Joseph Peeden

1.3k total citations
11 papers, 638 citations indexed

About

Joseph Peeden is a scholar working on Genetics, Molecular Biology and Urology. According to data from OpenAlex, Joseph Peeden has authored 11 papers receiving a total of 638 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Urology. Recurrent topics in Joseph Peeden's work include Urological Disorders and Treatments (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Pediatric Urology and Nephrology Studies (3 papers). Joseph Peeden is often cited by papers focused on Urological Disorders and Treatments (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Pediatric Urology and Nephrology Studies (3 papers). Joseph Peeden collaborates with scholars based in United States, Belgium and Israel. Joseph Peeden's co-authors include Paul A. Law, Andrew W. Zimmerman, Anne M. Comi, H. Norman Noe, Marian L. Rivas, Robert Wyatt, Alain Colige, Miikka Vikkula, Pascal Brouillard and Raphaël Helaers and has published in prestigious journals such as PEDIATRICS, Human Molecular Genetics and The Journal of Urology.

In The Last Decade

Joseph Peeden

11 papers receiving 617 citations

Peers

Joseph Peeden

CN

GENET

PPCH

MB

UROLO

David E. McGinnis United States

Jane H. Dean United States

Blanca Gener Spain

Debora Kidron Israel

Ridha Mrad Tunisia

Giovanni Sorge Italy

Carol E. Anderson United States

Monia Gennari Italy

Bernard N. Chodirker Canada

Henry G. Dunn Canada

David E. McGinnis United States

Joseph Peeden

82 ×0.4

CN

31 ×0.2

GENET

96 ×0.6

PPCH

131 ×1.0

MB

102 ×0.8

UROLO

Citations per year, relative to Joseph Peeden Joseph Peeden (= 1×) peers David E. McGinnis

Countries citing papers authored by Joseph Peeden

Since Specialization

Citations

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

Fields of papers citing papers by Joseph Peeden

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joseph Peeden

This figure shows the co-authorship network connecting the top 25 collaborators of Joseph Peeden. A scholar is included among the top collaborators of Joseph Peeden 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 Joseph Peeden. Joseph Peeden 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:

11 of 11 papers shown

1.

Brouillard, Pascal, Laura Dupont, Raphaël Helaers, et al.. (2017). Loss of ADAMTS3 activity causes Hennekam lymphangiectasia–lymphedema syndrome 3. Human Molecular Genetics. 26(21). 4095–4104. 77 indexed citations

2.

Gozes, Illana, Marc C. Patterson, Anke Van Dijck, et al.. (2017). The Eight and a Half Year Journey of Undiagnosed AD: Gene Sequencing and Funding of Advanced Genetic Testing Has Led to Hope and New Beginnings. Frontiers in Endocrinology. 8. 107–107. 31 indexed citations

3.

El‐Gharbawy, Areeg, Joseph Peeden, Ralph S. Lachman, et al.. (2009). Severe cleidocranial dysplasia and hypophosphatasia in a child with microdeletion of the C‐terminal region of RUNX2. American Journal of Medical Genetics Part A. 152A(1). 169–174. 23 indexed citations

4.

Comi, Anne M., et al.. (1999). Familial Clustering of Autoimmune Disorders and Evaluation of Medical Risk Factors in Autism. Journal of Child Neurology. 14(6). 388–394. 310 indexed citations

5.

Peeden, Joseph, et al.. (1992). Spondylometaphyseal dysplasia, sedaghatian type. American Journal of Medical Genetics. 44(5). 651–656. 12 indexed citations

6.

Noe, H. Norman, Robert Wyatt, Joseph Peeden, & Marian L. Rivas. (1992). The Transmission of Vesicoureteral Reflux from Parent to Child. The Journal of Urology. 148(6). 1869–1871. 108 indexed citations

7.

Peeden, Joseph & H. Norman Noe. (1992). Is It Practical to Screen for Familial Vesicoureteral Reflux Within a Private Pediatric Practice?. PEDIATRICS. 89(4). 758–760. 23 indexed citations

8.

Qumsiyeh, Mazin Β., R. Sid Wilroy, Joseph Peeden, & Avirachan T. Tharapel. (1991). High resolution replication banding combined with in situ hybridization for the delineation of a subtle chromosome rearrangement. American Journal of Medical Genetics. 41(1). 99–101. 5 indexed citations

9.

Noe, H. Norman, Joseph Peeden, Gerald R. Jerkins, & R. Sid Wilroy. (1984). Hypertelorism-Hypospadias Syndrome. The Journal of Urology. 132(5). 951–952. 13 indexed citations

10.

Peeden, Joseph, Kutay Taysi, R. Sid Wilroy, et al.. (1983). Ring chromosome 6: Variability in phenotypic expression. American Journal of Medical Genetics. 16(4). 563–573. 31 indexed citations

11.

Peeden, Joseph, et al.. (1979). Prune perineum. Teratology. 20(2). 233–236. 5 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.

Explore authors with similar magnitude of impact