Melissa T. Carter

5.3k total citations
34 papers, 616 citations indexed

About

Melissa T. Carter is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Melissa T. Carter has authored 34 papers receiving a total of 616 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 20 papers in Molecular Biology and 9 papers in Cognitive Neuroscience. Recurrent topics in Melissa T. Carter's work include Genomic variations and chromosomal abnormalities (10 papers), Autism Spectrum Disorder Research (9 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Melissa T. Carter is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Autism Spectrum Disorder Research (9 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Melissa T. Carter collaborates with scholars based in Canada, United States and Saudi Arabia. Melissa T. Carter's co-authors include Kym M. Boycott, Tracy Yuen, Wendy J. Ungar, Péter Szatmári, Beverly S. Emanuel, Elaine H. Zackai, Lijia Huang, Melanie Penner, Jeremy Schwartzentruber and Peter W. Schofield and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Autism and Developmental Disorders and Developmental Medicine & Child Neurology.

In The Last Decade

Melissa T. Carter

33 papers receiving 580 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Melissa T. Carter Canada 16 326 320 103 94 75 34 616
Krzysztof Szczałuba Poland 15 369 1.1× 328 1.0× 67 0.7× 63 0.7× 69 0.9× 57 638
Angela Peron Italy 18 365 1.1× 261 0.8× 127 1.2× 55 0.6× 73 1.0× 54 827
Bhooma Thiruvahindrapuram Canada 14 500 1.5× 420 1.3× 147 1.4× 61 0.6× 123 1.6× 47 880
Amy Yang United States 14 414 1.3× 367 1.1× 194 1.9× 59 0.6× 71 0.9× 28 841
Yaping Yang United States 17 440 1.3× 485 1.5× 48 0.5× 38 0.4× 61 0.8× 35 843
Theresa A. Grebe United States 16 458 1.4× 449 1.4× 102 1.0× 32 0.3× 92 1.2× 34 879
Sofia Douzgou United Kingdom 16 321 1.0× 338 1.1× 75 0.7× 53 0.6× 52 0.7× 49 679
Dominique Martin‐Coignard France 14 424 1.3× 522 1.6× 86 0.8× 36 0.4× 78 1.0× 22 817
Muhammad Mahajnah Israel 16 281 0.9× 391 1.2× 59 0.6× 117 1.2× 59 0.8× 55 831
Rasim Özgür Rosti United States 15 331 1.0× 494 1.5× 62 0.6× 83 0.9× 106 1.4× 32 814

Countries citing papers authored by Melissa T. Carter

Since Specialization
Citations

This map shows the geographic impact of Melissa T. Carter'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 Melissa T. Carter with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Melissa T. Carter more than expected).

Fields of papers citing papers by Melissa T. Carter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Melissa T. Carter. 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 Melissa T. Carter. The network helps show where Melissa T. Carter may publish in the future.

Co-authorship network of co-authors of Melissa T. Carter

This figure shows the co-authorship network connecting the top 25 collaborators of Melissa T. Carter. A scholar is included among the top collaborators of Melissa T. Carter 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 Melissa T. Carter. Melissa T. Carter 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.
2.
Goldman, Sylvie, et al.. (2023). Rett-like Phenotypes in HNRNPH2-Related Neurodevelopmental Disorder. Genes. 14(6). 1154–1154. 1 indexed citations
3.
Zambonin, Jessica L., et al.. (2022). Further clinical delineation of microcephaly‐capillary malformation syndrome. American Journal of Medical Genetics Part A. 188(11). 3350–3357. 3 indexed citations
4.
Walker, Susan, Sylvia Lamoureux, Tayyaba Khan, et al.. (2021). Genome sequencing for detection of pathogenic deep intronic variation: A clinical case report illustrating opportunities and challenges. American Journal of Medical Genetics Part A. 185(10). 3129–3135. 13 indexed citations
5.
Carter, Melissa T., et al.. (2019). Compound heterozygous CACNA1H mutations associated with severe congenital amyotrophy. Channels. 13(1). 153–161. 20 indexed citations
6.
Carter, Melissa T., Sunita Venkateswaran, Jorge Dávila, et al.. (2019). Clinical delineation of GTPBP2 ‐associated neuro‐ectodermal syndrome: Report of two new families and review of the literature. Clinical Genetics. 95(5). 601–606. 12 indexed citations
7.
Bend, Renee, Lior Cohen, Melissa T. Carter, et al.. (2019). Phenotype and mutation expansion of the PTPN23 associated disorder characterized by neurodevelopmental delay and structural brain abnormalities. European Journal of Human Genetics. 28(1). 76–87. 18 indexed citations
8.
Yuen, Tracy, Melanie Penner, Melissa T. Carter, Péter Szatmári, & Wendy J. Ungar. (2018). Assessing the accuracy of the Modified Checklist for Autism in Toddlers: a systematic review and meta‐analysis. Developmental Medicine & Child Neurology. 60(11). 1093–1100. 49 indexed citations
9.
Yuen, Tracy, Melissa T. Carter, Péter Szatmári, & Wendy J. Ungar. (2018). Cost-Effectiveness of Universal or High-Risk Screening Compared to Surveillance Monitoring in Autism Spectrum Disorder. Journal of Autism and Developmental Disorders. 48(9). 2968–2979. 21 indexed citations
10.
Kannus, Pekka, et al.. (2017). <b><i>PLS3</i></b> Mutations in X-Linked Osteoporosis: Clinical and Bone Characteristics of Two Novel Mutations. Hormone Research in Paediatrics. 88(3-4). 298–304. 24 indexed citations
11.
Vasli, Nasim, Kirti Mittal, Anna Mikhailov, et al.. (2015). Identification of a homozygous missense mutation in LRP2 and a hemizygous missense mutation in TSPYL2 in a family with mild intellectual disability. Psychiatric Genetics. 26(2). 66–73. 17 indexed citations
12.
Hashemi, Bita, Anne S. Bassett, David Chitayat, et al.. (2015). Deletion of 15q11.2(BP1‐BP2) region: Further evidence for lack of phenotypic specificity in a pediatric population. American Journal of Medical Genetics Part A. 167(9). 2098–2102. 40 indexed citations
13.
Huang, Lijia, Jodi Warman‐Chardon, Melissa T. Carter, et al.. (2012). Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia. Orphanet Journal of Rare Diseases. 7(1). 67–67. 104 indexed citations
14.
Carter, Melissa T., Michael T. Geraghty, Laura de la Cruz, et al.. (2011). A new syndrome with multiple capillary malformations, intractable seizures, and brain and limb anomalies. American Journal of Medical Genetics Part A. 155(2). 301–306. 23 indexed citations
15.
Carter, Melissa T., Sarah Dyack, & Julie Richer. (2010). Distal trisomy 10q syndrome: phenotypic features in a child with inverted duplicated 10q25.1–q26.3. Clinical Dysmorphology. 19(3). 140–145. 12 indexed citations
16.
Carter, Melissa T., David J. Picketts, Alasdair G. W. Hunter, & Gail E. Graham. (2009). Further clinical delineation of the Börjeson–Forssman–Lehmann syndrome in patients with PHF6 mutations. American Journal of Medical Genetics Part A. 149A(2). 246–250. 23 indexed citations
17.
Carter, Melissa T., et al.. (2009). Risk of breast cancer not increased in translocation 11;22 carriers: Analysis of 80 pedigrees. American Journal of Medical Genetics Part A. 152A(1). 212–214. 16 indexed citations
18.
McMillan, Hugh J., Melissa T. Carter, Pierre Jacob, et al.. (2009). Homozygous contiguous gene deletion of 13q12 causing LGMD2C and ARSACS in the same patient. Muscle & Nerve. 39(3). 396–399. 11 indexed citations
19.
Carter, Melissa T., et al.. (2009). Phenotypic delineation of Emanuel syndrome (supernumerary derivative 22 syndrome): Clinical features of 63 individuals. American Journal of Medical Genetics Part A. 149A(8). 1712–1721. 74 indexed citations
20.
Nowaczyk, Małgorzata J.M., Melissa T. Carter, Jie Xu, et al.. (2008). Paternal deletion 6q24.3: A new congenital anomaly syndrome associated with intrauterine growth failure, early developmental delay and characteristic facial appearance. American Journal of Medical Genetics Part A. 146A(3). 354–360. 20 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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