Melissa Kramer

6.0k total citations
27 papers, 1.6k citations indexed

About

Melissa Kramer is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Melissa Kramer has authored 27 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 11 papers in Genetics and 6 papers in Cancer Research. Recurrent topics in Melissa Kramer's work include Genomics and Phylogenetic Studies (8 papers), Cancer Genomics and Diagnostics (6 papers) and Genomics and Rare Diseases (5 papers). Melissa Kramer is often cited by papers focused on Genomics and Phylogenetic Studies (8 papers), Cancer Genomics and Diagnostics (6 papers) and Genomics and Rare Diseases (5 papers). Melissa Kramer collaborates with scholars based in United States, United Kingdom and Canada. Melissa Kramer's co-authors include W. Richard McCombie, Emily Hodges, Matthew J. Rodesch, Michael Molla, Thomas J. Albert, Zhenyu Xuan, Vivekanand S. Balija, Gregory J. Hannon, Steven W. Smith and Christina M. Middle and has published in prestigious journals such as Nature Genetics, Journal of Clinical Oncology and Journal of Neuroscience.

In The Last Decade

Melissa Kramer

25 papers receiving 1.6k 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 Kramer United States 15 980 835 448 260 108 27 1.6k
Corinna Menzel Germany 20 1.3k 1.4× 942 1.1× 233 0.5× 456 1.8× 140 1.3× 28 2.1k
Alexandra P MacKenzie United States 6 1.0k 1.0× 838 1.0× 140 0.3× 227 0.9× 341 3.2× 6 1.7k
Sigurjón A. Guðjónsson Iceland 11 1.3k 1.3× 1.5k 1.7× 433 1.0× 108 0.4× 40 0.4× 15 2.4k
Mehdi Zarrei Canada 17 633 0.6× 702 0.8× 340 0.8× 150 0.6× 139 1.3× 59 1.4k
Alexandre S. Cristino Australia 22 714 0.7× 981 1.2× 118 0.3× 256 1.0× 132 1.2× 43 1.9k
Kendra Hoekzema United States 16 686 0.7× 660 0.8× 215 0.5× 97 0.4× 201 1.9× 26 1.3k
Robert S. Illingworth United Kingdom 22 3.8k 3.9× 1.2k 1.4× 380 0.8× 251 1.0× 203 1.9× 29 4.2k
Elena Raimondi Italy 23 845 0.9× 440 0.5× 552 1.2× 118 0.5× 83 0.8× 84 1.5k
Fabian Grubert United States 18 2.3k 2.3× 821 1.0× 519 1.2× 448 1.7× 58 0.5× 20 2.8k
Janet Ziegle United States 17 588 0.6× 894 1.1× 380 0.8× 58 0.2× 45 0.4× 28 1.6k

Countries citing papers authored by Melissa Kramer

Since Specialization
Citations

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

Fields of papers citing papers by Melissa Kramer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Melissa Kramer

This figure shows the co-authorship network connecting the top 25 collaborators of Melissa Kramer. A scholar is included among the top collaborators of Melissa Kramer 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 Kramer. Melissa Kramer 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.
Scheben, Armin, O. Ramos, Melissa Kramer, et al.. (2023). Long-Read Sequencing Reveals Rapid Evolution of Immunity- and Cancer-Related Genes in Bats. Genome Biology and Evolution. 15(9). 28 indexed citations
2.
MacKay‐Brandt, Anna, Melissa Kramer, Kristin Dietz Trautman, et al.. (2022). A longitudinal resource for studying connectome development and its psychiatric associations during childhood. Scientific Data. 9(1). 300–300. 17 indexed citations
3.
Yang, Zhaolin, Xiaoli Wu, Yiliang Wei, et al.. (2021). Transcriptional Silencing of ALDH2 Confers a Dependency on Fanconi Anemia Proteins in Acute Myeloid Leukemia. Cancer Discovery. 11(9). 2300–2315. 20 indexed citations
4.
Malik, Sarah, Chencan Zhu, Jinyu Li, et al.. (2021). Impact of preoperative antibiotics and other variables on integrated microbiome-host transcriptomic data generated from colorectal cancer resections. World Journal of Gastroenterology. 27(14). 1465–1482. 7 indexed citations
5.
Aganezov, Sergey, Sara Goodwin, Rachel M. Sherman, et al.. (2020). Comprehensive analysis of structural variants in breast cancer genomes using single-molecule sequencing. Genome Research. 30(9). 1258–1273. 61 indexed citations
6.
Stec, Natalia, O. Ramos, Nuri Kim, et al.. (2020). ACaenorhabditis elegansModel for Integrating the Functions of Neuropsychiatric Risk Genes Identifies Components Required for Normal Dendritic Morphology. G3 Genes Genomes Genetics. 10(5). 1617–1628. 12 indexed citations
7.
Goodwin, Sara, et al.. (2020). Abstract 1360: Understanding genetic variation in cancer using targeted nanopore long read sequencing. Cancer Research. 80(16_Supplement). 1360–1360. 1 indexed citations
8.
Nattestad, Maria, Sara Goodwin, Karen Ng, et al.. (2018). Complex rearrangements and oncogene amplifications revealed by long-read DNA and RNA sequencing of a breast cancer cell line. Genome Research. 28(8). 1126–1135. 108 indexed citations
9.
Kramer, Melissa, et al.. (2018). A Palpable Back Mass as First Presenting Sign of Acute Lymphoblastic Leukemia in a Pediatric Patient. Journal of Pediatric Hematology/Oncology. 41(1). 77–78.
10.
Ryan, Niamh, Jayon Lihm, Melissa Kramer, et al.. (2018). DNA sequence-level analyses reveal potential phenotypic modifiers in a large family with psychiatric disorders. Molecular Psychiatry. 23(12). 2254–2265. 15 indexed citations
11.
Monson, Eric T., Mehdi Pirooznia, Jennifer Parla, et al.. (2017). Assessment of Whole-Exome Sequence Data in Attempted Suicide within a Bipolar Disorder Cohort. PubMed. 3(1). 1–11. 9 indexed citations
12.
Teng, Shaolei, Pippa A. Thomson, Siobhan McCarthy, et al.. (2017). Rare disruptive variants in the DISC1 Interactome and Regulome: association with cognitive ability and schizophrenia. Molecular Psychiatry. 23(5). 1270–1277. 37 indexed citations
13.
Schatz, Michael C., Lyza Maron, Joshua C. Stein, et al.. (2014). Whole genome de novo assemblies of three divergent strains of rice, Oryza sativa, document novel gene space of aus and indica. Genome biology. 15(11). 506–506. 188 indexed citations
14.
Schatz, Michael C., Lyza Maron, Joshua C. Stein, et al.. (2014). Whole genome de novo assemblies of three divergent strains of rice, Oryza sativa , document novel gene space of aus and indica. Genome Biology. 15(11). 506–506. 152 indexed citations
15.
Pirooznia, Mehdi, Melissa Kramer, Jennifer Parla, et al.. (2014). Validation and assessment of variant calling pipelines for next-generation sequencing. Human Genomics. 8(1). 91 indexed citations
16.
McCarthy, Siobhan, Jesse Gillis, Melissa Kramer, et al.. (2014). De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability. Molecular Psychiatry. 19(6). 652–658. 242 indexed citations
17.
Chen, Yun-Ching, Hannah Carter, Jennifer Parla, et al.. (2013). A Hybrid Likelihood Model for Sequence-Based Disease Association Studies. PLoS Genetics. 9(1). e1003224–e1003224. 14 indexed citations
18.
Tyekucheva, Svitlana, Robert H. Yolken, W. Richard McCombie, et al.. (2011). Establishing the baseline level of repetitive element expression in the human cortex. BMC Genomics. 12(1). 495–495. 11 indexed citations
19.
Parla, Jennifer, et al.. (2011). A comparative analysis of exome capture. Genome biology. 12(9). R97–R97. 85 indexed citations
20.
Hodges, Emily, Zhenyu Xuan, Vivekanand S. Balija, et al.. (2007). Genome-wide in situ exon capture for selective resequencing. Nature Genetics. 39(12). 1522–1527. 485 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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