Katrina Haude

1.1k total citations
6 papers, 118 citations indexed

About

Katrina Haude is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Endocrine and Autonomic Systems. According to data from OpenAlex, Katrina Haude has authored 6 papers receiving a total of 118 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 1 paper in Pediatrics, Perinatology and Child Health and 1 paper in Endocrine and Autonomic Systems. Recurrent topics in Katrina Haude's work include Mitochondrial Function and Pathology (2 papers), ATP Synthase and ATPases Research (2 papers) and Genomics and Rare Diseases (1 paper). Katrina Haude is often cited by papers focused on Mitochondrial Function and Pathology (2 papers), ATP Synthase and ATPases Research (2 papers) and Genomics and Rare Diseases (1 paper). Katrina Haude collaborates with scholars based in United States, China and Canada. Katrina Haude's co-authors include Heather Zierhut, Bonnie S. LeRoy, Patricia McCarthy Veach, Jeffrey W. Innis, Linshan Shang, Wendy K. Chung, Hong Cui, Jonathan Picker, Megan T. Cho and Mark A. Tarnopolsky and has published in prestigious journals such as Human Molecular Genetics, Human Mutation and Neurogenetics.

In The Last Decade

Katrina Haude

5 papers receiving 117 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Katrina Haude United States	5	81	41	24	15	10	6	118
Chontelle King New Zealand	6	48 0.6×	51 1.2×	9 0.4×	12 0.8×	10 1.0×	6	109
Leigh Demain United Kingdom	7	134 1.7×	48 1.2×	35 1.5×	12 0.8×	24 2.4×	12	209
Fathiya Al Murshedi Oman	6	45 0.6×	56 1.4×	12 0.5×	10 0.7×	8 0.8×	14	114
Nurit Assia Batzir Israel	5	58 0.7×	43 1.0×	12 0.5×	6 0.4×	11 1.1×	9	92
Ali Abdullah Alfaiz Switzerland	5	108 1.3×	33 0.8×	13 0.5×	18 1.2×	6 0.6×	6	138
Stephanie Karch Germany	8	101 1.2×	50 1.2×	14 0.6×	5 0.3×	11 1.1×	8	146
Sonal Mahida United States	8	93 1.1×	124 3.0×	18 0.8×	12 0.8×	19 1.9×	13	210
Jessica Sebastian United States	6	64 0.8×	92 2.2×	5 0.2×	9 0.6×	21 2.1×	11	146
Marion I. Stunault United States	5	59 0.7×	17 0.4×	7 0.3×	9 0.6×	11 1.1×	8	145
Muhsin Elmas Türkiye	6	47 0.6×	32 0.8×	9 0.4×	11 0.7×	10 1.0×	25	89

Countries citing papers authored by Katrina Haude

Since Specialization

Citations

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

Fields of papers citing papers by Katrina Haude

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katrina Haude

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

All Works

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6 of 6 papers shown

1.

Slone, Jesse, Katrina Haude, Hong Cui, et al.. (2020). Mitochondrial genome variant m.3250T>C as a possible risk factor for mitochondrial cardiomyopathy. Human Mutation. 42(2). 177–188. 7 indexed citations

2.

Lam, Christina, Hong Cui, Katrina Haude, et al.. (2018). Aberrant Drp1-mediated mitochondrial division presents in humans with variable outcomes. Human Molecular Genetics. 27(21). 3710–3719. 38 indexed citations

3.

Haude, Katrina, Patricia McCarthy Veach, Bonnie S. LeRoy, & Heather Zierhut. (2016). Factors Influencing the Decision‐Making Process and Long‐Term Interpersonal Outcomes for Parents Who Undergo Preimplantation Genetic Diagnosis for Fanconi Anemia: a Qualitative Investigation. Journal of Genetic Counseling. 26(3). 640–655. 15 indexed citations

4.

Shang, Linshan, Lindsay B. Henderson, Megan T. Cho, et al.. (2015). De novo missense variants in PPP2R5D are associated with intellectual disability, macrocephaly, hypotonia, and autism. Neurogenetics. 17(1). 43–49. 52 indexed citations

5.

Wittlieb‐Weber, Carol, Katrina Haude, Chin‐To Fong, & Jeffrey M. Vinocur. (2015). A novel GJA1 mutation causing familial oculodentodigital dysplasia with dilated cardiomyopathy and arrhythmia. HeartRhythm Case Reports. 2(1). 32–35. 6 indexed citations

6.

Haude, Katrina, et al.. (2013). Analyzing the Role of Receptor Internalization in the Regulation of Melanin-Concentrating Hormone Signaling. International Journal of Endocrinology. 2013. 1–10.

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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