Lisa G. Shaffer

451 total citations
10 papers, 302 citations indexed

About

Lisa G. Shaffer is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Lisa G. Shaffer has authored 10 papers receiving a total of 302 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Lisa G. Shaffer's work include Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Hereditary Neurological Disorders (3 papers). Lisa G. Shaffer is often cited by papers focused on Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Hereditary Neurological Disorders (3 papers). Lisa G. Shaffer collaborates with scholars based in United States, Mexico and South Korea. Lisa G. Shaffer's co-authors include Lorraine Potocki, Catherine D. Kashork, Christopher McCaskill, Terry Hassold, James R. Lupski, Stuart K. Shapira, Daniel L. Burgess, Jeffrey L. Noebels, Thearith Koeuth and Olivia W. Lee and has published in prestigious journals such as The American Journal of Human Genetics, Epilepsia and American Journal of Medical Genetics.

In The Last Decade

Lisa G. Shaffer

10 papers receiving 291 citations

Peers

Countries citing papers authored by Lisa G. Shaffer

Since Specialization

Citations

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

Fields of papers citing papers by Lisa G. Shaffer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lisa G. Shaffer. 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 Lisa G. Shaffer. The network helps show where Lisa G. Shaffer may publish in the future.

Co-authorship network of co-authors of Lisa G. Shaffer

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

All Works

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10 of 10 papers shown

#	Work	Indexed citations
1	Loss of the Potassium Channel β‐Subunit Gene, KCNAB2, Is Associated with Epilepsy in Patients with 1p36 Deletion Syndrome 2001 ·Epilepsia ·Heidi A. Heilstedt, Daniel L. Burgess, (unknown), Aziza Chedrawi, (unknown), Olivia W. Lee, Catherine D. Kashork, David E. Starkey, Yuanqing Wu, Jeffrey L. Noebels, Lisa G. Shaffer, (unknown)	65
2	Hereditary Neuropathy With Liability to Pressure Palsies Is Not a Major Cause of Idiopathic Carpal Tunnel Syndrome 2001 ·Archives of Neurology ·David W. Stockton, Ricardo A. Meade, David T. Netscher, Michael Epstein, Saleh M. Shenaq, Lisa G. Shaffer, James R. Lupski	12
3	DNA Rearrangements on Both Homologues of Chromosome 17 in a Mildly Delayed Individual with a Family History of Autosomal Dominant Carpal Tunnel Syndrome 1999 ·The American Journal of Human Genetics ·Lorraine Potocki, Ken‐Shiung Chen, Thearith Koeuth, James M. Killian, Susan T. Iannaccone, Stuart K. Shapira, Catherine D. Kashork, Aimee S. Spikes, Lisa G. Shaffer, James R. Lupski	49
4	De novo direct duplication of 15q15?q24 in a newborn boy with mild manifestations 1999 ·American Journal of Medical Genetics ·Jin‐Yeong Han, Kyeong‐Hee Kim, Hye Won Lee, (unknown), Lisa G. Shaffer	5
5	Miller-Dieker syndrome and trisomy 5p in a child carrying a derivative chromosome with a microdeletion in 17p13.3 telomeric to theLIS1 and the D17S379 loci 1999 ·American Journal of Medical Genetics ·Osvaldo M. Mutchinick, Lisa G. Shaffer, Catherine D. Kashork, (unknown)	9
6	Systematic search for uniparental disomy in early fetal losses: The results and a review of the literature 1998 ·American Journal of Medical Genetics ·Lisa G. Shaffer, Christopher McCaskill, (unknown), Terry Hassold	43
7	Inherited duplication Xq27-qter at Xp22.3 in severely affected males: Molecular cytogenetic evaluation and clinical description in three unrelated families 1998 ·American Journal of Medical Genetics ·Barbara K. Goodman, Lisa G. Shaffer, Julie Rutberg, Mary Leppert, (unknown), Sarantis Gagos, (unknown), Martin G. Bialer, (unknown), Beth A. Pletcher, Stuart K. Shapira, Michael T. Geraghty	30
8	Severe clinical phenotype due to an interstitial deletion of the short arm of chromosome 1: A brief review 1997 ·American Journal of Medical Genetics ·David W. Stockton, (unknown), (unknown), (unknown), Lisa G. Shaffer, (unknown)	12
9	Interstitial deletion of 11 (P11.2p12): A newly described contiguous gene deletion syndrome involving the gene for hereditary multiple exostoses (EXT2) 1996 ·American Journal of Medical Genetics ·Lorraine Potocki, Lisa G. Shaffer	56
10	Evidence for a major gene in familial anencephaly 1990 ·American Journal of Medical Genetics ·Lisa G. Shaffer, Mary L. Marazita, Joann Bodurtha, Anna Newlin, W. E. Nance	21

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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