Juan C. Perín

2.4k total citations
17 papers, 834 citations indexed

About

Juan C. Perín is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Juan C. Perín has authored 17 papers receiving a total of 834 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Hematology. Recurrent topics in Juan C. Perín's work include Acute Myeloid Leukemia Research (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (3 papers). Juan C. Perín is often cited by papers focused on Acute Myeloid Leukemia Research (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (3 papers). Juan C. Perín collaborates with scholars based in United States, Argentina and France. Juan C. Perín's co-authors include Håkon Håkonarson, Hongbo Xie, Xiaowu Gai, Tamim H. Shaikh, Jaclyn A. Biegel, Eric Rappaport, Angela J. Sievert, Vincent Procaccio, Eric M. Jackson and Laura Tooke and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Juan C. Perín

17 papers receiving 820 citations

Peers

Countries citing papers authored by Juan C. Perín

Since Specialization

Citations

This map shows the geographic impact of Juan C. Perín'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 Juan C. Perín with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Juan C. Perín more than expected).

Fields of papers citing papers by Juan C. Perín

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Juan C. Perín. 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 Juan C. Perín. The network helps show where Juan C. Perín may publish in the future.

Co-authorship network of co-authors of Juan C. Perín

This figure shows the co-authorship network connecting the top 25 collaborators of Juan C. Perín. A scholar is included among the top collaborators of Juan C. Perín 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 Juan C. Perín. Juan C. Perín is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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17 of 17 papers shown

#	Work	Indexed citations
1	Clonal hematopoiesis in patients with dyskeratosis congenita 2016 ·American Journal of Hematology ·Nieves Perdigones, Juan C. Perín, (unknown), Peter Nicholas, Jaclyn A. Biegel, Philip J. Mason, Daria V. Babushok, Monica Bessler	41
2	Emergence of clonal hematopoiesis in the majority of patients with acquired aplastic anemia 2015 ·Cancer Genetics ·Daria V. Babushok, Nieves Perdigones, Juan C. Perín, Timothy S. Olson, Wenda Ye, Jacquelyn J. Roth, Curt Lind, (unknown), Yimei Li, Helge Hartung, Michele Paessler, Dale Frank, Hongbo Xie, (unknown), (unknown), Gregory M. Podsakoff, Dimitrios Monos, Jaclyn A. Biegel, Philip J. Mason, Monica Bessler	78
3	Abstract 2977: Most patients with acquired aplastic anemia develop clonal hematopoiesis early in disease 2015 ·Cancer Research ·Daria V. Babushok, Nieves Perdigones, Juan C. Perín, Timothy S. Olson, Wenda Ye, Jacquelyn J. Roth, Curt Lind, (unknown), Yimei Li, Helge Hartung, Michele Paessler, Dale Frank, Hongbo Xie, Tracy Busse, (unknown), Gregory M. Podsakoff, Dimitrios Monos, Jaclyn A. Biegel, Philip J. Mason, Monica Bessler	1
4	An Acquired Mutation in Deubiquitinating Enzyme USP11 Associated with Clonal Hematopoiesis in Diamond Blackfan Anemia 2014 ·Blood ·Nieves Perdigones, Daria V. Babushok, Lifeng Tian, Jonathan P. Bradfield, Cecilia E Kim, Juan C. Perín, Håkon Håkonarson, Monica Bessler, Philip J. Mason	1
5	Progressive increase in mtDNA 3243A>G heteroplasmy causes abrupt transcriptional reprogramming 2014 ·Proceedings of the National Academy of Sciences ·Martin Picard, Jiangwen Zhang, Saege Hancock, Olga Derbeneva, Ryan Golhar, Paweł Golik, Sean F. O’Hearn, Shawn Levy, Prasanth Potluri, Maria Lvova, Antonio Dávila, Chun Shi Lin, Juan C. Perín, Eric Rappaport, Håkon Håkonarson, Ian A. Trounce, Vincent Procaccio, Douglas C. Wallace	231
6	Single nucleotide polymorphism array analysis of bone marrow failure patients reveals characteristic patterns of genetic changes 2013 ·British Journal of Haematology ·Daria V. Babushok, Hongbo Xie, Jacquelyn J. Roth, Nieves Perdigones, Timothy S. Olson, (unknown), Xiaowu Gai, Juan C. Perín, Yimei Li, Michele Paessler, Håkon Håkonarson, Gregory M. Podsakoff, Philip J. Mason, Jaclyn A. Biegel, Monica Bessler	15
7	Efficient digest of high-throughput sequencing data in a reproducible report 2013 ·BMC Bioinformatics ·Zhe Zhang, Jeremy Leipzig, Ariella Sasson, Angela M Yu, Juan C. Perín, Hongbo Xie, Mahdi Sarmady, Patrick V. Warren, Peter S. White	8
8	Rare structural variation of synapse and neurotransmission genes in autism 2011 ·Molecular Psychiatry ·Xiaowu Gai, Hongbo Xie, Juan C. Perín, Nagahide Takahashi, Kevin J. Murphy, (unknown), Monica D’Arcy, (unknown), Elizabeth Goldmuntz, Dorothy E. Grice, Tamim H. Shaikh, Håkon Håkonarson, Joseph D. Buxbaum, Josephine Elia, Peter S. White	118
9	Genome-wide analysis of interferon regulatory factor I binding in primary human monocytes 2011 ·Gene ·Lihua Shi, Juan C. Perín, Jeremy Leipzig, Zhe Zhang, Kathleen E. Sullivan	33
10	Mitochondrial genome sequence analysis: A custom bioinformatics pipeline substantially improves Affymetrix MitoChip v2.0 call rate and accuracy 2011 ·BMC Bioinformatics ·Hongbo Xie, Juan C. Perín, Theodore G. Schurr, Matthew C. Dulik, Sergey Zhadanov, Joseph A. Baur, Michael P. King, Emily Place, Colleen Clarke, Michael Grauer, Jonathan Schug, Avni Santani, (unknown), Cecilia Kim, Vincent Procaccio, Håkon Håkonarson, Xiaowu Gai, Marni J. Falk	17
11	High-Resolution genomic arrays identify CNVs that phenocopy the chromosome 22q11.2 deletion syndrome 2010 ·Human Mutation ·Tracy Busse, John M. Graham, Gerald L. Feldman, Juan C. Perín, (unknown), Robert C. Knowlton, Eric Rappaport, Beverly S. Emanuel, Deborah A. Driscoll, Sulagna C. Saitta	15
12	CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics 2010 ·BMC Bioinformatics ·Xiaowu Gai, Juan C. Perín, Kevin J. Murphy, (unknown), Monica D’Arcy, (unknown), Hongbo Xie, Eric Rappaport, Tamim H. Shaikh, Peter S. White	42
13	Cytokine-Induced Monocyte Characteristics in SLE 2010 ·SHILAP Revista de lepidopterología ·Zhe Zhang, Kelly Maurer, Juan C. Perín, Song Li, Kathleen E. Sullivan	21
14	Genomic Analysis Using High-Density Single Nucleotide Polymorphism-Based Oligonucleotide Arrays and Multiplex Ligation-Dependent Probe Amplification Provides a Comprehensive Analysis of INI1/SMARCB1 in Malignant Rhabdoid Tumors 2009 ·Clinical Cancer Research ·Eric M. Jackson, Angela J. Sievert, Xiaowu Gai, Håkon Håkonarson, Alexander R. Judkins, Laura Tooke, Juan C. Perín, Hongbo Xie, Tamim H. Shaikh, Jaclyn A. Biegel	142
15	A 3.1-Mb microdeletion of 3p21.31 associated with cortical blindness, cleft lip, CNS abnormalities, and developmental delay 2008 ·European Journal of Medical Genetics ·Chad Haldeman‐Englert, Xiaowu Gai, Juan C. Perín, (unknown), Sara Halbach, Elizabeth A. Geiger, Donna M. McDonald‐McGinn, Håkon Håkonarson, Elaine H. Zackai, Tamim H. Shaikh	15
16	Systematic epitope analysis of the p26 EIAV core protein 2007 ·Journal of Molecular Recognition ·(unknown), (unknown), Juan C. Perín, Leila Maria Beltramini, Ileana Malán Borel, Ronald Frank, Georgina Tonarelli	15
17	Monitoring substrate and products in a bioprocess with FTIR spectroscopy coupled to artificial neural networks enhanced with a genetic-algorithm-based method for wavelength selection 2005 ·Talanta ·(unknown), Juan C. Perín, (unknown), Héctor C. Goicoechea	41

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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