Sally Martell

450 total citations
12 papers, 289 citations indexed

About

Sally Martell is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sally Martell has authored 12 papers receiving a total of 289 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Sally Martell's work include Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genomics and Rare Diseases (3 papers). Sally Martell is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genomics and Rare Diseases (3 papers). Sally Martell collaborates with scholars based in Canada, United Kingdom and United States. Sally Martell's co-authors include Evica Rajcan‐Separovic, M. E. Suzanne Lewis, Ying Qiao, Jiadi Wen, Mary D. Stephenson, Peter C. K. Leung, Ying Qiao, Wendy P. Robinson, Chieko Chijiwa and Monica Hrynchak and has published in prestigious journals such as Human Mutation, Molecular Human Reproduction and Orphanet Journal of Rare Diseases.

In The Last Decade

Sally Martell

12 papers receiving 264 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sally Martell Canada	10	178	131	83	48	24	12	289
M. Elizabeth McCready Canada	10	120 0.7×	80 0.6×	39 0.5×	25 0.5×	14 0.6×	25	254
Christine Tyson Canada	12	319 1.8×	143 1.1×	162 2.0×	50 1.0×	80 3.3×	14	435
Maria Paola Recalcati Italy	11	240 1.3×	191 1.5×	89 1.1×	22 0.5×	46 1.9×	21	378
Ioannis Papoulidis Greece	13	251 1.4×	116 0.9×	195 2.3×	13 0.3×	51 2.1×	52	388
Patricia Mowery‐Rushton United States	9	167 0.9×	109 0.8×	74 0.9×	19 0.4×	35 1.5×	13	242
Drew Duckett United Kingdom	9	249 1.4×	142 1.1×	128 1.5×	12 0.3×	63 2.6×	23	353
Ruslan Strogantsev United Kingdom	9	203 1.1×	361 2.8×	102 1.2×	24 0.5×	34 1.4×	10	420
William Fergusson United Kingdom	9	125 0.7×	97 0.7×	41 0.5×	67 1.4×	36 1.5×	14	255
Ghislain Auclair France	5	136 0.8×	395 3.0×	70 0.8×	15 0.3×	18 0.8×	6	445
Barbara Delle Chiaie Belgium	7	251 1.4×	195 1.5×	136 1.6×	22 0.5×	38 1.6×	10	423

Countries citing papers authored by Sally Martell

Since Specialization

Citations

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

Fields of papers citing papers by Sally Martell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sally Martell

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

All Works

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12 of 12 papers shown

Qiao, Ying, Brett Trost, Kristina Calli, et al.. (2022). Complex Autism Spectrum Disorder with Epilepsy, Strabismus and Self-Injurious Behaviors in a Patient with a De Novo Heterozygous POLR2A Variant. Genes. 13(3). 470–470. 5 indexed citations

Qiao, Ying, Kristina Calli, Sally Martell, et al.. (2021). Contribution of Multiple Inherited Variants to Autism Spectrum Disorder (ASD) in a Family with 3 Affected Siblings. Genes. 12(7). 1053–1053. 14 indexed citations

Qiao, Ying, Sally Martell, M. E. Suzanne Lewis, et al.. (2018). Exome sequencing identified a de novo mutation of PURA gene in a patient with familial Xp22.31 microduplication. European Journal of Medical Genetics. 62(2). 103–108. 16 indexed citations

Qiao, Ying, Sally Martell, M. E. Suzanne Lewis, et al.. (2017). Whole exome sequencing of families with 1q21.1 microdeletion or microduplication. American Journal of Medical Genetics Part A. 173(7). 1782–1791. 19 indexed citations

Qiao, Ying, Jiadi Wen, Sally Martell, et al.. (2016). Whole exome sequencing in recurrent early pregnancy loss. Molecular Human Reproduction. 22(5). 364–372. 69 indexed citations

Chijiwa, Chieko, et al.. (2016). Exome sequencing identifies pathogenic variants of VPS13B in a patient with familial 16p11.2 duplication. BMC Medical Genetics. 17(1). 78–78. 24 indexed citations

Qiao, Ying, Rita Colnaghi, Diana Alcantara, et al.. (2016). Identifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysis. JCI Insight. 1(3). e85461–e85461. 23 indexed citations

Wen, Jiadi, Courtney W. Hanna, Sally Martell, et al.. (2015). Functional consequences of copy number variants in miscarriage. Molecular Cytogenetics. 8(1). 6–6. 15 indexed citations

Qiao, Ying, Kajari Mondal, Valentina Trapani, et al.. (2013). Variant ATRX Syndrome with Dysfunction ofATRXandMAGT1Genes. Human Mutation. 35(1). 58–62. 8 indexed citations

10.

Wen, Jiadi, Fátima Lopes, Gabriela Soares, et al.. (2013). Phenotypic and functional consequences of haploinsufficiency of genes from exocyst and retinoic acid pathway due to a recurrent microdeletion of 2p13.2. Orphanet Journal of Rare Diseases. 8(1). 100–100. 21 indexed citations

11.

Qiao, Ying, Christine Tyson, Monica Hrynchak, et al.. (2012). Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disability. Clinical Genetics. 83(2). 145–154. 32 indexed citations

12.

Harvard, Chansonette, Eloi Mercier, Rita Colnaghi, et al.. (2011). Understanding the impact of 1q21.1 copy number variant. Orphanet Journal of Rare Diseases. 6(1). 54–54. 43 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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