Melanie Patterson

766 total citations
6 papers, 61 citations indexed

About

Melanie Patterson is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Melanie Patterson has authored 6 papers receiving a total of 61 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Clinical Biochemistry and 2 papers in Genetics. Recurrent topics in Melanie Patterson's work include Mitochondrial Function and Pathology (2 papers), Genomics and Rare Diseases (1 paper) and Bacterial Identification and Susceptibility Testing (1 paper). Melanie Patterson is often cited by papers focused on Mitochondrial Function and Pathology (2 papers), Genomics and Rare Diseases (1 paper) and Bacterial Identification and Susceptibility Testing (1 paper). Melanie Patterson collaborates with scholars based in United States, Japan and Germany. Melanie Patterson's co-authors include Carol Saunders, Laurie D. Smith, Emily Farrow, Neil Miller, Margaret Gibson, Isabelle Thiffault, Chengpeng Bi, Stephen F. Kingsmore, Weiwei Zhao and Eugenio Taboada and has published in prestigious journals such as Human Mutation, American Journal of Medical Genetics Part A and Journal of Pediatric Hematology/Oncology.

In The Last Decade

Melanie Patterson

5 papers receiving 61 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Melanie Patterson United States	4	46	19	16	13	6	6	61
Jullianne Diaz United States	6	62 1.3×	28 1.5×	13 0.8×	18 1.4×	2 0.3×	10	89
Abdullah Alfaifi Saudi Arabia	3	41 0.9×	23 1.2×	13 0.8×	6 0.5×	4 0.7×	4	66
Yanshuang Zhou China	4	87 1.9×	12 0.6×	12 0.8×	11 0.8×	4 0.7×	7	124
Richa Khanna India	6	72 1.6×	8 0.4×	16 1.0×	4 0.3×	4 0.7×	7	105
Rocío Nieto-Arellano Spain	4	112 2.4×	13 0.7×	17 1.1×	16 1.2×		4	134
Anna Kabala Poland	4	98 2.1×	6 0.3×	6 0.4×	23 1.8×	5 0.8×	4	116
Jan-Ulrich Schlump Germany	4	31 0.7×	25 1.3×	3 0.2×	30 2.3×	20 3.3×	4	77
Dyala Jaroudi Saudi Arabia	3	49 1.1×	12 0.6×	9 0.6×	5 0.4×		3	62
Junpu Mei China	7	38 0.8×	12 0.6×	5 0.3×	6 0.5×	3 0.5×	13	91
Colby T. Marvin United States	3	32 0.7×	26 1.4×	15 0.9×	3 0.2×		3	51

Countries citing papers authored by Melanie Patterson

Since Specialization

Citations

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

Fields of papers citing papers by Melanie Patterson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Melanie Patterson

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

All Works

Sort: Min cites: Since: Top N: Style:

6 of 6 papers shown

1.

Amudhavalli, Shivarajan, Melanie Patterson, Jennifer Kussmann, et al.. (2023). Novel blended SNRPE‐related spliceosomopathy phenotype characterized by microcephaly and congenital atrichia. American Journal of Medical Genetics Part A. 191(5). 1425–1429.

2.

Mizumoto, Shuji, Laurie D. Smith, Howard M. Saal, et al.. (2016). Functional validation of novel compound heterozygous variants in B3GAT3 resulting in severe osteopenia and fractures: expanding the disease phenotype. BMC Medical Genetics. 17(1). 86–86. 16 indexed citations

3.

Saunders, Carol, Sung Ho Moon, Xinping Liu, et al.. (2015). Loss of Function Variants in HumanPNPLA8Encoding Calcium-Independent Phospholipase A₂γ Recapitulate the Mitochondriopathy of the Homologous Null Mouse. Human Mutation. 36(6). 656–656. 1 indexed citations

4.

Saunders, Carol, Sung Ho Moon, Xinping Liu, et al.. (2014). Loss of Function Variants in Human PNPLA8 Encoding Calcium-Independent Phospholipase A₂γ Recapitulate the Mitochondriopathy of the Homologous Null Mouse. Human Mutation. 36(3). 301–306. 27 indexed citations

5.

Singh, Jasjit, et al.. (2013). Vancomycin-resistant Enterococcus in Pediatric Oncology Patients. Journal of Pediatric Hematology/Oncology. 35(3). 227–231. 7 indexed citations

6.

Saunders, Carol, et al.. (2010). Allele Drop-Out in the MECP2 Gene Due to G-Quadruplex and i-Motif Sequences When Using Polymerase Chain Reaction-Based Diagnosis for Rett Syndrome. Genetic Testing and Molecular Biomarkers. 14(2). 241–247. 10 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