Kim Jenny

525 total citations
6 papers, 265 citations indexed

About

Kim Jenny is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Kim Jenny has authored 6 papers receiving a total of 265 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Kim Jenny's work include Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Genomics and Rare Diseases (1 paper). Kim Jenny is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Genomics and Rare Diseases (1 paper). Kim Jenny collaborates with scholars based in United States, United Kingdom and Germany. Kim Jenny's co-authors include Karen W. Gripp, Elaine H. Zackai, Jonathan Salvin, Deepika Thacker, Elizabeth Hopkins, V. Reid Sutton, Hao Hu, James R. Lupski, Brett H. Graham and Thomas F. Wienker and has published in prestigious journals such as Neurology, Genetics in Medicine and Genome Medicine.

In The Last Decade

Kim Jenny

5 papers receiving 253 citations

Peers

Countries citing papers authored by Kim Jenny

Since Specialization

Citations

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

Fields of papers citing papers by Kim Jenny

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kim Jenny

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

All Works

Sort: Min cites: Since: Top N: Style:

6 of 6 papers shown

#	Work	Indexed citations
1	The Importance of Offering Genetic Counseling and Testing to All Persons Diagnosed With Frontotemporal Degeneration Spectrum Disorders 2025 ·Neurology ·(unknown), Kim Jenny, Kristiana Salmon, Ashley Crook, Wendy R. Uhlmann, Jamie Fong, Jill Goldman, (unknown), Rhona MacLeod, (unknown), Diane Lucente, (unknown), (unknown), Weiyi Mu	0
2	Maternal uniparental disomy of chromosome 20: a novel imprinting disorder of growth failure 2015 ·Genetics in Medicine ·Surabhi Mulchandani, Elizabeth Bhoj, Minjie Luo, Nina Powell‐Hamilton, Kim Jenny, Karen W. Gripp, Miriam Elbracht, Thomas Eggermann, Claire Turner, I. Karen Temple, Deborah Mackay, Holly Dubbs, David A. Stevenson, Leah Slattery, Elaine H. Zackai, Nancy B. Spinner, Ian D. Krantz, Laura K. Conlin	73
3	De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome 2013 ·Genome Medicine ·Matthew N. Bainbridge, Hao Hu, Donna M. Muzny, Luciana Musante, James R. Lupski, Brett H. Graham, Wei Chen, Karen W. Gripp, Kim Jenny, Thomas F. Wienker, Yaping Yang, V. Reid Sutton, Richard A. Gibbs, Hans‐Hilger Ropers	102
4	Expanding the SHOC2 mutation associated phenotype of noonan syndrome with loose anagen hair: Structural brain anomalies and myelofibrosis 2013 ·American Journal of Medical Genetics Part A ·Karen W. Gripp, Dina J. Zand, Laurie Demmer, Carol E. Anderson, William B. Dobyns, Elaine H. Zackai, Elizabeth H. Denenberg, Kim Jenny, Deborah L. Stabley, Katia Sol‐Church	49
5	Cardiac anomalies in Axenfeld–Rieger syndrome due to a novel FOXC1 mutation 2012 ·American Journal of Medical Genetics Part A ·Karen W. Gripp, Elizabeth Hopkins, Kim Jenny, Deepika Thacker, Jonathan Salvin	39
6	Agenesis of the corpus callosum and congenital lymphedema: A novel recognizable syndrome? 2010 ·American Journal of Medical Genetics Part A ·Mary O’Driscoll, Kim Jenny, Sulagna C. Saitta, William B. Dobyns, Karen W. Gripp	2

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.

Explore authors with similar magnitude of impact