Tina Graves

29.6k total citations
35 papers, 3.5k citations indexed

About

Tina Graves is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Tina Graves has authored 35 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 25 papers in Molecular Biology and 24 papers in Plant Science. Recurrent topics in Tina Graves's work include Chromosomal and Genetic Variations (24 papers), Genomic variations and chromosomal abnormalities (18 papers) and Genomics and Chromatin Dynamics (12 papers). Tina Graves is often cited by papers focused on Chromosomal and Genetic Variations (24 papers), Genomic variations and chromosomal abnormalities (18 papers) and Genomics and Chromatin Dynamics (12 papers). Tina Graves collaborates with scholars based in United States, Italy and United Kingdom. Tina Graves's co-authors include Richard K. Wilson, Evan E. Eichler, Maika Malig, Wesley C. Warren, Mario Ventura, Helen Skaletsky, David C. Page, Tatyana Pyntikova, Jeffrey M. Kidd and Francesca Antonacci and has published in prestigious journals such as Nature, Cell and Nature Genetics.

In The Last Decade

Tina Graves

35 papers receiving 3.4k citations

Peers

Countries citing papers authored by Tina Graves

Since Specialization

Citations

This map shows the geographic impact of Tina Graves's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Tina Graves with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tina Graves more than expected).

Fields of papers citing papers by Tina Graves

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tina Graves. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Tina Graves. The network helps show where Tina Graves may publish in the future.

Co-authorship network of co-authors of Tina Graves

This figure shows the co-authorship network connecting the top 25 collaborators of Tina Graves. A scholar is included among the top collaborators of Tina Graves based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Tina Graves. Tina Graves is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	A new domestic cat genome assembly based on long sequence reads empowers feline genomic medicine and identifies a novel gene for dwarfism 2020 ·PLoS Genetics ·Reuben M. Buckley, Brian W. Davis, Wesley Brashear, Fabiana Farias, Kei Kuroki, Tina Graves, LaDeana Hillier, Milinn Kremitzki, Gang Li, (unknown), (unknown), Chad Tomlinson, Leslie A. Lyons, William J. Murphy, Wesley C. Warren	82
2	Interchromosomal core duplicons drive both evolutionary instability and disease susceptibility of the Chromosome 8p23.1 region 2016 ·Genome Research ·Kiana Mohajeri, Stuart Cantsilieris, John Huddleston, Bradley J. Nelson, Bradley P. Coe, Catarina D. Campbell, Carl Baker, Lana Harshman, Katherine M. Munson, Zev Kronenberg, Milinn Kremitzki, Archana N. Raja, Claudia Rita Catacchio, Tina Graves, Richard K. Wilson, Mario Ventura, Evan E. Eichler	20
3	Finished sequence and assembly of the DUF1220-rich 1q21 region using a haploid human genome 2014 ·BMC Genomics ·Majesta O’Bleness, (unknown), C. Michael Dickens, David P. Astling, Derek Albracht, Angel C. Y. Mak, Yvonne Y. Y. Lai, Chin Jia Lin, Catherine Chu, Tina Graves, Pui–Yan Kwok, Richard K. Wilson, James M. Sikela	35
4	Reconstructing complex regions of genomes using long-read sequencing technology 2014 ·Genome Research ·John Huddleston, Swati Ranade, Maika Malig, Francesca Antonacci, Mark Chaisson, Lawrence Hon, Peter H. Sudmant, Tina Graves, Can Alkan, Megan Y. Dennis, Richard K. Wilson, Stephen W. Turner, Jonas Korlach, Evan E. Eichler	179
5	Subtelomeric CTCF and cohesin binding site organization using improved subtelomere assemblies and a novel annotation pipeline 2014 ·Genome Research ·Nicholas Stong, Zhong Deng, Ravi Gupta, Sufen Hu, (unknown), Amber K. Weiner, Evan E. Eichler, Tina Graves, Catrina C. Fronick, Laura Courtney, Richard K. Wilson, Paul M. Lieberman, Ramana V. Davuluri, Harold Riethman	51
6	Independent specialization of the human and mouse X chromosomes for the male germ line 2013 ·Nature Genetics ·Jacob L. Mueller, Helen Skaletsky, Laura G. Brown, Sara Zaghlul, Susan M. Rock, Tina Graves, Katherine A. Auger, Wesley C. Warren, Richard K. Wilson, David C. Page	2
7	Complete Haplotype Sequence of the Human Immunoglobulin Heavy-Chain Variable, Diversity, and Joining Genes and Characterization of Allelic and Copy-Number Variation 2013 ·The American Journal of Human Genetics ·Corey T. Watson, Karyn Meltz Steinberg, John Huddleston, Robin M. Warren, Maika Malig, Jacqueline E. Schein, A. Jeremy Willsey, Jeffrey B. Joy, Jamie K. Scott, Tina Graves, Richard K. Wilson, Robert A. Holt, Evan E. Eichler, Felix Breden	154
8	Gorilla genome structural variation reveals evolutionary parallelisms with chimpanzee 2011 ·Genome Research ·Mario Ventura, Claudia Rita Catacchio, Can Alkan, Tomàs Marquès‐Bonet, Saba Sajjadian, Tina Graves, Fereydoun Hormozdiari, Arcadi Navarro, Maika Malig, Carl Baker, Choli Lee, Emily H. Turner, Lin Chen, Jeffrey M. Kidd, Nicoletta Archidiacono, Jay Shendure, Richard K. Wilson, Evan E. Eichler	55
9	Convergent evolution of chicken Z and human X chromosomes by expansion and gene acquisition 2010 ·Nature ·Daniel W. Bellott, Helen Skaletsky, Tatyana Pyntikova, Elaine R. Mardis, Tina Graves, Colin Kremitzki, Laura G. Brown, Steve Rozen, Wesley C. Warren, Richard K. Wilson, David C. Page	168
10	Gene duplication and fragmentation in the zebra finch major histocompatibility complex 2010 ·BMC Biology ·Christopher N. Balakrishnan, Robert Ekblom, Martin A. Volker, Helena Westerdahl, (unknown), (unknown), David W. Burt, Tina Graves, Darren K. Griffin, Wesley C. Warren, Scott V. Edwards	109
11	The Physical and Genetic Framework of the Maize B73 Genome 2009 ·PLoS Genetics ·Fusheng Wei, Jianwei Zhang, Shiguo Zhou, Ruifeng He, Mary Schaeffer, Kristi Collura, David Kudrna, Ben Faga, Marina Wissotski, Wolfgang Golser, Susan M. Rock, Tina Graves, Robert S. Fulton, E. H. Coe, Patrick S. Schnable, David C. Schwartz, Doreen Ware, Sandra W. Clifton, Richard K. Wilson, Rod A. Wing	78
12	A burst of segmental duplications in the genome of the African great ape ancestor 2009 ·Nature ·Tomàs Marquès‐Bonet, Jeffrey M. Kidd, Mario Ventura, Tina Graves, Ze Cheng, LaDeana Hillier, Zhaoshi Jiang, Carl Baker, (unknown), Lucinda A. Fulton, Can Alkan, Gozde Aksay, Santhosh Girirajan, Priscillia Siswara, Lin Chen, Maria Francesca Cardone, Arcadi Navarro, Elaine R. Mardis, Richard K. Wilson, Evan E. Eichler	168
13	Sequencing human–gibbon breakpoints of synteny reveals mosaic new insertions at rearrangement sites 2008 ·Genome Research ·Santhosh Girirajan, Lin Chen, Tina Graves, Tomàs Marquès‐Bonet, Mario Ventura, Catrina C. Fronick, Lucinda A. Fulton, Mariano Rocchi, Robert S. Fulton, Richard K. Wilson, Elaine R. Mardis, Evan E. Eichler	26
14	Gene discovery and comparative analysis of X-degenerate genes from the domestic cat Y chromosome☆☆Sequence data from this article have been deposited with the EMBL/GenBank Data Libraries under Accession No. EU879967-EU879988. 2008 ·Genomics ·Alison J. Pearks Wilkerson, Terje Raudsepp, Tina Graves, Derek Albracht, Wesley C. Warren, Bhanu P. Chowdhary, Loren C. Skow, William J. Murphy	41
15	Haplotype sorting using human fosmid clone end-sequence pairs 2008 ·Genome Research ·Jeffrey M. Kidd, Ze Cheng, Tina Graves, Bob Fulton, Richard K. Wilson, Evan E. Eichler	18
16	Punctuated duplication seeding events during the evolution of human chromosome 2p11 2005 ·Genome Research ·Julie E. Horvath, Cassandra Gulden, Rhea U. Vallente, (unknown), Mario Ventura, John D. McPherson, Tina Graves, Richard K. Wilson, Stuart Schwartz, Mariano Rocchi, Evan E. Eichler	29
17	Conservation of Y-linked genes during human evolution revealed by comparative sequencing in chimpanzee 2005 ·Nature ·Jennifer F. Hughes, Helen Skaletsky, Tatyana Pyntikova, Patrick Minx, Tina Graves, Steve Rozen, Richard K. Wilson, David C. Page	128
18	A genome-wide comparison of recent chimpanzee and human segmental duplications 2005 ·Nature ·Ze Cheng, Mario Ventura, Xinwei She, Philipp Khaitovich, Tina Graves, Kazutoyo Osoegawa, Deanna M. Church, Pieter DeJong, Richard K. Wilson, Svante Pääbo, Mariano Rocchi, Evan E. Eichler	287
19	Analysis of Human mRNAs With the Reference Genome Sequence Reveals Potential Errors, Polymorphisms, and RNA Editing 2004 ·Genome Research ·Terrence S. Furey, Mark Diekhans, Yontao Lu, Tina Graves, (unknown), (unknown), LaDeana W. Hillier, Richard K. Wilson, David Haussler	29
20	Surveying Saccharomyces Genomes to Identify Functional Elements by Comparative DNA Sequence Analysis 2001 ·Genome Research ·Paul F. Cliften, LaDeana W. Hillier, Lucinda Fulton, Tina Graves, Tracie L. Miner, Warren Gish, R Waterston, Mark Johnston	194

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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