Matthew Petitt

2.3k total citations · 1 hit paper
28 papers, 1.7k citations indexed

About

Matthew Petitt is a scholar working on Pediatrics, Perinatology and Child Health, Epidemiology and Obstetrics and Gynecology. According to data from OpenAlex, Matthew Petitt has authored 28 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Pediatrics, Perinatology and Child Health, 11 papers in Epidemiology and 11 papers in Obstetrics and Gynecology. Recurrent topics in Matthew Petitt's work include Cytomegalovirus and herpesvirus research (11 papers), Pregnancy and preeclampsia studies (7 papers) and Prenatal Screening and Diagnostics (7 papers). Matthew Petitt is often cited by papers focused on Cytomegalovirus and herpesvirus research (11 papers), Pregnancy and preeclampsia studies (7 papers) and Prenatal Screening and Diagnostics (7 papers). Matthew Petitt collaborates with scholars based in United States, Japan and Slovakia. Matthew Petitt's co-authors include Lenore Pereira, Takako Tabata, June Fang-Hoover, Henry Puerta‐Guardo, Eva Harris, Daniela Michlmayr, Chunling Wang, Nihar R. Nayak, J.H. McKerrow and Susan Hannah Allen and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and The Journal of Experimental Medicine.

In The Last Decade

Matthew Petitt

28 papers receiving 1.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Zika Virus Targets Different Primary Human Placental Cells, Suggesting Two Routes for Vertical Transmission

2016 372 citations Takako Tabata, Matthew Petitt et al. Cell Host & Microbe profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Matthew Petitt United States	23	623	509	508	506	334	28	1.7k
Daniel Chai Kenya	21	62 0.1×	155 0.3×	641 1.3×	287 0.6×	149 0.4×	68	1.7k
Jonathan E. Boyson United States	27	216 0.3×	311 0.6×	375 0.7×	408 0.8×	49 0.1×	55	3.2k
Robert Markham Australia	34	196 0.3×	117 0.2×	2.0k 4.0×	639 1.3×	45 0.1×	103	3.5k
Myrna M. Miller United States	18	259 0.4×	206 0.4×	81 0.2×	75 0.1×	137 0.4×	52	1.1k
Sandra Blaise‐Boisseau France	16	267 0.4×	94 0.2×	108 0.2×	90 0.2×	132 0.4×	34	1.2k
Jianhong Zhang Canada	27	49 0.1×	296 0.6×	875 1.7×	447 0.9×	253 0.8×	48	2.3k
Daniel Nagore Spain	16	219 0.4×	85 0.2×	73 0.1×	126 0.2×	93 0.3×	43	1.2k
Kendra M. Quicke United States	12	925 1.5×	404 0.8×	113 0.2×	1.0k 2.0×	59 0.2×	17	1.7k
Derek J. Platt United States	13	1.3k 2.2×	595 1.2×	104 0.2×	1.5k 2.9×	62 0.2×	17	2.0k
Carmen Rubio Spain	37	210 0.3×	182 0.4×	124 0.2×	1.7k 3.4×	2.1k 6.4×	108	3.7k

Countries citing papers authored by Matthew Petitt

Since Specialization

Citations

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

Fields of papers citing papers by Matthew Petitt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew Petitt. 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 Matthew Petitt. The network helps show where Matthew Petitt may publish in the future.

Co-authorship network of co-authors of Matthew Petitt

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew Petitt. A scholar is included among the top collaborators of Matthew Petitt 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 Matthew Petitt. Matthew Petitt 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

Fan, Xiujun, et al.. (2021). VEGF Maintains Maternal Vascular Space Homeostasis in the Mouse Placenta through Modulation of Trophoblast Giant Cell Functions. Biomolecules. 11(7). 1062–1062. 16 indexed citations

Tabata, Takako, Matthew Petitt, June Fang-Hoover, & Lenore Pereira. (2019). Survey of cellular immune responses to human cytomegalovirus infection in the microenvironment of the uterine–placental interface. Medical Microbiology and Immunology. 208(3-4). 475–485. 17 indexed citations

Puerta‐Guardo, Henry, Takako Tabata, Matthew Petitt, et al.. (2019). Zika Virus Nonstructural Protein 1 Disrupts Glycosaminoglycans and Causes Permeability in Developing Human Placentas. The Journal of Infectious Diseases. 221(2). 313–324. 40 indexed citations

Petitt, Matthew, Takako Tabata, Henry Puerta‐Guardo, Eva Harris, & Lenore Pereira. (2017). Zika virus infection of first-trimester human placentas: utility of an explant model of replication to evaluate correlates of immune protection ex vivo. Current Opinion in Virology. 27. 48–56. 23 indexed citations

Pereira, Lenore, Takako Tabata, Matthew Petitt, & June Fang-Hoover. (2017). Congenital cytomegalovirus infection undermines early development and functions of the human placenta. Placenta. 59. S8–S16. 34 indexed citations

Tabata, Takako, Matthew Petitt, Henry Puerta‐Guardo, et al.. (2017). Zika Virus Replicates in Proliferating Cells in Explants From First-Trimester Human Placentas, Potential Sites for Dissemination of Infection. The Journal of Infectious Diseases. 217(8). 1202–1213. 54 indexed citations

Tabata, Takako, Matthew Petitt, June Fang-Hoover, Martin Zydek, & Lenore Pereira. (2016). Persistent Cytomegalovirus Infection in Amniotic Membranes of the Human Placenta. American Journal Of Pathology. 186(11). 2970–2986. 26 indexed citations

Tabata, Takako, Matthew Petitt, Henry Puerta‐Guardo, et al.. (2016). Zika Virus Targets Different Primary Human Placental Cells, Suggesting Two Routes for Vertical Transmission. Cell Host & Microbe. 20(2). 155–166. 372 indexed citations breakdown →

Tabata, Takako, Matthew Petitt, Martin Zydek, et al.. (2015). Human Cytomegalovirus Infection Interferes with the Maintenance and Differentiation of Trophoblast Progenitor Cells of the Human Placenta. Journal of Virology. 89(9). 5134–5147. 56 indexed citations

10.

Pereira, Lenore, Matthew Petitt, Alex Fong, et al.. (2014). Intrauterine Growth Restriction Caused by Underlying Congenital Cytomegalovirus Infection. The Journal of Infectious Diseases. 209(10). 1573–1584. 81 indexed citations

11.

Pereira, Lenore, Matthew Petitt, & Takako Tabata. (2013). Cytomegalovirus Infection and Antibody Protection of the Developing Placenta. Clinical Infectious Diseases. 57(suppl_4). S174–S177. 21 indexed citations

12.

Tabata, Takako, Matthew Petitt, June Fang-Hoover, et al.. (2012). Cytomegalovirus Impairs Cytotrophoblast-Induced Lymphangiogenesis and Vascular Remodeling in an in Vivo Human Placentation Model. American Journal Of Pathology. 181(5). 1540–1559. 35 indexed citations

13.

Petitt, Matthew, et al.. (1997). MUCLIN expression in the cystic fibrosis transmembrane conductance regulator knockout mouse. Gastroenterology. 113(2). 521–532. 27 indexed citations

14.

Andrew, Deborah J., Michael A. Horner, Matthew Petitt, Sarah M. Smolik, & Matthew P. Scott. (1994). Setting limits on homeotic gene function: restraint of Sex combs reduced activity by teashirt and other homeotic genes.. The EMBO Journal. 13(5). 1132–1144. 102 indexed citations

15.

Fishelson, Zvi, Payman Amiri, Daniel S. Friend, et al.. (1992). Schistosoma mansoni: Cell-specific expression and secretion of a serine protease during development of cercariae. Experimental Parasitology. 75(1). 87–98. 58 indexed citations

16.

Bermingham, John R., Alfonso Martínez Arias, Matthew Petitt, & Matthew P. Scott. (1990). Different patterns of transcription from the two Antennapedia promoters during Drosophila embryogenesis. Development. 109(3). 553–566. 36 indexed citations

17.

Newport, George, James H. McKerrow, Richard C. Hedstrom, et al.. (1988). Cloning of the proteinase that facilitates infection by schistosome parasites.. Journal of Biological Chemistry. 263(26). 13179–13184. 62 indexed citations

18.

Keene, William E., Matthew Petitt, Susan Hannah Allen, & J.H. McKerrow. (1986). The major neutral proteinase of Entamoeba histolytica.. The Journal of Experimental Medicine. 163(3). 536–549. 164 indexed citations

19.

Lindquist, Robert N., Alfred W. Senft, Matthew Petitt, & James H. McKerrow. (1986). Schistosoma mansoni: Purification and characterization of the major acidic proteinase from adult worms. Experimental Parasitology. 61(3). 398–404. 36 indexed citations

20.

Petitt, Matthew, et al.. (1986). Preparation of Mouse Monoclonal Antibodies and Evidence for a Host Immune Response to the Preacetabular Gland Proteinase of Schistosoma Mansoni Cercariae. American Journal of Tropical Medicine and Hygiene. 35(3). 536–543. 24 indexed citations

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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