Jadd M. Stevens

420 total citations
6 papers, 84 citations indexed

About

Jadd M. Stevens is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Jadd M. Stevens has authored 6 papers receiving a total of 84 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Jadd M. Stevens's work include Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Jadd M. Stevens is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Jadd M. Stevens collaborates with scholars based in United States, Denmark and Canada. Jadd M. Stevens's co-authors include Warren G. Sanger, Ann Haskins Olney, Diane L. Pickering, Bhavana J. Davé, James D. Eudy, Eric T. Rush, Jennifer N. Sanmann, Stephen G. Kahler, Małgorzata J.M. Nowaczyk and Maria Kirchhoff and has published in prestigious journals such as Genetics in Medicine, Leukemia Research and American Journal of Medical Genetics Part A.

In The Last Decade

Jadd M. Stevens

6 papers receiving 82 citations

Peers

Countries citing papers authored by Jadd M. Stevens

Since Specialization

Citations

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

Fields of papers citing papers by Jadd M. Stevens

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jadd M. Stevens. 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 Jadd M. Stevens. The network helps show where Jadd M. Stevens may publish in the future.

Co-authorship network of co-authors of Jadd M. Stevens

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

All Works

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6 of 6 papers shown

#	Work	Indexed citations
1	Frequency, variations, and prognostic implications of chromosome 14q32 deletions in chronic lymphocytic leukemia 2021 ·Leukemia Research ·(unknown), Jadd M. Stevens, Diane L. Pickering, Pamela A. Althof, Lynette M. Smith, Jennifer N. Sanmann, Bhavana J. Davé	3
2	Assessing the utility of confirmatory studies following identification of large-scale genomic imbalances by microarray 2015 ·Genetics in Medicine ·Jennifer N. Sanmann, Diane L. Pickering, (unknown), Jadd M. Stevens, Thomas Hempel, Pamela A. Althof, (unknown), Lois J. Starr, Bhavana J. Davé, Warren G. Sanger	5
3	Report of a patient with developmental delay, hearing loss, growth retardation, and cleft lip and palate and a deletion of 7q34‐36.1: Review of distal 7q deletions 2013 ·American Journal of Medical Genetics Part A ·Eric T. Rush, Jadd M. Stevens, Warren G. Sanger, Ann Haskins Olney	11
4	Characterization of six novel patients with MECP2 duplications due to unbalanced rearrangements of the X chromosome 2012 ·American Journal of Medical Genetics Part A ·Jennifer N. Sanmann, (unknown), Lois J. Starr, (unknown), Diane L. Pickering, Jadd M. Stevens, Stephen G. Kahler, Ann Haskins Olney, G. Bradley Schaefer, Warren G. Sanger	19
5	Microdeletion in distal 17p13.1: A recognizable phenotype with microcephaly, distinctive facial features, and intellectual disability 2012 ·American Journal of Medical Genetics Part A ·Susan Zeesman, Susanne Kjærgaard, Hanne Hove, Maria Kirchhoff, Jadd M. Stevens, Małgorzata J.M. Nowaczyk	9
6	Array-based comparative genomic hybridization analysis of 1176 consecutive clinical genetics investigations 2008 ·Genetics in Medicine ·Diane L. Pickering, James D. Eudy, Ann Haskins Olney, Bhavana J. Davé, (unknown), Jadd M. Stevens, Warren G. Sanger	37

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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