Sandra Barral

9.5k total citations
13 papers, 399 citations indexed

About

Sandra Barral is a scholar working on Genetics, Molecular Biology and Ophthalmology. According to data from OpenAlex, Sandra Barral has authored 13 papers receiving a total of 399 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Ophthalmology. Recurrent topics in Sandra Barral's work include Genetic Associations and Epidemiology (5 papers), Retinal Diseases and Treatments (3 papers) and Genomics and Rare Diseases (2 papers). Sandra Barral is often cited by papers focused on Genetic Associations and Epidemiology (5 papers), Retinal Diseases and Treatments (3 papers) and Genomics and Rare Diseases (2 papers). Sandra Barral collaborates with scholars based in United States, Spain and Netherlands. Sandra Barral's co-authors include Joseph H. Lee, Christiane Reitz, Richard Mayeux, Rafael Lantigua, Rong Cheng, Martin Medrano, Peter St George‐Hyslop, Ekaterina Rogaeva, Ivonne Z. Jiménez‐Velázquez and A Kahn and has published in prestigious journals such as Annals of Neurology, Diabetologia and American Journal of Ophthalmology.

In The Last Decade

Sandra Barral

12 papers receiving 395 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sandra Barral United States	8	208	185	102	44	40	13	399
Elizabeth Snella United States	13	177 0.9×	120 0.6×	49 0.5×	42 1.0×	18 0.5×	25	429
Foudil Lamari France	14	227 1.1×	257 1.4×	58 0.6×	80 1.8×	59 1.5×	28	582
Linghan Gao China	13	41 0.2×	277 1.5×	120 1.2×	51 1.2×	31 0.8×	23	462
Purnima P. Desai United States	8	139 0.7×	126 0.7×	41 0.4×	73 1.7×	27 0.7×	8	349
P. Borboni Italy	15	114 0.5×	327 1.8×	62 0.6×	87 2.0×	7 0.2×	28	659
I Klisak United States	13	80 0.4×	405 2.2×	124 1.2×	59 1.3×	26 0.7×	19	682
Susana Carmona Portugal	7	172 0.8×	133 0.7×	38 0.4×	69 1.6×	39 1.0×	18	387
Nina Schultz Sweden	12	169 0.8×	84 0.5×	20 0.2×	44 1.0×	44 1.1×	18	346
Pierre Chryso Djoufack Germany	5	64 0.3×	115 0.6×	32 0.3×	69 1.6×	12 0.3×	7	336
Grzeschik Kh Germany	6	107 0.5×	166 0.9×	52 0.5×	26 0.6×	10 0.3×	9	268

Countries citing papers authored by Sandra Barral

Since Specialization

Citations

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

Fields of papers citing papers by Sandra Barral

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sandra Barral

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

All Works

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13 of 13 papers shown

Nafikov, Rafael A., Alejandro Q. Nato, Harkirat Sohi, et al.. (2018). Analysis of pedigree data in populations with multiple ancestries: Strategies for dealing with admixture in Caribbean Hispanic families from the ADSP. Genetic Epidemiology. 42(6). 500–515. 3 indexed citations

Beecham, Gary W., Badri N. Vardarajan, Elizabeth Blue, et al.. (2017). [O2–08–03]: WHOLE‐GENOME SEQUENCING IN FAMILIAL LATE‐ONSET ALZHEIMER's DISEASE IDENTIFIES RARE VARIATION IN AD CANDIDATE GENES. Alzheimer s & Dementia. 13(7S_Part_11).

Jakkula, Eveliina, Olli‐Pekka Kämäräinen, Ping Gao, et al.. (2015). Targeted re-sequencing of linkage region on 2q21 identifies a novel functional variant for hip and knee osteoarthritis. Osteoarthritis and Cartilage. 24(4). 655–663. 8 indexed citations

Vardarajan, Badri N., Mahdi Ghani, A Kahn, et al.. (2015). Rare coding mutations identified by sequencing of Alzheimer disease genome‐wide association studies loci. Annals of Neurology. 78(3). 487–498. 110 indexed citations

Barral, Sandra, Israel Fernández‐Cadenas, Joshua C. Bis, et al.. (2011). No association of ALOX5AP polymorphisms with risk of MRI-defined brain infarcts. Neurobiology of Aging. 33(3). 629.e1–629.e3. 7 indexed citations

Lee, Joseph H., Rong Cheng, Sandra Barral, et al.. (2010). Identification of Novel Loci for Alzheimer Disease and Replication of CLU, PICALM, and BIN1 in Caribbean Hispanic Individuals. Archives of Neurology. 68(3). 320–8. 141 indexed citations

Lee, Joseph H., Sandra Barral, & Christiane Reitz. (2008). The neuronal sortilin-related receptor gene SORL1 and late-onset Alzheimer’s disease. Current Neurology and Neuroscience Reports. 8(5). 384–391. 39 indexed citations

Kaňková, Kateřina, Lukáš Pácal, Lýdie Izakovičová Hollá, et al.. (2007). Genetic risk factors for diabetic nephropathy on chromosomes 6p and 7q identified by the set-association approach. Diabetologia. 50(5). 990–999. 24 indexed citations

Barral, Sandra, Peter J. Francis, David Schultz, et al.. (2007). Expanded genome scan in extended families with age-related macular degeneration. American Journal of Ophthalmology. 143(2). 376–376. 1 indexed citations

10.

Barral, Sandra, Peter J. Francis, Dennis W. Schultz, et al.. (2006). Expanded Genome Scan in Extended Families with Age-Related Macular Degeneration. Investigative Ophthalmology & Visual Science. 47(12). 5453–5453. 14 indexed citations

11.

Barral, Sandra, Chad Haynes, Mark A. Levenstien, & Derek Gordon. (2005). Precision and type I error rate in the presence of genotype errors and missing parental data: a comparison between the original transmission disequilibrium test (TDT) and TDTae statistics. BMC Genetics. 6(S1). S150–S150. 11 indexed citations

12.

Schultz, Dennis W., Richard G. Weleber, Sandra Barral, et al.. (2005). HEMICENTIN-1 (FIBULIN-6) and the 1q31 AMD Locus in the Context of Complex Disease: Review and Perspective. Ophthalmic Genetics. 26(2). 101–105. 37 indexed citations

13.

Barral, Sandra, M.V. Lareu, Antonio Salas, & Ãngel Carracedo. (2000). Sequence variation of two hypervariable short tandem repeats at the D22S683 and D6S477 loci. International Journal of Legal Medicine. 113(3). 146–149. 4 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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