Carrie Hanscom

3.0k total citations
10 papers, 487 citations indexed

About

Carrie Hanscom is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Carrie Hanscom has authored 10 papers receiving a total of 487 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 5 papers in Molecular Biology and 3 papers in Plant Science. Recurrent topics in Carrie Hanscom's work include Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (5 papers) and Chromosomal and Genetic Variations (3 papers). Carrie Hanscom is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (5 papers) and Chromosomal and Genetic Variations (3 papers). Carrie Hanscom collaborates with scholars based in United States, United Kingdom and New Zealand. Carrie Hanscom's co-authors include Michael E. Talkowski, Cynthia C. Morton, James F. Gusella, Vamsee Pillalamarri, Jill A. Rosenfeld, Zehra Ordulu, Colby Chiang, Carl Ernst, Ian Blumenthal and Amelia M. Lindgren and has published in prestigious journals such as New England Journal of Medicine, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Carrie Hanscom

10 papers receiving 468 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Carrie Hanscom United States	10	357	207	132	93	53	10	487
Sophie Brisset France	16	378 1.1×	194 0.9×	183 1.4×	133 1.4×	20 0.4×	39	585
Elisabeth A. Keitges United States	11	439 1.2×	249 1.2×	85 0.6×	105 1.1×	15 0.3×	13	529
Tracy Brandt United States	10	399 1.1×	286 1.4×	82 0.6×	35 0.4×	42 0.8×	14	581
Mariana Moysés‐Oliveira Brazil	11	206 0.6×	130 0.6×	53 0.4×	35 0.4×	17 0.3×	45	300
B Delobel France	11	313 0.9×	170 0.8×	117 0.9×	85 0.9×	9 0.2×	18	451
T. Lukusa Belgium	10	287 0.8×	214 1.0×	70 0.5×	89 1.0×	22 0.4×	32	397
Hiba Risheg United States	10	403 1.1×	374 1.8×	164 1.2×	53 0.6×	21 0.4×	13	640
A.J.H. Hamers Netherlands	15	418 1.2×	220 1.1×	199 1.5×	178 1.9×	7 0.1×	33	560
Mónica Rosello Spain	14	360 1.0×	295 1.4×	95 0.7×	47 0.5×	22 0.4×	41	535
Elisabeth Syk Lundberg Sweden	10	120 0.3×	115 0.6×	51 0.4×	52 0.6×	22 0.4×	13	257

Countries citing papers authored by Carrie Hanscom

Since Specialization

Citations

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

Fields of papers citing papers by Carrie Hanscom

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carrie Hanscom

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

All Works

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10 of 10 papers shown

Schilit, Samantha L.P., Corinna Friedrich, Tammy Kammin, et al.. (2019). SYCP2 Translocation-Mediated Dysregulation and Frameshift Variants Cause Human Male Infertility. The American Journal of Human Genetics. 106(1). 41–57. 66 indexed citations

Jacobsen, Jessie C., Serkan Erdin, Colby Chiang, et al.. (2017). Potential molecular consequences of transgene integration: The R6/2 mouse example. Scientific Reports. 7(1). 9 indexed citations

Schilit, Samantha L.P., Benjamin Currall, Ruen Yao, et al.. (2016). Estrogen-related receptor gamma implicated in a phenotype including hearing loss and mild developmental delay. European Journal of Human Genetics. 24(11). 1622–1626. 14 indexed citations

Brand, Harrison, Ryan L. Collins, Carrie Hanscom, et al.. (2015). Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural Variation. The American Journal of Human Genetics. 97(1). 170–176. 37 indexed citations

Brand, Harrison, Vamsee Pillalamarri, Ryan L. Collins, et al.. (2014). Cryptic and Complex Chromosomal Aberrations in Early-Onset Neuropsychiatric Disorders. The American Journal of Human Genetics. 95(4). 454–461. 27 indexed citations

Macera, Michael J., Brynn Levy, Vaidehi Jobanputra, et al.. (2014). Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole‐genome sequencing. Prenatal Diagnosis. 35(3). 299–301. 27 indexed citations

Hanscom, Carrie & Michael E. Talkowski. (2014). Design of Large‐Insert Jumping Libraries for Structural Variant Detection Using Illumina Sequencing. Current Protocols in Human Genetics. 80(1). 7.22.1–7.22.9. 17 indexed citations

Lindgren, Amelia M., Michael E. Talkowski, Carrie Hanscom, et al.. (2013). Haploinsufficiency of KDM6A is associated with severe psychomotor retardation, global growth restriction, seizures and cleft palate. Human Genetics. 132(5). 537–552. 51 indexed citations

Talkowski, Michael E., Zehra Ordulu, Vamsee Pillalamarri, et al.. (2012). Clinical Diagnosis by Whole-Genome Sequencing of a Prenatal Sample. New England Journal of Medicine. 367(23). 2226–2232. 119 indexed citations

10.

Talkowski, Michael E., Carl Ernst, Adrian Heilbut, et al.. (2011). Next-Generation Sequencing Strategies Enable Routine Detection of Balanced Chromosome Rearrangements for Clinical Diagnostics and Genetic Research. The American Journal of Human Genetics. 88(4). 469–481. 120 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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