Rhinda Goedken

2.1k total citations
15 papers, 536 citations indexed

About

Rhinda Goedken is a scholar working on Genetics, Cognitive Neuroscience and Clinical Psychology. According to data from OpenAlex, Rhinda Goedken has authored 15 papers receiving a total of 536 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 7 papers in Cognitive Neuroscience and 3 papers in Clinical Psychology. Recurrent topics in Rhinda Goedken's work include Autism Spectrum Disorder Research (7 papers), Genetic Associations and Epidemiology (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Rhinda Goedken is often cited by papers focused on Autism Spectrum Disorder Research (7 papers), Genetic Associations and Epidemiology (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Rhinda Goedken collaborates with scholars based in United States, France and Canada. Rhinda Goedken's co-authors include Veronica J. Vieland, Val C. Sheffield, Thomas H. Wassink, Susan E. Folstein, Raymond R. Crowe, Joseph Piven, Joseph Piven, Christopher W. Bartlett, Russell Noyes and Jeffrey J. Nelson and has published in prestigious journals such as PLoS ONE, The American Journal of Human Genetics and Molecular Psychiatry.

In The Last Decade

Rhinda Goedken

15 papers receiving 528 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Rhinda Goedken United States	10	272	170	144	134	67	15	536
Ohiko Hashimoto Japan	12	229 0.8×	261 1.5×	158 1.1×	159 1.2×	97 1.4×	28	659
D Gonen United States	8	358 1.3×	375 2.2×	160 1.1×	167 1.2×	111 1.7×	9	658
Isabelle Meresse France	7	134 0.5×	389 2.3×	70 0.5×	79 0.6×	61 0.9×	7	637
Desmond P. Kelly United States	13	201 0.7×	223 1.3×	143 1.0×	31 0.2×	80 1.2×	29	549
William J. Cutter United Kingdom	12	305 1.1×	276 1.6×	212 1.5×	27 0.2×	71 1.1×	16	659
Suping Wu China	6	183 0.7×	166 1.0×	129 0.9×	340 2.5×	112 1.7×	9	599
Rayna Azuma United Kingdom	10	131 0.5×	421 2.5×	295 2.0×	67 0.5×	66 1.0×	12	846
Nicole Barger United States	12	134 0.5×	252 1.5×	140 1.0×	127 0.9×	18 0.3×	14	548
Giuseppe Doneddu Italy	10	121 0.4×	218 1.3×	79 0.5×	81 0.6×	55 0.8×	18	441
David S. Hong United States	19	649 2.4×	385 2.3×	317 2.2×	39 0.3×	42 0.6×	51	1.1k

Countries citing papers authored by Rhinda Goedken

Since Specialization

Citations

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

Fields of papers citing papers by Rhinda Goedken

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rhinda Goedken

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

All Works

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15 of 15 papers shown

Ye, Xiaoqian, Audrey Guilmatre, Boris Reva, et al.. (2016). Mutation Screening of Candidate Genes in Patients with Nonsyndromic Sagittal Craniosynostosis. Plastic & Reconstructive Surgery. 137(3). 952–961. 19 indexed citations

Botto, Lorenzo D., Timothy J. Flood, Julian Little, et al.. (2013). Cancer Risk in Children and Adolescents with Birth Defects: A Population-Based Cohort Study. PLoS ONE. 8(7). e69077–e69077. 62 indexed citations

Wassink, Thomas H., Veronica J. Vieland, Val C. Sheffield, et al.. (2008). Posterior probability of linkage analysis of autism dataset identifies linkage to chromosome 16. Psychiatric Genetics. 18(2). 85–91. 7 indexed citations

Wassink, Thomas H., Molly Losh, Veronica J. Vieland, et al.. (2005). A case of autism and uniparental disomy of chromosome 1. Human Genetics. 117(2-3). 200–206. 12 indexed citations

Bartlett, Christopher W., Rhinda Goedken, & Veronica J. Vieland. (2005). Effects of Updating Linkage Evidence across Subsets of Data: Reanalysis of the Autism Genetic Resource Exchange Data Set. The American Journal of Human Genetics. 76(4). 688–695. 24 indexed citations

Wassink, Thomas H., Joseph Piven, Veronica J. Vieland, et al.. (2005). Evaluation of the chromosome 2q37.3 geneCENTG2as an autism susceptibility gene. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 136B(1). 36–44. 57 indexed citations

Wassink, Thomas H., Joseph Piven, Veronica J. Vieland, et al.. (2004). Examination of AVPR1a as an autism susceptibility gene. Molecular Psychiatry. 9(10). 968–972. 154 indexed citations

Logue, Mark W., Rhinda Goedken, & Veronica J. Vieland. (2003). A model-integrated multipoint Bayesian analysis of hypertension in the Framingham Heart Study data finds little evidence of linkage. BMC Genetics. 4(Suppl 1). S75–S75. 1 indexed citations

Logue, Mark W., Veronica J. Vieland, Rhinda Goedken, & Raymond R. Crowe. (2003). Bayesian analysis of a previously published genome screen for panic disorder reveals new and compelling evidence for linkage to chromosome 7. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 121B(1). 95–99. 50 indexed citations

10.

Wassink, Thomas H., Joseph Piven, Veronica J. Vieland, et al.. (2002). Evaluation of FOXP2 as an autism susceptibility gene. American Journal of Medical Genetics. 114(5). 566–569. 61 indexed citations

11.

Philibert, Robert A., Jeffrey J. Nelson, Bruce Bedell, et al.. (2002). Role of elastin polymorphisms in panic disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 117B(1). 7–10. 5 indexed citations

12.

Crowe, Raymond R., et al.. (2001). Genomewide survey of panic disorder. American Journal of Medical Genetics. 105(1). 105–109. 71 indexed citations

13.

Crowe, Raymond R., et al.. (2001). Genomewide survey of panic disorder. American Journal of Medical Genetics. 105(1). 105–109. 1 indexed citations

14.

Goedken, Rhinda, Elizabeth Ludington, R R Crowe, et al.. (2000). Drawbacks of GENEHUNTER for larger pedigrees: Application to panic disorder. American Journal of Medical Genetics. 96(6). 781–783. 10 indexed citations

15.

Wesner, Robert B., Vasantkumar L. Tanna, Pat Palmer, et al.. (1990). Linkage of c-Harvey-ras-1 and INS DNA markers to unipolar depression and alcoholism is ruled out in 18 families. European Archives of Psychiatry and Clinical Neuroscience. 239(6). 356–360. 2 indexed citations

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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