coding sequence (CCDS) database: a standardized set of human and mouse protein-coding regions supported by expert curation S Pujar, NA O’Leary, CM Farrell, JE Loveland, JM Mudge, C Wallin, ... Nucleic Acids Research 46 (D1), D221-D228, 2018 | 133 | 2018 |
Database resources of the national center for biotechnology information EW Sayers, J Beck, EE Bolton, JR Brister, J Chan, DC Comeau, R Connor, ... Nucleic Acids Research 52 (D1), D33, 2024 | 107 | 2024 |
The status of the human gene catalogue P Amaral, S Carbonell-Sala, FM De La Vega, T Faial, A Frankish, ... Nature 622 (7981), 41-47, 2023 | 96 | 2023 |
A single base pair mutation encoding a premature stop codon in the MIS type II receptor is responsible for canine persistent Müllerian duct syndrome X Wu, S Wan, S Pujar, ME Haskins, DH Schlafer, MM Lee, ... Journal of andrology 30 (1), 46-56, 2009 | 70 | 2009 |
A molecular diagnostic test for persistent Müllerian duct syndrome in miniature schnauzer dogs S Pujar, VN Meyers-Wallen Sexual Development 3 (6), 326-328, 2010 | 31 | 2010 |
Exclusion of Candidate Genes for Canine SRY-Negative XX Sex Reversal K Kothapalli, E Kirkness, S Pujar, R Van Wormer, VN Meyers-Wallen Journal of Heredity 96 (7), 759-763, 2005 | 27 | 2005 |
Exclusion of Lhx9 as a Candidate Gene for Sry-Negative XX Sex Reversal in the American Cocker Spaniel Model S Pujar, KS Kothapalli, E Kirkness, RH Van Wormer, VN Meyers-Wallen Journal of Heredity 96 (4), 452-454, 2005 | 27 | 2005 |
Mutations in the RSPO1 coding region are not the main cause of canine SRY-negative XX sex reversal in several breeds L De Lorenzi, D Groppetti, S Arrighi, S Pujar, L Nicoloso, L Molteni, ... Sexual Development 2 (2), 84-95, 2008 | 26 | 2008 |
Mouse genome annotation by the RefSeq project KM McGarvey, T Goldfarb, E Cox, CM Farrell, T Gupta, VS Joardar, ... Mammalian Genome 26, 379-390, 2015 | 24 | 2015 |
A curated catalog of canine and equine keratin genes P Balmer, A Bauer, S Pujar, KM McGarvey, M Welle, A Galichet, EJ Müller, ... PloS one 12 (8), e0180359, 2017 | 20 | 2017 |
Linkage to CFA29 Detected in a Genome-Wide Linkage Screen of a Canine Pedigree Segregating Sry-Negative XX Sex Reversal S Pujar, KSD Kothapalli, HHH Göring, VN Meyers-Wallen Journal of heredity 98 (5), 438-444, 2007 | 20 | 2007 |
XX Disorder of Sex Development is associated with an insertion on chromosome 9 and downregulation of RSPO1 in dogs (Canis lupus familiaris) VN Meyers-Wallen, AR Boyko, CG Danko, JK Grenier, JG Mezey, ... PLoS One 12 (10), e0186331, 2017 | 19 | 2017 |
Exclusion ofWT1as a candidate gene for canineSRY-negative XX sex reversal. KSD Kothapalli, EF Kirkness, S Pujar, VN Meyers-Wallen Animal genetics 35 (6), 2004 | 11 | 2004 |
Sequence variations in equine candidate genes For XX and XY inherited disorders of sexual development S Pujar, VN Meyers‐Wallen Reproduction in domestic animals 47 (5), 827-834, 2012 | 10 | 2012 |