Arthur W. Grix

687 total citations
6 papers, 197 citations indexed

About

Arthur W. Grix is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Arthur W. Grix has authored 6 papers receiving a total of 197 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 Genetics. Recurrent topics in Arthur W. Grix's work include Genetics and Neurodevelopmental Disorders (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Congenital Ear and Nasal Anomalies (2 papers). Arthur W. Grix is often cited by papers focused on Genetics and Neurodevelopmental Disorders (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Congenital Ear and Nasal Anomalies (2 papers). Arthur W. Grix collaborates with scholars based in United States, France and Australia. Arthur W. Grix's co-authors include John M. Graham, Christa Lese Martin, Richard J. Leventer, Karine Nguyen, Carlos Cardoso, Laurent Villard, Robin M. Winter, William B. Dobyns, Suzanne L. Kilmer and R. Rivkah Isseroff and has published in prestigious journals such as The American Journal of Human Genetics, Journal of the American Academy of Dermatology and American Journal of Medical Genetics.

In The Last Decade

Arthur W. Grix

5 papers receiving 193 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Arthur W. Grix United States	5	105	95	46	28	23	6	197
Emma McCann United Kingdom	6	153 1.5×	177 1.9×	80 1.7×	26 0.9×	10 0.4×	10	315
J A Hurst United Kingdom	4	149 1.4×	319 3.4×	27 0.6×	39 1.4×	28 1.2×	6	372
Martha Schatz United States	6	56 0.5×	91 1.0×	29 0.6×	12 0.4×	18 0.8×	8	236
Nathalie Marle France	11	170 1.6×	237 2.5×	56 1.2×	8 0.3×	42 1.8×	23	373
Shozo Ohdo Japan	9	107 1.0×	117 1.2×	52 1.1×	10 0.4×	7 0.3×	30	224
Eda Ütine Türkiye	9	96 0.9×	99 1.0×	20 0.4×	9 0.3×	16 0.7×	24	218
Shams Anazi Saudi Arabia	9	197 1.9×	181 1.9×	23 0.5×	21 0.8×	20 0.9×	10	273
Mara Cavallin France	9	98 0.9×	74 0.8×	50 1.1×	17 0.6×	40 1.7×	13	185
Chloe Stutterd Australia	9	109 1.0×	135 1.4×	64 1.4×	31 1.1×	24 1.0×	18	283
Abdelhafid Natiq Morocco	6	123 1.2×	80 0.8×	50 1.1×	12 0.4×	19 0.8×	21	216

Countries citing papers authored by Arthur W. Grix

Since Specialization

Citations

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

Fields of papers citing papers by Arthur W. Grix

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arthur W. Grix

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

All Works

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6 of 6 papers shown

1.

Saadi, Irfan, Fowzan S. Alkuraya, Stephen S. Gisselbrecht, et al.. (2011). Deficiency of the Cytoskeletal Protein SPECC1L Leads to Oblique Facial Clefting. The American Journal of Human Genetics. 89(1). 44–55. 55 indexed citations

2.

Carey, John C., Cynthia J. Curry, Arthur W. Grix, et al.. (2003). A tribute to Bryan D. Hall: Festschrift 2003. American Journal of Medical Genetics Part A. 123A(1). 1–4.

3.

Villard, Laurent, Karine Nguyen, Carlos Cardoso, et al.. (2002). A Locus for Bilateral Perisylvian Polymicrogyria Maps to Xq28. The American Journal of Human Genetics. 70(4). 1003–1008. 79 indexed citations

4.

Schnur, Rhonda E., L. Charles Bailey, Timothy R. Rebbeck, et al.. (1994). Phenotypic variability in X-linked ocular albinism: relationship to linkage genotypes.. PubMed. 55(3). 484–96. 19 indexed citations

5.

Kilmer, Suzanne L., Arthur W. Grix, & R. Rivkah Isseroff. (1993). Focal dermal hypoplasia: Four cases with widely varying presentations. Journal of the American Academy of Dermatology. 28(5). 839–843. 17 indexed citations

6.

Hartsfield, James K., et al.. (1993). Pleiotropy in Coffin‐Lowry syndrome: Sensorineural hearing deficit and premature tooth loss as early manifestations. American Journal of Medical Genetics. 45(5). 552–557. 27 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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