Heidi Dorward

3.0k total citations
27 papers, 1.9k citations indexed

About

Heidi Dorward is a scholar working on Molecular Biology, Cell Biology and Immunology. According to data from OpenAlex, Heidi Dorward has authored 27 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 9 papers in Cell Biology and 6 papers in Immunology. Recurrent topics in Heidi Dorward's work include melanin and skin pigmentation (8 papers), Research in Cotton Cultivation (3 papers) and Mitochondrial Function and Pathology (3 papers). Heidi Dorward is often cited by papers focused on melanin and skin pigmentation (8 papers), Research in Cotton Cultivation (3 papers) and Mitochondrial Function and Pathology (3 papers). Heidi Dorward collaborates with scholars based in United States, Israel and Sweden. Heidi Dorward's co-authors include Constantine Londos, Carole Sztalryd, Guoheng Xu, John T. Tansey, Alan R. Kimmel, Lyn Gold, Zhi‐Bin Tong, Lawrence M. Nelson, Carolyn A. Bondy and Juan Antonio Rojas‐Contreras and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and The Journal of Cell Biology.

In The Last Decade

Heidi Dorward

27 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Heidi Dorward United States 17 954 665 468 373 365 27 1.9k
Shoichiro Ikuyama Japan 27 796 0.8× 260 0.4× 272 0.6× 47 0.1× 111 0.3× 66 1.9k
Jeffrey B. Cheng United States 15 779 0.8× 140 0.2× 171 0.4× 89 0.2× 83 0.2× 32 1.9k
Seiko Masuda Japan 22 726 0.8× 178 0.3× 194 0.4× 100 0.3× 166 0.5× 25 1.5k
Katsuhiko Yasuda Japan 19 875 0.9× 117 0.2× 170 0.4× 172 0.5× 347 1.0× 48 1.6k
Indranil Sinha Sweden 24 1.2k 1.3× 64 0.1× 186 0.4× 56 0.2× 276 0.8× 47 1.8k
Christiane Ody France 21 808 0.8× 73 0.1× 211 0.5× 206 0.6× 145 0.4× 30 1.8k
Benny Chang United States 17 781 0.8× 374 0.6× 452 1.0× 20 0.1× 212 0.6× 23 1.6k
Yasuyuki Kitaura Japan 24 1.2k 1.2× 68 0.1× 402 0.9× 56 0.2× 402 1.1× 62 2.0k
Biao Lü United States 23 1.2k 1.3× 191 0.3× 167 0.4× 32 0.1× 117 0.3× 58 1.7k
Katrin Düvel United States 9 1.9k 2.0× 142 0.2× 385 0.8× 26 0.1× 359 1.0× 12 2.7k

Countries citing papers authored by Heidi Dorward

Since Specialization
Citations

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

Fields of papers citing papers by Heidi Dorward

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Heidi Dorward

This figure shows the co-authorship network connecting the top 25 collaborators of Heidi Dorward. A scholar is included among the top collaborators of Heidi Dorward 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 Heidi Dorward. Heidi Dorward 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.
Morimoto, Marie, Elena‐Raluca Nicoli, Joshi Stephen, et al.. (2023). cDNA sequencing increases the molecular diagnostic yield in Chediak-Higashi syndrome. Frontiers in Genetics. 14. 2 indexed citations
2.
Yokoyama, Tadafumi, Nathanial J. Tolman, Lauren Testa, et al.. (2022). Progressive pulmonary fibrosis in a murine model of Hermansky-Pudlak syndrome. Respiratory Research. 23(1). 112–112. 5 indexed citations
3.
Roney, Joseph C., Pedro Leuschner, Konrad Krzewski, et al.. (2020). Diagnosis of Chediak Higashi disease in a 67‐year old woman. American Journal of Medical Genetics Part A. 182(12). 3007–3013. 6 indexed citations
4.
Ikawa, Yasuhiro, Richard A. Hess, Heidi Dorward, et al.. (2014). In vitro functional correction of Hermansky–Pudlak Syndrome type-1 by lentiviral-mediated gene transfer. Molecular Genetics and Metabolism. 114(1). 62–65. 12 indexed citations
5.
Lam, Christina, Carla Ciccone, Heidi Dorward, et al.. (2014). Two novel compound heterozygous mutations in OPA3 in two siblings with OPA3-related 3-methylglutaconic aciduria. Molecular Genetics and Metabolism Reports. 1. 114–123. 6 indexed citations
6.
Leoyklang, Petcharat, Kanya Suphapeetiporn, Chalurmpon Srichomthong, et al.. (2013). Disorders with similar clinical phenotypes reveal underlying genetic interaction: SATB2 acts as an activator of the UPF3B gene. Human Genetics. 132(12). 1383–1393. 24 indexed citations
7.
Cullinane, Andrew R., Heidi Dorward, Carmelo Carmona‐Rivera, et al.. (2013). Dysregulation of Galectin-3. Implications for Hermansky-Pudlak Syndrome Pulmonary Fibrosis. American Journal of Respiratory Cell and Molecular Biology. 50(3). 605–613. 38 indexed citations
8.
Markello, Thomas C., Cynthia St. Hilaire, Heidi Dorward, et al.. (2011). Vascular pathology of medial arterial calcifications in NT5E deficiency: Implications for the role of adenosine in pseudoxanthoma elasticum. Molecular Genetics and Metabolism. 103(1). 44–50. 88 indexed citations
9.
Westbroek, Wendy, Aharon Klar, Andrew R. Cullinane, et al.. (2011). Cellular and clinical report of new Griscelli syndrome type III cases. Pigment Cell & Melanoma Research. 25(1). 47–56. 22 indexed citations
10.
Vincent, Lisa M., Fiona J. Gilbert, Jennifer DiPace, et al.. (2010). Novel 47.5-kb deletion in RAB27A results in severe Griscelli Syndrome Type 2. Molecular Genetics and Metabolism. 101(1). 62–65. 11 indexed citations
11.
Huizing, Marjan, Heidi Dorward, Enriko Klootwijk, et al.. (2010). OPA3, mutated in 3-methylglutaconic aciduria type III, encodes two transcripts targeted primarily to mitochondria. Molecular Genetics and Metabolism. 100(2). 149–154. 20 indexed citations
12.
Wang, Hong, Liping Hu, Knut Tomas Dalen, et al.. (2009). Activation of Hormone-sensitive Lipase Requires Two Steps, Protein Phosphorylation and Binding to the PAT-1 Domain of Lipid Droplet Coat Proteins. Journal of Biological Chemistry. 284(46). 32116–32125. 139 indexed citations
13.
Huizing, Marjan, Richard A. Hess, Allison Griffin, et al.. (2009). Clinical and cellular characterisation of Hermansky–Pudlak syndrome type 6. Journal of Medical Genetics. 46(12). 803–810. 41 indexed citations
14.
Helip‐Wooley, Amanda, Wendy Westbroek, Heidi Dorward, et al.. (2007). Improper Trafficking of Melanocyte-Specific Proteins in Hermansky–Pudlak Syndrome Type-5. Journal of Investigative Dermatology. 127(6). 1471–1478. 34 indexed citations
15.
Sparks, Susan, Goran Rakočević, Galen O. Joe, et al.. (2007). Intravenous immune globulin in hereditary inclusion body myopathy: a pilot study. BMC Neurology. 7(1). 3–3. 44 indexed citations
16.
Helip‐Wooley, Amanda, Wendy Westbroek, Heidi Dorward, et al.. (2005). Association of the Hermansky-Pudlak syndrome type-3 protein with clathrin. BMC Cell Biology. 6(1). 33–33. 15 indexed citations
17.
Xu, Guoheng, Carole Sztalryd, Xinyue Lu, et al.. (2005). Post-translational Regulation of Adipose Differentiation-related Protein by the Ubiquitin/Proteasome Pathway. Journal of Biological Chemistry. 280(52). 42841–42847. 224 indexed citations
18.
Huizing, Marjan, Richard A. Hess, Heidi Dorward, et al.. (2004). Cellular, Molecular and Clinical Characterization of Patients with Hermansky–Pudlak Syndrome Type 5. Traffic. 5(9). 711–722. 54 indexed citations
19.
Tong, Zhi‐Bin, Lyn Gold, Anto De Pol, et al.. (2003). Developmental Expression and Subcellular Localization of Mouse MATER, an Oocyte-Specific Protein Essential for Early Development. Endocrinology. 145(3). 1427–1434. 79 indexed citations
20.
Tong, Zhi‐Bin, Lyn Gold, Karl Pfeifer, et al.. (2000). Mater, a maternal effect gene required for early embryonic development in mice. Nature Genetics. 26(3). 267–268. 447 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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