Art Grix

737 total citations
9 papers, 349 citations indexed

About

Art Grix is a scholar working on Genetics, Molecular Biology and Obstetrics and Gynecology. According to data from OpenAlex, Art Grix has authored 9 papers receiving a total of 349 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Obstetrics and Gynecology. Recurrent topics in Art Grix's work include Gestational Diabetes Research and Management (2 papers), Genetic Syndromes and Imprinting (1 paper) and Genomics and Rare Diseases (1 paper). Art Grix is often cited by papers focused on Gestational Diabetes Research and Management (2 papers), Genetic Syndromes and Imprinting (1 paper) and Genomics and Rare Diseases (1 paper). Art Grix collaborates with scholars based in United States, Canada and Switzerland. Art Grix's co-authors include John M. Opitz, Kirk Aleck, Mark Lipson, Bruce R. Korf, Michael L. Cunningham, John B. Mulliken, Ethylin Wang Jabs, William A. Paznekas, Timothy D. Howard and Murray Feingold and has published in prestigious journals such as The American Journal of Human Genetics, American Journal of Medical Genetics and Pediatric Neurology.

In The Last Decade

Art Grix

9 papers receiving 338 citations

Peers

Art Grix

GENET

MB

SURGE

GENET

CB

Magdalena Badura‐Stronka Poland

Bénédicte Demeer France

Gabriela Stangoni Italy

Mónica Rosello Spain

Carole Brewer United Kingdom

Anand Saggar United Kingdom

Dawn Earl United States

Ho‐Ming Luk China

A. J. van Essen Netherlands

Christine A. Oley Australia

Magdalena Badura‐Stronka Poland

Art Grix

141 ×0.6

GENET

183 ×1.0

MB

77 ×1.6

SURGE

23 ×0.8

GENET

20 ×0.7

CB

Citations per year, relative to Art Grix Art Grix (= 1×) peers Magdalena Badura‐Stronka

Countries citing papers authored by Art Grix

Since Specialization

Citations

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

Fields of papers citing papers by Art Grix

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Art Grix

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

9 of 9 papers shown

1.

Mirzaa, Ghayda, Alex R. Paciorkowski, Eric D. Marsh, et al.. (2013). CDKL5 and ARX Mutations in Males With Early-Onset Epilepsy. Pediatric Neurology. 48(5). 367–377. 37 indexed citations

2.

Wong, Lee-Jun, Pu Dai, Duan‐Jun Tan, et al.. (2001). Severe lactic acidosis caused by a novel frame-shift mutation in mitochondrial-encoded cytochrome c oxidase subunit II. American Journal of Medical Genetics. 102(1). 95–99. 27 indexed citations

3.

Paznekas, William A., Michael L. Cunningham, Timothy D. Howard, et al.. (1998). Genetic Heterogeneity of Saethre-Chotzen Syndrome, Due to TWIST and FGFR Mutations. The American Journal of Human Genetics. 62(6). 1370–1380. 160 indexed citations

4.

Chitayat, David, Art Grix, J. Williamson Balfe, et al.. (1997). Brachydactyly-short stature-hypertension (Bilginturan) syndrome: Report on two families. American Journal of Medical Genetics. 73(3). 279–285. 9 indexed citations

5.

Johnston, Kathreen, Mahin Golabi, Bryan D. Hall, et al.. (1987). Alopecia‐anosmia‐deafness‐hypogonadism syndrome revisited: Report of a new case. American Journal of Medical Genetics. 26(4). 925–927. 9 indexed citations

6.

Aleck, Kirk, Art Grix, Carol L. Clericuzio, et al.. (1987). Dyssegmental dysplasias: Clinical, radiographic, and morphologic evidence of heterogeneity. American Journal of Medical Genetics. 27(2). 295–312. 35 indexed citations

7.

Grix, Art & John M. Opitz. (1982). Malformations in infants of diabetic mothers. American Journal of Medical Genetics. 13(2). 131–137. 52 indexed citations

8.

Grix, Art, et al.. (1982). Patterns of multiple malformations in infants of diabetic mothers.. PubMed. 18(3 Pt A). 55–77. 18 indexed citations

9.

Grix, Art, Willard J. Blankenship, Rebecca Peterson, & Bryan D. Hall. (1975). A new familial syndrome with craniofacial abnormalities, osseous defects and mental retardation.. PubMed. 11(5). 107–14. 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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