Helen Lord

605 total citations
9 papers, 128 citations indexed

About

Helen Lord is a scholar working on Genetics, Molecular Biology and Social Psychology. According to data from OpenAlex, Helen Lord has authored 9 papers receiving a total of 128 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 1 paper in Social Psychology. Recurrent topics in Helen Lord's work include Craniofacial Disorders and Treatments (5 papers), Cleft Lip and Palate Research (4 papers) and Connective tissue disorders research (2 papers). Helen Lord is often cited by papers focused on Craniofacial Disorders and Treatments (5 papers), Cleft Lip and Palate Research (4 papers) and Connective tissue disorders research (2 papers). Helen Lord collaborates with scholars based in United Kingdom, United States and Netherlands. Helen Lord's co-authors include Tracy Lester, Andrew O.M. Wilkie, Jasmine Lim, David Johnson, Anne Goriely, Helen V. Firth, Steven A. Wall, Vikram Sharma, Konstantinos Varvagiannis and Michael B. Petersen and has published in prestigious journals such as Human Molecular Genetics, Journal of Medical Genetics and European Journal of Human Genetics.

In The Last Decade

Helen Lord

9 papers receiving 116 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Helen Lord United Kingdom	7	93	67	17	13	9	9	128
Paul R. Mark United States	7	58 0.6×	70 1.0×	14 0.8×	8 0.6×	9 1.0×	11	123
Christel Thauvin-Robinet France	6	69 0.7×	65 1.0×	26 1.5×	16 1.2×	6 0.7×	7	124
Federica Tamburrino Italy	9	80 0.9×	102 1.5×	13 0.8×	15 1.2×	13 1.4×	16	174
Margaret Harr United States	10	130 1.4×	79 1.2×	29 1.7×	18 1.4×	13 1.4×	16	194
Ricarda Flöttmann Germany	8	95 1.0×	111 1.7×	19 1.1×	7 0.5×	13 1.4×	12	163
Troy J. Gliem United States	5	66 0.7×	67 1.0×	20 1.2×	12 0.9×	12 1.3×	11	102
Kévin Yauy France	6	72 0.8×	56 0.8×	20 1.2×	7 0.5×	10 1.1×	12	114
Gaëlle Vieville France	6	86 0.9×	63 0.9×	18 1.1×	11 0.8×	5 0.6×	9	127
Catrina M. Loucks Canada	6	36 0.4×	64 1.0×	8 0.5×	5 0.4×	10 1.1×	18	113
Jonathan Marquez United States	10	56 0.6×	139 2.1×	8 0.5×	12 0.9×	11 1.2×	16	174

Countries citing papers authored by Helen Lord

Since Specialization

Citations

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

Fields of papers citing papers by Helen Lord

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Helen Lord

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

All Works

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9 of 9 papers shown

Luyckx, Ilse, Nele Boeckx, Kristof Van Schil, et al.. (2024). Homozygous SMAD6 variants in two unrelated patients with craniosynostosis and radioulnar synostosis. Journal of Medical Genetics. 61(4). 363–368. 2 indexed citations

Lord, Helen, et al.. (2020). Exploring health and social care professionals’ initial perceptions of caring for trans patients. Nursing Standard. 35(10). 44–49. 3 indexed citations

Calder, Alistair, Tracy Lester, Helen Lord, et al.. (2018). A three-generation family with metaphyseal dysplasia, maxillary hypoplasia and brachydactyly (MDMHB) due to intragenic RUNX2 duplication. European Journal of Human Genetics. 26(9). 1288–1293. 9 indexed citations

Kim, Sharon, Stephen R.F. Twigg, Aditi Chandra, et al.. (2017). Localized TWIST1 and TWIST2 basic domain substitutions cause four distinct human diseases that can be modeled in Caenorhabditis elegans. Human Molecular Genetics. 26(11). 2118–2132. 18 indexed citations

Balasubramanian, Meena, Helen Lord, Sébastien Levesque, et al.. (2016). Chitayat syndrome: hyperphalangism, characteristic facies, hallux valgus and bronchomalacia results from a recurrent c.266A>G p.(Tyr89Cys) variant in the ERF gene. Journal of Medical Genetics. 54(3). 157–165. 15 indexed citations

Fenwick, Aimée L, Jacqueline A.C. Goos, Julia Rankin, et al.. (2014). Apparently synonymous substitutions in FGFR2affect splicing and result in mild Crouzon syndrome. BMC Medical Genetics. 15(1). 95–95. 12 indexed citations

Varvagiannis, Konstantinos, Yolanda Gyftodimou, Helen Lord, et al.. (2013). Pure de novo partial trisomy 6p in a girl with craniosynostosis. American Journal of Medical Genetics Part A. 161(2). 343–351. 28 indexed citations

Sharma, Vikram, Steven A. Wall, Helen Lord, Tracy Lester, & Andrew O.M. Wilkie. (2011). Atypical Crouzon Syndrome with a Novel Cys62Arg Mutation in FGFR2 Presenting with Sagittal Synostosis. The Cleft Palate-Craniofacial Journal. 49(3). 373–377. 15 indexed citations

Goriely, Anne, Helen Lord, Jasmine Lim, et al.. (2010). Germline and somatic mosaicism for FGFR2 mutation in the mother of a child with Crouzon syndrome: Implications for genetic testing in “paternal age‐effect” syndromes. American Journal of Medical Genetics Part A. 152A(8). 2067–2073. 26 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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