Natalie M. Gallant

1.6k total citations
18 papers, 922 citations indexed

About

Natalie M. Gallant is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Natalie M. Gallant has authored 18 papers receiving a total of 922 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Clinical Biochemistry and 4 papers in Genetics. Recurrent topics in Natalie M. Gallant's work include Metabolism and Genetic Disorders (6 papers), Genomics and Rare Diseases (3 papers) and Mitochondrial Function and Pathology (3 papers). Natalie M. Gallant is often cited by papers focused on Metabolism and Genetic Disorders (6 papers), Genomics and Rare Diseases (3 papers) and Mitochondrial Function and Pathology (3 papers). Natalie M. Gallant collaborates with scholars based in United States, United Kingdom and Japan. Natalie M. Gallant's co-authors include Sarah E. Millar, Thomas Andl, Yuhang Zhang, Stefano Piccolo, Ruth Schmidt‐Ullrich, Edward E. Morrisey, Steven Yang, Andrzej A. Dlugosz, Makoto M. Taketo and Fei Liu and has published in prestigious journals such as Nature Genetics, Developmental Cell and Developmental Biology.

In The Last Decade

Natalie M. Gallant

18 papers receiving 908 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Natalie M. Gallant United States 12 652 174 149 122 110 18 922
M Larrègue France 15 252 0.4× 48 0.3× 173 1.2× 49 0.4× 12 0.1× 117 736
Gabriele Mues United States 20 697 1.1× 29 0.2× 274 1.8× 107 0.9× 329 3.0× 32 949
Franco Crovato Italy 15 299 0.5× 67 0.4× 125 0.8× 73 0.6× 7 0.1× 56 772
Michael Michalec United States 6 401 0.6× 39 0.2× 47 0.3× 113 0.9× 36 0.3× 9 770
Miki Tanioka Japan 17 235 0.4× 29 0.2× 60 0.4× 62 0.5× 15 0.1× 53 858
Diana García‐Cruz Mexico 16 272 0.4× 65 0.4× 356 2.4× 42 0.3× 13 0.1× 81 727
Claire E. L. Smith United Kingdom 14 614 0.9× 150 0.9× 174 1.2× 474 3.9× 79 0.7× 25 835
Jon Williams United States 12 407 0.6× 84 0.5× 70 0.5× 146 1.2× 4 0.0× 20 1.1k
Shigeo Yamachika Japan 13 137 0.2× 9 0.1× 218 1.5× 108 0.9× 52 0.5× 27 766
H. Schell Germany 13 154 0.2× 174 1.0× 34 0.2× 40 0.3× 29 0.3× 72 615

Countries citing papers authored by Natalie M. Gallant

Since Specialization
Citations

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

Fields of papers citing papers by Natalie M. Gallant

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Natalie M. Gallant. 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 Natalie M. Gallant. The network helps show where Natalie M. Gallant may publish in the future.

Co-authorship network of co-authors of Natalie M. Gallant

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

All Works

18 of 18 papers shown
1.
Murali, Chaya N., John R. Barber, Robert McCarter, et al.. (2023). Health-related quality of life in a systematically assessed cohort of children and adults with urea cycle disorders. Molecular Genetics and Metabolism. 140(3). 107696–107696. 4 indexed citations
2.
Gallant, Stephanie, Diane Cassidy, Yan Hui Giam, et al.. (2021). The Protective Effect of SARS-CoV-2 Antibodies in Scottish Healthcare Workers. SSRN Electronic Journal. 3 indexed citations
3.
Gallant, Stephanie, Diane Cassidy, Yan Hui Giam, et al.. (2021). The protective effect of SARS-CoV-2 antibodies in Scottish healthcare workers. ERJ Open Research. 7(2). 80–2021. 19 indexed citations
4.
Haanpää, Maria K., Bobby G. Ng, Natalie M. Gallant, et al.. (2019). ALG11‐CDG syndrome: Expanding the phenotype. American Journal of Medical Genetics Part A. 179(3). 498–502. 12 indexed citations
5.
Powis, Zöe, Kelly D. Farwell Hagman, Kirsten Blanco, et al.. (2019). When moments matter: Finding answers with rapid exome sequencing. Molecular Genetics & Genomic Medicine. 8(2). e1027–e1027. 9 indexed citations
6.
Casillas, Jacqueline, Maki Okada, James B. Gibson, et al.. (2019). Hyperammonemia From Ureaplasma Infection in an Immunocompromised Child. Journal of Pediatric Hematology/Oncology. 42(2). e114–e116. 12 indexed citations
7.
Gallant, Natalie M., et al.. (2018). Neurofibromatosis type 1: a case highlighting pulmonary and other rare clinical manifestations. BMJ Case Reports. 2018. bcr–2017. 3 indexed citations
8.
Mullegama, Sureni V., Steven D. Klein, T. Niroshini Senaratne, et al.. (2017). De novo loss‐of‐function variants in STAG2 are associated with developmental delay, microcephaly, and congenital anomalies. American Journal of Medical Genetics Part A. 173(5). 1319–1327. 36 indexed citations
9.
Gallant, Natalie M., Yael Wilnai, Fred Lorey, et al.. (2017). Biochemical characteristics of newborns with carnitine transporter defect identified by newborn screening in California. Molecular Genetics and Metabolism. 122(3). 76–84. 20 indexed citations
10.
Wong, Derek A., Silvia Tortorelli, L.A. Bishop, et al.. (2015). Outcomes of four patients with homocysteine remethylation disorders detected by newborn screening. Genetics in Medicine. 18(2). 162–167. 21 indexed citations
11.
Gallant, Natalie M., Dorina Gui, Charles Lassman, et al.. (2014). Novel liver findings in Ornithine Transcarbamylase Deficiency due to Xp11.4-p21.1 microdeletion. Gene. 556(2). 249–253. 4 indexed citations
12.
Cederbaum, Stephen D., Julie Neidich, Natalie M. Gallant, et al.. (2013). Analysis of cases of 3-methylcrotonyl CoA carboxylase deficiency (3-MCCD) in the California newborn screening program reported in the state database. Molecular Genetics and Metabolism. 110(4). 477–483. 18 indexed citations
13.
Fan, Yuxin, Iris L. Gonzalez, Wim Kulik, et al.. (2013). A Novel Exonic Splicing Mutation in the TAZ (G4.5) Gene in a Case with Atypical Barth Syndrome. JIMD Reports. 11. 99–106. 4 indexed citations
14.
Gallant, Natalie M., Hao Tang, Lisa Feuchtbaum, et al.. (2012). Biochemical, molecular, and clinical characteristics of children with short chain acyl-CoA dehydrogenase deficiency detected by newborn screening in California. Molecular Genetics and Metabolism. 106(1). 55–61. 44 indexed citations
15.
Gallant, Natalie M., et al.. (2011). Pontocerebellar hypoplasia in association with de novo 19p13.11p13.12 microdeletion. American Journal of Medical Genetics Part A. 155(11). 2871–2878. 15 indexed citations
16.
Zhang, Yuhang, Thomas Andl, Natalie M. Gallant, et al.. (2009). Reciprocal Requirements for EDA/EDAR/NF-κB and Wnt/β-Catenin Signaling Pathways in Hair Follicle Induction. Developmental Cell. 17(1). 49–61. 269 indexed citations
17.
Liu, Fei, Emily Y. Chu, Brenda Watt, et al.. (2007). Wnt/β-catenin signaling directs multiple stages of tooth morphogenesis. Developmental Biology. 313(1). 210–224. 306 indexed citations
18.
Liu, Fei, Shoba Thirumangalathu, Natalie M. Gallant, et al.. (2006). Wnt-β-catenin signaling initiates taste papilla development. Nature Genetics. 39(1). 106–112. 123 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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