Laura Addis

3.1k total citations
15 papers, 613 citations indexed

About

Laura Addis is a scholar working on Genetics, Molecular Biology and Developmental and Educational Psychology. According to data from OpenAlex, Laura Addis has authored 15 papers receiving a total of 613 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 5 papers in Molecular Biology and 4 papers in Developmental and Educational Psychology. Recurrent topics in Laura Addis's work include Genetics and Neurodevelopmental Disorders (9 papers), Language Development and Disorders (4 papers) and Genomics and Rare Diseases (3 papers). Laura Addis is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Language Development and Disorders (4 papers) and Genomics and Rare Diseases (3 papers). Laura Addis collaborates with scholars based in United Kingdom, Canada and United States. Laura Addis's co-authors include Anthony P. Monaco, Dianne F. Newbury, Deb K. Pal, Joel B. Talcott, John Stein, Silvia Paracchini, Tom S. Scerri, Laura Winchester, A.J. Richardson and Janet G. Walter and has published in prestigious journals such as Journal of Biological Chemistry, Bioinformatics and PLoS ONE.

In The Last Decade

Laura Addis

15 papers receiving 605 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Laura Addis United Kingdom	11	262	213	195	150	125	15	613
Glenda Lassi Italy	11	124 0.5×	82 0.4×	506 2.6×	153 1.0×	159 1.3×	19	851
Fahimeh Darki Sweden	10	119 0.5×	200 0.9×	334 1.7×	84 0.6×	59 0.5×	23	606
Ruth C. M. Philip United Kingdom	9	306 1.2×	149 0.7×	793 4.1×	95 0.6×	41 0.3×	9	911
Ohiko Hashimoto Japan	12	229 0.9×	44 0.2×	261 1.3×	158 1.1×	49 0.4×	28	659
Hans Berger Netherlands	16	42 0.2×	80 0.4×	317 1.6×	173 1.2×	34 0.3×	28	830
Laurence Robel France	16	243 0.9×	128 0.6×	456 2.3×	170 1.1×	39 0.3×	48	766
James Hodgson United States	4	257 1.0×	141 0.7×	562 2.9×	80 0.5×	27 0.2×	6	655
Nicholas S. Waters United States	14	65 0.2×	79 0.4×	326 1.7×	76 0.5×	16 0.1×	18	565
Jaana Nopola‐Hemmi Finland	13	564 2.2×	710 3.3×	204 1.0×	257 1.7×	20 0.2×	14	1.0k
I. Laurence MacPhie United Kingdom	12	562 2.1×	576 2.7×	575 2.9×	169 1.1×	57 0.5×	12	1.3k

Countries citing papers authored by Laura Addis

Since Specialization

Citations

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

Fields of papers citing papers by Laura Addis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura Addis

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

All Works

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15 of 15 papers shown

Addis, Laura, William Sproviero, Sanjeev V. Thomas, et al.. (2018). Identification of new risk factors for rolandic epilepsy: CNV at Xp22.31 and alterations at cholinergic synapses. Journal of Medical Genetics. 55(9). 607–616. 19 indexed citations

Addis, Laura, et al.. (2017). Epilepsy-associated GRIN2A mutations reduce NMDA receptor trafficking and agonist potency – molecular profiling and functional rescue. Scientific Reports. 7(1). 66–66. 73 indexed citations

Addis, Laura, Richard Rosch, Antonio Valentı́n, et al.. (2016). Analysis of rare copy number variation in absence epilepsies. Neurology Genetics. 2(2). e56–e56. 24 indexed citations

Derkach, Andriy, Theodore Chiang, Jiafen Gong, et al.. (2014). Association analysis using next-generation sequence data from publicly available control groups: the robust variance score statistic. Bioinformatics. 30(15). 2179–2188. 21 indexed citations

Simpson, Nuala H., Laura Addis, William M. Brandler, et al.. (2013). Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia. Developmental Medicine & Child Neurology. 56(4). 346–353. 27 indexed citations

Addis, Laura, Theodore Chiang, Tara Clarke, et al.. (2013). Evidence for linkage of migraine in Rolandic epilepsy to known 1q23 FHM2 and novel 17q22 genetic loci. Genes Brain & Behavior. 13(3). 333–340. 6 indexed citations

Addis, Laura, Jack J. Lin, Deb K. Pal, Bruce P. Hermann, & Rochelle Caplan. (2012). Imaging and genetics of language and cognition in pediatric epilepsy. Epilepsy & Behavior. 26(3). 303–312. 7 indexed citations

Strug, Lisa J., Laura Addis, Theodore Chiang, et al.. (2012). The Genetics of Reading Disability in an Often Excluded Sample: Novel Loci Suggested for Reading Disability in Rolandic Epilepsy. PLoS ONE. 7(7). e40696–e40696. 12 indexed citations

Addis, Laura, David Collier, & Deb K. Pal. (2012). EXPANDING THE ROLE OF COPY NUMBER VARIATION IN EPILEPSY PATHOLOGY. 53. 42–42. 1 indexed citations

10.

Addis, Laura, Angela D. Friederici, Sonja A. Kotz, et al.. (2010). A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31‐q14.3. Genes Brain & Behavior. 9(6). 545–561. 23 indexed citations

11.

Haglund, Lisbet, Viveka Tillgren, Laura Addis, et al.. (2010). Identification and Characterization of the Integrin α2β1 Binding Motif in Chondroadherin Mediating Cell Attachment. Journal of Biological Chemistry. 286(5). 3925–3934. 28 indexed citations

12.

Newbury, Dianne F., Silvia Paracchini, Tom S. Scerri, et al.. (2010). Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects. Behavior Genetics. 41(1). 90–104. 162 indexed citations

13.

Asher, Julian E., Janine A. Lamb, Denise Brocklebank, et al.. (2009). A Whole-Genome Scan and Fine-Mapping Linkage Study of Auditory-Visual Synesthesia Reveals Evidence of Linkage to Chromosomes 2q24, 5q33, 6p12, and 12p12. The American Journal of Human Genetics. 84(2). 279–285. 138 indexed citations

14.

Addis, Laura, et al.. (2008). Purification, crystallization and preliminary X-ray diffraction analysis of human chondroadherin. Acta Crystallographica Section F Structural Biology and Crystallization Communications. 64(6). 516–519. 1 indexed citations

15.

Falcaro, Milena, Andrew Pickles, Dianne F. Newbury, et al.. (2007). Genetic and phenotypic effects of phonological short‐term memory and grammatical morphology in specific language impairment. Genes Brain & Behavior. 7(4). 393–402. 71 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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