Melissa T. Carter

5.3k citations

34 papers · 616 indexed · h-index 16

Co-authors: Kym M. Boycott Tracy Yuen Péter Szatmári Wendy J. Ungar Beverly S. Emanuel Elaine H. Zackai Lijia Huang Melanie Penner
Topics: Genomic variations and chromosomal abnormalities (10 papers)Autism Spectrum Disorder Research (9 papers)Genetics and Neurodevelopmental Disorders (8 papers)
Cited by: Genetics Cognitive Neuroscience Cellular and Molecular Neuroscience
Journals: SHILAP Revista de lepidopterologíaJournal of Autism and Developmental Disorders Developmental Medicine & Child Neurology
Partner nations: Canada United States Saudi Arabia

In The Last Decade

Melissa T. Carter

33 papers receiving 580 citations

Peers

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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	The diagnostic yield of genetic and metabolic investigations in syndromic and nonsyndromic patients with autism spectrum disorder, global developmental delay, or intellectual disability from a dedicated neurodevelopmental disorders genetics clinic 2024 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),Stan Kutcher,Richard Webster,M. Cloutier,Danielle K. Bourque,(unknown),Melissa T. Carter	2
2	Rett-like Phenotypes in HNRNPH2-Related Neurodevelopmental Disorder 2023 ·Genes ·(unknown),Sylvie Goldman,Melissa T. Carter,Jennifer Bain	1
3	Further clinical delineation of microcephaly‐capillary malformation syndrome 2022 ·American Journal of Medical Genetics Part A ·(unknown),Jessica L. Zambonin,(unknown),Suad Alyamani,John M. Graham,Fowzan S. Alkuraya,(unknown),Melissa T. Carter	3
4	Genome sequencing for detection of pathogenic deep intronic variation: A clinical case report illustrating opportunities and challenges 2021 ·American Journal of Medical Genetics Part A ·Susan Walker,Sylvia Lamoureux,Tayyaba Khan,(unknown),(unknown),Helen M. Branson,Melissa T. Carter,Robin Z. Hayeems,(unknown),Christian R. Marshall,M. Stephen Meyn,Steven P. Miller,Diane Wilson,Stephen W. Scherer,Susan Blasér,Kamiar Mireskandari,Gregory Costain	13
5	Phenotype and mutation expansion of the PTPN23 associated disorder characterized by neurodevelopmental delay and structural brain abnormalities 2019 ·European Journal of Human Genetics ·Renee Bend,Lior Cohen,Melissa T. Carter,Michael J. Lyons,Dmitriy Niyazov,Mohamad A. Mikati,(unknown),Richard Person,Yue Si,Ingrid M. Wentzensen,Erin Torti,Jennifer A. Lee,Kym M. Boycott,Lina Basel‐Vanagaite,Carlos R. Ferreira,Claudia Gonzaga‐Jauregui	18
6	Clinical delineation of GTPBP2 ‐associated neuro‐ectodermal syndrome: Report of two new families and review of the literature 2019 ·Clinical Genetics ·Melissa T. Carter,Sunita Venkateswaran,(unknown),Jorge Dávila,Peter Humphreys,Kristin D. Kernohan,Kym M. Boycott	12
7	Compound heterozygous CACNA1H mutations associated with severe congenital amyotrophy 2019 ·Channels ·Melissa T. Carter,Hugh J. McMillan,(unknown),Norbert Weiss	20
8	Assessing the accuracy of the Modified Checklist for Autism in Toddlers: a systematic review and meta‐analysis 2018 ·Developmental Medicine & Child Neurology ·Tracy Yuen,Melanie Penner,Melissa T. Carter,Péter Szatmári,Wendy J. Ungar	49
9	Cost-Effectiveness of Universal or High-Risk Screening Compared to Surveillance Monitoring in Autism Spectrum Disorder 2018 ·Journal of Autism and Developmental Disorders ·Tracy Yuen,Melissa T. Carter,Péter Szatmári,Wendy J. Ungar	21
10	Cost-effectiveness of Genome and Exome Sequencing in Children Diagnosed with Autism Spectrum Disorder 2018 ·Applied Health Economics and Health Policy ·Tracy Yuen,Melissa T. Carter,Péter Szatmári,Wendy J. Ungar	19
11	<b><i>PLS3</i></b> Mutations in X-Linked Osteoporosis: Clinical and Bone Characteristics of Two Novel Mutations 2017 ·Hormone Research in Paediatrics ·Pekka Kannus,(unknown),Riyana Babul‐Hirji,Melissa T. Carter,Jennifer Harrington	24
12	Identification of a homozygous missense mutation in LRP2 and a hemizygous missense mutation in TSPYL2 in a family with mild intellectual disability 2015 ·Psychiatric Genetics ·Nasim Vasli,(unknown),Kirti Mittal,(unknown),Anna Mikhailov,Muhammad Rafiq,Attya Bhatti,Melissa T. Carter,Danielle M. Andrade,Muhammad Ayub,John B. Vincent,Peter John	17
13	Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia 2012 ·Orphanet Journal of Rare Diseases ·Lijia Huang,Jodi Warman‐Chardon,Melissa T. Carter,K. Friend,Tracy Dudding,Jeremy Schwartzentruber,Ruobing Zou,Peter W. Schofield,(unknown),Dennis E. Bulman,Kym M. Boycott	104
14	A new syndrome with multiple capillary malformations, intractable seizures, and brain and limb anomalies 2011 ·American Journal of Medical Genetics Part A ·Melissa T. Carter,Michael T. Geraghty,Laura de la Cruz,R. Ross Reichard,Luigi Boccuto,Charles E. Schwartz,Carol L. Clericuzio	23
15	Distal trisomy 10q syndrome: phenotypic features in a child with inverted duplicated 10q25.1–q26.3 2010 ·Clinical Dysmorphology ·Melissa T. Carter,Sarah Dyack,Julie Richer	12
16	Further clinical delineation of the Börjeson–Forssman–Lehmann syndrome in patients with PHF6 mutations 2009 ·American Journal of Medical Genetics Part A ·Melissa T. Carter,David J. Picketts,Alasdair G. W. Hunter,Gail E. Graham	23
17	Homozygous contiguous gene deletion of 13q12 causing LGMD2C and ARSACS in the same patient 2009 ·Muscle & Nerve ·Hugh J. McMillan,Melissa T. Carter,Pierre Jacob,Eoghan Laffan,Michael D. O’Connor,Kym M. Boycott	11
18	Phenotypic delineation of Emanuel syndrome (supernumerary derivative 22 syndrome): Clinical features of 63 individuals 2009 ·American Journal of Medical Genetics Part A ·Melissa T. Carter,(unknown),Elaine H. Zackai,Beverly S. Emanuel,Kym M. Boycott	74
19	Risk of breast cancer not increased in translocation 11;22 carriers: Analysis of 80 pedigrees 2009 ·American Journal of Medical Genetics Part A ·Melissa T. Carter,Nicholas Barrowman,(unknown),Beverly S. Emanuel,Kym M. Boycott	16
20	Paternal deletion 6q24.3: A new congenital anomaly syndrome associated with intrauterine growth failure, early developmental delay and characteristic facial appearance 2008 ·American Journal of Medical Genetics Part A ·Małgorzata J.M. Nowaczyk,Melissa T. Carter,Jie Xu,Marlene J. Huggins,Gordana Raca,Soma Das,Christa Lese Martin,Stuart Schwartz,Robert L. Rosenfield,Darrel Waggoner	20

About Melissa T. Carter

Melissa T. Carter is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology, having authored 34 papers that have together received 616 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Autism Spectrum Disorder Research (9 papers) and Genetics and Neurodevelopmental Disorders (8 papers). The work is most often cited by research in Genetics (326 citations), Cognitive Neuroscience (103 citations) and Cellular and Molecular Neuroscience (94 citations). Melissa T. Carter has collaborated with scholars based in Canada, United States and Saudi Arabia. Frequent co-authors include Kym M. Boycott, Tracy Yuen, Péter Szatmári, Wendy J. Ungar, Beverly S. Emanuel, Elaine H. Zackai, Lijia Huang, Melanie Penner, Jodi Warman‐Chardon and Jeremy Schwartzentruber. Their work appears in journals such as SHILAP Revista de lepidopterología, Journal of Autism and Developmental Disorders and Developmental Medicine & Child Neurology.

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.

Explore authors with similar magnitude of impact