Arthur Grix

1.8k total citations
13 papers, 820 citations indexed

About

Arthur Grix is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Arthur Grix has authored 13 papers receiving a total of 820 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Arthur Grix's work include Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (2 papers) and RNA modifications and cancer (2 papers). Arthur Grix is often cited by papers focused on Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (2 papers) and RNA modifications and cancer (2 papers). Arthur Grix collaborates with scholars based in United States, Türkiye and Jordan. Arthur Grix's co-authors include Virginia V. Michels, Roberta A Pagon, Dawna Armstrong, Renata Laxová, John M. Opitz, Cynthia J. Curry, Frank Greenberg, Lewis B. Holmes, Meinhard Robinow and James F. Reynolds and has published in prestigious journals such as Nature Genetics, Human Molecular Genetics and Muscle & Nerve.

In The Last Decade

Arthur Grix

13 papers receiving 798 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Arthur Grix United States 10 476 161 154 138 126 13 820
Nouriya Al‐Sannaa Saudi Arabia 13 290 0.6× 99 0.6× 150 1.0× 64 0.5× 67 0.5× 27 611
Lakshmi Mehta United States 16 403 0.8× 59 0.4× 348 2.3× 86 0.6× 96 0.8× 46 754
Thorsten Rosenbaum Germany 19 237 0.5× 167 1.0× 98 0.6× 63 0.5× 62 0.5× 39 899
Christine Wittevrongel Belgium 18 241 0.5× 262 1.6× 175 1.1× 38 0.3× 72 0.6× 36 882
Rıza Köksal Özgül Türkiye 17 457 1.0× 77 0.5× 194 1.3× 43 0.3× 37 0.3× 69 873
Leena Peltonen Finland 8 295 0.6× 78 0.5× 311 2.0× 39 0.3× 49 0.4× 9 935
Ali‐Reza Moslemi Sweden 20 956 2.0× 162 1.0× 132 0.9× 21 0.2× 61 0.5× 40 1.2k
Hagit Baris Israel 17 385 0.8× 69 0.4× 203 1.3× 83 0.6× 74 0.6× 49 965
Yumiko Okubo Japan 10 336 0.7× 83 0.5× 135 0.9× 50 0.4× 77 0.6× 27 791
Motomichi Kosuga Japan 19 239 0.5× 179 1.1× 157 1.0× 62 0.4× 83 0.7× 54 839

Countries citing papers authored by Arthur Grix

Since Specialization
Citations

This map shows the geographic impact of Arthur 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 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 Grix more than expected).

Fields of papers citing papers by Arthur Grix

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arthur Grix

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

All Works

13 of 13 papers shown
1.
Stolle, Catherine A., et al.. (2010). Clinical and functional properties of novel VHL mutation (X214L) consistent with Type 2A phenotype and low risk of renal cell carcinoma. Clinical Genetics. 79(6). 539–545. 9 indexed citations
2.
Shen, Jun, Edward C. Gilmore, Mary Haddadin, et al.. (2010). Mutations in PNKP cause microcephaly, seizures and defects in DNA repair. Nature Genetics. 42(3). 245–249. 213 indexed citations
3.
4.
McGahan, John P., Arthur Grix, & Eugenio O. Gerscovich. (1994). Prenatal diagnosis of lissencephaly: Miller‐Dieker syndrome. Journal of Clinical Ultrasound. 22(9). 560–563. 15 indexed citations
5.
Reichel, Martin, Arthur Grix, & R. Rivkah Isseroff. (1992). Dyskeratosis Congenita Associated with Elevated Fetal Hemoglobin, X‐Linked Ocular Albinism, and Juvenile‐Onset Diabetes Mellitus. Pediatric Dermatology. 9(2). 103–106. 14 indexed citations
6.
Tuttle, Deborah, et al.. (1992). Interstitial deletion of the short arm of chromosome 1 (46XY), del(1)(p13p22.3). American Journal of Medical Genetics. 44(5). 551–554. 12 indexed citations
7.
Gronert, Gerald A., William M. Fowler, George H. Cardinet, et al.. (1992). Absence of malignant hyperthermia contractures in Becker‐Duchenne dystrophy at age 2. Muscle & Nerve. 15(1). 52–56. 12 indexed citations
8.
Kang, Seok Seon, et al.. (1991). Intermediate hyperhomocysteinemia resulting from compound heterozygosity of methylenetetrahydrofolate reductase mutations.. PubMed. 48(3). 546–51. 107 indexed citations
9.
Dobyns, William B., Roberta A Pagon, Dawna Armstrong, et al.. (1989). Diagnostic criteria for Walker‐Warburg syndrome. American Journal of Medical Genetics. 32(2). 195–210. 313 indexed citations
10.
Gorczyca, David P., John P. McGahan, Karen K. Lindfors, William G. Ellis, & Arthur Grix. (1989). Arthrogryposis multiplex congenita: Prenatal ultrasonographic diagnosis. Journal of Clinical Ultrasound. 17(1). 40–44. 11 indexed citations
11.
Hecht, Frederick, Arthur Grix, Barbara K. Hecht, et al.. (1984). Direct prenatal chromosome diagnosis of a malignancy. Cancer Genetics and Cytogenetics. 11(1). 107–111. 29 indexed citations
12.
Grix, Arthur, et al.. (1979). Noonan phenotype with polydactyly.. PubMed. 15(5B). 313–9. 3 indexed citations
13.
Grix, Arthur & Samuel T. Giammona. (1974). Pneumonitis with pleural effusion in children due to Mycoplasma pneumoniae.. PubMed. 109(6). 665–71. 8 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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