Amy Knight Johnson

889 total citations
16 papers, 396 citations indexed

About

Amy Knight Johnson is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Amy Knight Johnson has authored 16 papers receiving a total of 396 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 3 papers in Surgery and 3 papers in Molecular Biology. Recurrent topics in Amy Knight Johnson's work include Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and BRCA gene mutations in cancer (3 papers). Amy Knight Johnson is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and BRCA gene mutations in cancer (3 papers). Amy Knight Johnson collaborates with scholars based in United States, Canada and Australia. Amy Knight Johnson's co-authors include Daniela del Gaudio, Soma Das, Barry H. Margolin, Raymond W. Tennant, Kenneth R. Tindall, Walter W. Piegorsch, John E. French, Michael D. Shelby, Lucia Guidugli and Rochelle N. Naylor and has published in prestigious journals such as Journal of Clinical Oncology, Leukemia and Genetics in Medicine.

In The Last Decade

Amy Knight Johnson

16 papers receiving 391 citations

Peers

Countries citing papers authored by Amy Knight Johnson

Since Specialization

Citations

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

Fields of papers citing papers by Amy Knight Johnson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Amy Knight Johnson. 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 Amy Knight Johnson. The network helps show where Amy Knight Johnson may publish in the future.

Co-authorship network of co-authors of Amy Knight Johnson

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

All Works

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16 of 16 papers shown

#	Work	Indexed citations
1	Adapting ACMG/AMP sequence variant classification guidelines for single-gene copy number variants 2019 ·Genetics in Medicine ·Tracy Brandt, Laura M. Sack, Dolores Arjona, (unknown), Hui Mei, Hong Cui, Hua Gao, Lora Jh Bean, Arunkanth Ankala, Daniela del Gaudio, Amy Knight Johnson, Lisa M. Vincent, (unknown), (unknown), Gabriele Richard, Jeanne Meck	88
2	Variant interpretation is a component of clinical practice among genetic counselors in multiple specialties 2019 ·Genetics in Medicine ·Karen E. Wain, Danielle R. Azzariti, Jennifer Goldstein, Amy Knight Johnson, Patti Krautscheid, (unknown), Julianne O’Daniel, Deborah Ritter, Juliann M. Savatt, Erin Rooney Riggs, Christa Lese Martin	16
3	Targeted exome analysis identifies the genetic basis of disease in over 50% of patients with a wide range of ataxia-related phenotypes 2018 ·Genetics in Medicine ·Miao Sun, Amy Knight Johnson, Viswateja Nelakuditi, Lucia Guidugli, David S. Fischer, Kelly Arndt, Lan Ma, Erin Sandford, Vikram G. Shakkottai, Kym M. Boycott, Jodi Warman‐Chardon, Zejuan Li, Daniela del Gaudio, Margit Burmeister, Christopher M. Gómez, Darrel Waggoner, Soma Das	49
4	Maturity-Onset Diabetes of the Young Overview 2018 ·Rochelle N. Naylor, Amy Knight Johnson, Daniela del Gaudio	25
5	Frequency of germline mutations in cancer susceptibility genes in malignant mesothelioma. 2018 ·Journal of Clinical Oncology ·Vasiliki Panou, (unknown), (unknown), Caroline Weipert, (unknown), Aliya N. Husain, Jyoti D. Patel, Buerkley Rose, Viswateja Nelakuditi, Amy Knight Johnson, (unknown), David S. Fischer, Nanna Sulai, Kiran K. Turaga, Dezheng Huo, (unknown), Sabah Kadri, Zejuan Li, Hedy L. Kindler, Jane E. Churpek	14
6	Molecular characterization of HDAC8 deletions in individuals with atypical Cornelia de Lange syndrome 2017 ·Journal of Human Genetics ·(unknown), Jennifer Keller‐Ramey, Amy Knight Johnson, Jennifer A. Lee, Daniel B. Magner, (unknown), (unknown), (unknown), Zejuan Li, (unknown), Soma Das, Rachel Laframboise, (unknown), Ian D. Krantz, Sarah E. Noon, George Hoganson, Jennifer Burton, Christian P. Schaaf, Daniela del Gaudio	10
7	Clinical utility of gene panel-based testing for hereditary myelodysplastic syndrome/acute leukemia predisposition syndromes 2017 ·Leukemia ·Lucia Guidugli, Amy Knight Johnson, Gorka Alkorta‐Aranburu, Viswateja Nelakuditi, Kelly Arndt, Jane E. Churpek, Lucy A. Godley, (unknown), Neal S. Young, Carrie Fitzpatrick, Daniela del Gaudio, Soma Das, (unknown)	32
8	Alu‐mediated deletion of PIGL in a Patient with CHIME syndrome 2017 ·American Journal of Medical Genetics Part A ·Amy Knight Johnson, G. Bradley Schaefer, Jennifer Lee, (unknown), Daniela del Gaudio	14
9	Improved molecular diagnosis of patients with neonatal diabetes using a combined next-generation sequencing and MS-MLPA approach 2016 ·Journal of Pediatric Endocrinology and Metabolism ·Gorka Alkorta‐Aranburu, Madina Sukhanova, David Carmody, Trevor L. Hoffman, (unknown), Jennifer Keller‐Ramey, Zejuan Li, Amy Knight Johnson, (unknown), (unknown), Carrie Fitzpatrick, Soma Das, Daniela del Gaudio	16
10	Evaluation of laboratory perspectives on hereditary cancer panels 2016 ·Familial Cancer ·Jessica Stoll, Scott M. Weissman, (unknown), Christina G. Selkirk, Amy Knight Johnson, Anna Newlin, Kristen J. Vogel Postula	3
11	<em>In Vivo</em> and <em>Ex Vivo</em> Approaches to Study Ovarian Cancer Metastatic Colonization of Milky Spot Structures in Peritoneal Adipose 2015 ·Journal of Visualized Experiments ·Venkatesh Krishnan, R. J. H. Clark, Marina Chekmareva, Amy Knight Johnson, Sophia George, Patricia Shaw, Victoria L. Seewaldt, Carrie Rinker‐Schaeffer	9
12	A novel mutation in the promoter of RARS2 causes pontocerebellar hypoplasia in two siblings 2015 ·Journal of Human Genetics ·Zejuan Li, (unknown), Lucia Guidugli, Amy Knight Johnson, Stephen Arnovitz, Sandra Yang, Joseph Scafidi, Marshall Summar, Gilbert Vézina, Soma Das, Kimberly A. Chapman, Daniela del Gaudio	27
13	Reinitiation of mRNA translation in a patient with X-linked infantile spasms with a protein-truncating variant in ARX 2015 ·European Journal of Human Genetics ·(unknown), Scott Topper, MARY N. KARN, Amy Knight Johnson, Soma Das, Jorge Vidaurre, Cheryl Shoubridge	11
14	<em>In Vivo</em> and <em>Ex Vivo</em> Approaches to Study Ovarian Cancer Metastatic Colonization of Milky Spot Structures in Peritoneal Adipose 2015 ·Journal of Visualized Experiments ·Venkatesh Krishnan, R. J. H. Clark, Marina Chekmareva, Amy Knight Johnson, Sophia George, Patricia Shaw, Victoria L. Seewaldt, Carrie Rinker‐Schaeffer	3
15	Inflammatory pseudotumor of the heart caused by Listeria monocytogenes infection 2009 ·Journal of Infection ·Amos Adler, (unknown), John Marcinak, Amy Knight Johnson, Xiaotian Zheng, Susan L. Hasegawa, Stanford T. Shulman	18
16	Study design and sample sizes for a lacl transgenic mouse mutation assay 1995 ·Environmental and Molecular Mutagenesis ·Walter W. Piegorsch, Barry H. Margolin, Michael D. Shelby, Amy Knight Johnson, John E. French, Raymond W. Tennant, Kenneth R. Tindall	61

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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