Chishimba Nathan Mowa

1.0k total citations
53 papers, 867 citations indexed

About

Chishimba Nathan Mowa is a scholar working on Molecular Biology, Obstetrics and Gynecology and Reproductive Medicine. According to data from OpenAlex, Chishimba Nathan Mowa has authored 53 papers receiving a total of 867 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 14 papers in Obstetrics and Gynecology and 13 papers in Reproductive Medicine. Recurrent topics in Chishimba Nathan Mowa's work include Angiogenesis and VEGF in Cancer (10 papers), Endometriosis Research and Treatment (10 papers) and Estrogen and related hormone effects (9 papers). Chishimba Nathan Mowa is often cited by papers focused on Angiogenesis and VEGF in Cancer (10 papers), Endometriosis Research and Treatment (10 papers) and Estrogen and related hormone effects (9 papers). Chishimba Nathan Mowa collaborates with scholars based in United States, Japan and South Africa. Chishimba Nathan Mowa's co-authors include Subrina Jesmin, R.E. Papka, Ichiro Sakuma, Yuichi Hattori, Akira Kitabatake, Hiroko Togashi, Takashi Miyauchi, Seiji Maeda, Michael M. Opata and Sharon Usip and has published in prestigious journals such as Brain Research, The FASEB Journal and Endocrinology.

In The Last Decade

Chishimba Nathan Mowa

50 papers receiving 841 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chishimba Nathan Mowa United States 18 192 190 136 134 132 53 867
Zofia Ostrowska Poland 21 292 1.5× 181 1.0× 95 0.7× 284 2.1× 97 0.7× 124 1.3k
Yun Shi China 18 204 1.1× 228 1.2× 183 1.3× 92 0.7× 111 0.8× 73 936
V. Minas Greece 16 121 0.6× 145 0.8× 59 0.4× 118 0.9× 183 1.4× 18 857
A. Faletti Argentina 17 110 0.6× 91 0.5× 88 0.6× 226 1.7× 139 1.1× 57 862
Andrés Quintanar‐Stephano Mexico 18 204 1.1× 248 1.3× 62 0.5× 74 0.6× 62 0.5× 82 1.0k
Motoo Shinoda Japan 15 146 0.8× 122 0.6× 60 0.4× 169 1.3× 47 0.4× 41 668
Wen Su United States 16 226 1.2× 132 0.7× 69 0.5× 202 1.5× 91 0.7× 29 743
Naoko Brown United States 23 362 1.9× 59 0.3× 164 1.2× 95 0.7× 208 1.6× 34 1.3k
Gustavo Ballejo Brazil 17 273 1.4× 217 1.1× 121 0.9× 283 2.1× 74 0.6× 51 1.1k
A. R. Genazzani Italy 22 181 0.9× 317 1.7× 230 1.7× 142 1.1× 127 1.0× 54 1.1k

Countries citing papers authored by Chishimba Nathan Mowa

Since Specialization
Citations

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

Fields of papers citing papers by Chishimba Nathan Mowa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chishimba Nathan Mowa. 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 Chishimba Nathan Mowa. The network helps show where Chishimba Nathan Mowa may publish in the future.

Co-authorship network of co-authors of Chishimba Nathan Mowa

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

All Works

20 of 20 papers shown
1.
Mowa, Chishimba Nathan, et al.. (2024). Moringa oleifera improves skeletal muscle metabolism and running performance in mice. South African Journal of Botany. 170. 61–70.
2.
Mowa, Chishimba Nathan, et al.. (2021). Plasmodium chabaudi Infection Alters Intestinal Morphology and Mucosal Innate Immunity in Moderately Malnourished Mice. Nutrients. 13(3). 913–913. 7 indexed citations
3.
4.
Tomasi, Jorgelina Barrios de, Michael M. Opata, & Chishimba Nathan Mowa. (2019). Immunity in the Cervix: Interphase between Immune and Cervical Epithelial Cells. Journal of Immunology Research. 2019. 1–13. 38 indexed citations
5.
Matsuishi, Yujiro, Subrina Jesmin, Satoru Kawano, et al.. (2016). Landiolol hydrochloride ameliorates acute lung injury in a rat model of early sepsis through the suppression of elevated levels of pulmonary endothelin-1. Life Sciences. 166. 27–33. 20 indexed citations
6.
7.
Jesmin, Subrina, Chishimba Nathan Mowa, Nobutake Shimojo, et al.. (2014). Dual blockade of endothelin action exacerbates up-regulated VEGF angiogenic signaling in the heart of lipopolysaccharide-induced endotoxemic rat model. Life Sciences. 118(2). 364–369. 5 indexed citations
8.
Donnelly, Siobhan, et al.. (2013). Vascular endothelial growth factor induces growth of uterine cervix and immune cell recruitment in mice. Journal of Endocrinology. 217(1). 83–94. 10 indexed citations
9.
Jesmin, Subrina, Chishimba Nathan Mowa, Sayeeda Sultana, et al.. (2010). VEGF signaling is disrupted in the hearts of mice lacking estrogen receptor alpha. European Journal of Pharmacology. 641(2-3). 168–178. 26 indexed citations
10.
Jesmin, Subrina, Chishimba Nathan Mowa, Sayeeda Sultana, et al.. (2010). Estrogen receptor alpha and beta are both involved in the cerebral VEGF/Akt/NO pathway and cerebral angiogenesis in female mice. Biomedical Research. 31(6). 337–346. 17 indexed citations
11.
Mowa, Chishimba Nathan, et al.. (2007). Estrogen enhances penile healing and VEGF expression in rats. The FASEB Journal. 21(6).
12.
Jesmin, Subrina, Seiji Maeda, Chishimba Nathan Mowa, et al.. (2007). Antagonism of endothelin action normalizes altered levels of VEGF and its signaling in the brain of stroke-prone spontaneously hypertensive rat. European Journal of Pharmacology. 574(2-3). 158–171. 9 indexed citations
13.
Aizawa, Katsuji, Motoyuki Iemitsu, Seiji Maeda, et al.. (2006). Expression of steroidogenic enzymes and synthesis of sex steroid hormones from DHEA in skeletal muscle of rats. American Journal of Physiology-Endocrinology and Metabolism. 292(2). E577–E584. 75 indexed citations
14.
Mowa, Chishimba Nathan, et al.. (2006). The penis: a new target and source of estrogen in male reproduction.. PubMed. 21(1). 53–67. 22 indexed citations
15.
Jesmin, Subrina, Sohel Zaedi, Nobutake Shimojo, et al.. (2006). Endothelin antagonism normalizes VEGF signaling and cardiac function in STZ-induced diabetic rat hearts. American Journal of Physiology-Endocrinology and Metabolism. 292(4). E1030–E1040. 45 indexed citations
16.
Mowa, Chishimba Nathan, Subrina Jesmin, Ichiro Sakuma, et al.. (2003). Vascular endothelial growth factor (VEGF), its receptors (KDR and Flt-1) and eNOS are up-regulated in the rat uterine cervix during pregnancy. 6. 1 indexed citations
17.
18.
Jesmin, Subrina, Yuichi Hattori, Ichiro Sakuma, et al.. (2003). Estrogen Deprivation and Replacement Modulate Cerebral Capillary Density With Vascular Expression of Angiogenic Molecules in Middle-Aged Female Rats. Journal of Cerebral Blood Flow & Metabolism. 181–189. 14 indexed citations
19.
Mowa, Chishimba Nathan, Sharon Usip, J. Collins, et al.. (2003). The effects of pregnancy and estrogen on the expression of calcitonin gene-related peptide (CGRP) in the uterine cervix, dorsal root ganglia and spinal cord. Peptides. 24(8). 1163–1174. 40 indexed citations
20.
Yanase, Haruko, Chishimba Nathan Mowa, Nobuya Inagaki, Susumu Seino, & Toshihiko Iwanaga. (1998). CELLULAR DISTRIBUTION OF SULFONYLUREA RECEPTOR 2 mRNA IN THE OVARY AND TESTIS OE RATS. Biomedical Research. 19(3). 199–204. 2 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Zofia Ostrowska Breakdown of academic impact, for papers by Yun Shi Breakdown of academic impact, for papers by V. Minas Breakdown of academic impact, for papers by A. Faletti Breakdown of academic impact, for papers by Andrés Quintanar‐Stephano Breakdown of academic impact, for papers by Motoo Shinoda Breakdown of academic impact, for papers by Wen Su Breakdown of academic impact, for papers by Naoko Brown Breakdown of academic impact, for papers by Gustavo Ballejo Breakdown of academic impact, for papers by A. R. Genazzani
Rankless by CCL
2026