Katelyn Payne

1.2k total citations
6 papers, 89 citations indexed

About

Katelyn Payne is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Katelyn Payne has authored 6 papers receiving a total of 89 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Neurology. Recurrent topics in Katelyn Payne's work include Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (2 papers) and Neurological disorders and treatments (1 paper). Katelyn Payne is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (2 papers) and Neurological disorders and treatments (1 paper). Katelyn Payne collaborates with scholars based in United States, Israel and Czechia. Katelyn Payne's co-authors include Stephen R. Dlouhy, Joanne Wojcieszek, Jill A. Rosenfeld, Berivan Baskin, Hilary J. Vernon, V. Reid Sutton, Pankaj B. Agrawal, Emily Chen, Chester Brown and James R. Lupski and has published in prestigious journals such as The American Journal of Human Genetics, Medical Clinics of North America and Journal of Child Neurology.

In The Last Decade

Katelyn Payne

6 papers receiving 87 citations

Peers

Countries citing papers authored by Katelyn Payne

Since Specialization

Citations

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

Fields of papers citing papers by Katelyn Payne

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katelyn Payne

This figure shows the co-authorship network connecting the top 25 collaborators of Katelyn Payne. A scholar is included among the top collaborators of Katelyn Payne 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 Katelyn Payne. Katelyn Payne 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	ALS Identified: two‐year findings from a sponsored ALS genetic testing program 2024 ·Annals of Clinical and Translational Neurology ·Stephen A. Goutman, Namita Goyal, Katelyn Payne, Coro Paisán‐Ruiz, Varant Kupelian, (unknown), Adele A. Mitchell, (unknown)	2
2	Phenotypic expansion of POGZ‐related intellectual disability syndrome (White‐Sutton syndrome) 2019 ·American Journal of Medical Genetics Part A ·Nurit Assia Batzir, Jennifer E. Posey, Xiaofei Song, Zeynep Coban‐Akdemir, Jill A. Rosenfeld, Chester Brown, Emily Chen, (unknown), (unknown), (unknown), Katelyn Payne, Annick Raas‐Rothschild, Richard H. Scott, Hilary J. Vernon, Neda Zadeh, James R. Lupski, V. Reid Sutton	30
3	Approach to Assessment of Parkinson Disease with Emphasis on Genetic Testing 2019 ·Medical Clinics of North America ·Katelyn Payne, (unknown), Joanne Wojcieszek	9
4	The progression of Wiedemann–Steiner syndrome in adulthood and two novel variants in the KMT2A gene 2018 ·American Journal of Medical Genetics Part A ·(unknown), Stephen R. Dlouhy, (unknown), Katelyn Payne, David D. Weaver	10
5	Novel Homozygous Deletion in STRADA Gene Associated With Polyhydramnios, Megalencephaly, and Epilepsy in 2 Siblings: Implications for Diagnosis and Treatment 2018 ·Journal of Child Neurology ·K. D. Nelson, (unknown), (unknown), Chie‐Schin Shih, Katelyn Payne, Stephen R. Dlouhy, Laurence E. Walsh	4
6	Heterozygous De Novo UBTF Gain-of-Function Variant Is Associated with Neurodegeneration in Childhood 2017 ·The American Journal of Human Genetics ·Simon Edvardson, Claudia M. Nicolae, Pankaj B. Agrawal, Cyril Mignot, Katelyn Payne, Asuri N. Prasad, Chitra Prasad, Laurie S. Sadler, Caroline Nava, Thomas E. Mullen, Amber Begtrup, Berivan Baskin, Zöe Powis, Avraham Shaag, Boris Keren, George‐Lucian Moldovan, Orly Elpeleg	34

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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