Arnold Oliphant

21.7k total citations · 2 hit papers
38 papers, 4.5k citations indexed

About

Arnold Oliphant is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Arnold Oliphant has authored 38 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 14 papers in Genetics and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Arnold Oliphant's work include Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (6 papers) and RNA and protein synthesis mechanisms (6 papers). Arnold Oliphant is often cited by papers focused on Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (6 papers) and RNA and protein synthesis mechanisms (6 papers). Arnold Oliphant collaborates with scholars based in United States, Netherlands and United Kingdom. Arnold Oliphant's co-authors include Kevin Struhl, Ken Song, Craig A. Struble, David Barker, Mark S. Chee, Andrew B. Sparks, Christopher J. Brandl, Eric T. Wang, Mark H. Skolnick and Curtis L. Atkin and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Arnold Oliphant

38 papers receiving 4.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Identification of Mutations in the COL4A5 Collagen Gene in Alport Syndrome

1990 612 citations Arnold Oliphant, Curtis L. Atkin et al. profile →
Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18

2012 424 citations Mary E. Norton, Herb Brar et al. American Journal of Obstetrics and Gynecology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Arnold Oliphant United States	28	2.1k	1.5k	1.3k	708	388	38	4.5k
Heidi Stuhlmann United States	34	3.8k 1.8×	208 0.1×	1.3k 1.0×	906 1.3×	382 1.0×	71	7.1k
Richard Gelinas United States	35	4.5k 2.2×	261 0.2×	2.9k 2.3×	320 0.5×	591 1.5×	67	6.6k
Franck Letourneur France	35	1.2k 0.6×	277 0.2×	539 0.4×	458 0.6×	228 0.6×	96	3.9k
Edward R. LaVallie United States	32	3.0k 1.4×	215 0.1×	730 0.6×	122 0.2×	459 1.2×	54	5.3k
Antony C. Willis United Kingdom	31	1.5k 0.7×	515 0.3×	305 0.2×	113 0.2×	141 0.4×	46	3.8k
Christine A. Wells Australia	41	2.8k 1.3×	198 0.1×	539 0.4×	436 0.6×	422 1.1×	126	5.5k
Nada Jabado Canada	48	3.0k 1.5×	178 0.1×	757 0.6×	569 0.8×	881 2.3×	168	7.0k
M. van der Ploeg Netherlands	41	2.5k 1.2×	375 0.2×	1.4k 1.1×	158 0.2×	406 1.0×	102	4.9k
Geertruida M. Veldman United States	20	2.0k 1.0×	193 0.1×	951 0.7×	131 0.2×	286 0.7×	26	4.3k
Frans C.�S. Ramaekers Netherlands	33	2.0k 1.0×	177 0.1×	418 0.3×	313 0.4×	177 0.5×	87	4.1k

Countries citing papers authored by Arnold Oliphant

Since Specialization

Citations

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

Fields of papers citing papers by Arnold Oliphant

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arnold Oliphant

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

All Works

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20 of 20 papers shown

Huang, Stephanie, Kara Juneau, Patrick E. Bogard, et al.. (2016). Identifying Robertsonian Translocation Carriers by Microarray-Based DNA Analysis. Fetal Diagnosis and Therapy. 40(1). 59–62. 14 indexed citations

Juneau, Kara, Patrick E. Bogard, Stephanie Huang, et al.. (2014). Microarray-Based Cell-Free DNA Analysis Improves Noninvasive Prenatal Testing. Fetal Diagnosis and Therapy. 36(4). 282–286. 65 indexed citations

Wolfberg, Adam, Craig A. Struble, Jacob M. Zahn, et al.. (2014). Non‐invasive risk assessment of fetal sex chromosome aneuploidy through directed analysis and incorporation of fetal fraction. Prenatal Diagnosis. 34(5). 496–499. 43 indexed citations

Hidestrand, Mats, Karl Stamm, Aoy Tomita‐Mitchell, et al.. (2013). Quantification of Circulating Donor Specific Cell Free DNA Is an Exquisitely Sensitive Non-Invasive Indicator of Injury to the Donor Heart. The Journal of Heart and Lung Transplantation. 32(4). S101–S102. 1 indexed citations

Struble, Craig A., Argyro Syngelaki, Arnold Oliphant, Ken Song, & K. H. Nicolaides. (2013). Fetal Fraction Estimate in Twin Pregnancies Using Directed Cell-Free DNA Analysis. Fetal Diagnosis and Therapy. 35(3). 199–203. 39 indexed citations

Wang, Eric, Annette Batey, Craig A. Struble, et al.. (2013). Gestational age and maternal weight effects on fetal cell‐free DNA in maternal plasma. Prenatal Diagnosis. 33(7). 662–666. 302 indexed citations

Bonanno, Clarissa, et al.. (2013). Fraction of cell‐free fetal DNA in the maternal serum as a predictor of abnormal placental invasion‐a pilot study. Prenatal Diagnosis. 33(11). 1050–1053. 30 indexed citations

Sparks, Andrew B., Eric T. Wang, Craig A. Struble, et al.. (2012). Selective analysis of cell‐free DNA in maternal blood for evaluation of fetal trisomy. Prenatal Diagnosis. 32(1). 3–9. 208 indexed citations

Norton, Mary E., Herb Brar, Jonathan M. Weiss, et al.. (2012). Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18. American Journal of Obstetrics and Gynecology. 207(2). 137.e1–137.e8. 424 indexed citations breakdown →

10.

Hidestrand, Mats, Renee Stokowski, Ken Song, et al.. (2012). Influence of Temperature during Transportation on Cell-Free DNA Analysis. Fetal Diagnosis and Therapy. 31(2). 122–128. 57 indexed citations

11.

Sparks, Andrew B., Craig A. Struble, Eric T. Wang, Ken Song, & Arnold Oliphant. (2012). Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18. American Journal of Obstetrics and Gynecology. 206(4). 319.e1–319.e9. 322 indexed citations

12.

Gunderson, Kevin L., Frank J. Steemers, Pauline C. Ng, et al.. (2006). Whole‐Genome Genotyping. Methods in enzymology on CD-ROM/Methods in enzymology. 410. 359–376. 83 indexed citations

13.

Barker, David, Mark S. Hansen, A. Fawad Faruqi, et al.. (2004). Two Methods of Whole-Genome Amplification Enable Accurate Genotyping Across a 2320-SNP Linkage Panel. Genome Research. 14(5). 901–907. 176 indexed citations

14.

Gunderson, Kevin L., Semyon Kruglyak, Francisco García‐García, et al.. (2004). Decoding Randomly Ordered DNA Arrays. Genome Research. 14(5). 870–877. 222 indexed citations

15.

Fan, Jian‐Bing, Joanne M. Yeakley, Marina Bibikova, et al.. (2004). A Versatile Assay for High-Throughput Gene Expression Profiling on Universal Array Matrices. Genome Research. 14(5). 878–885. 148 indexed citations

16.

Murray, Sarah S., Arnold Oliphant, Richard Shen, et al.. (2004). A highly informative SNP linkage panel for human genetic studies. Nature Methods. 1(2). 113–117. 49 indexed citations

17.

Cole, B C, Kevin L. Knudtson, Arnold Oliphant, et al.. (1996). The sequence of the Mycoplasma arthritidis superantigen, MAM: identification of functional domains and comparison with microbial superantigens and plant lectin mitogens.. The Journal of Experimental Medicine. 183(3). 1105–1110. 44 indexed citations

18.

Oliphant, Arnold & Kevin Struhl. (1988). Defining the consensus sequences ofE.colipromoter elements by random selectio. Nucleic Acids Research. 16(15). 7673–7684. 53 indexed citations

19.

Hill, David E., Arnold Oliphant, & Kevin Struhl. (1987). [34] Mutagenesis with degenerate oligonucleotides: An efficient method for saturating a defined DNA region with base pair substitutions. Methods in enzymology on CD-ROM/Methods in enzymology. 155. 558–568. 46 indexed citations

20.

Oliphant, Arnold, et al.. (1974). Digital video: Error correcting codes and a practical study of a Wyner-Ash error corrector. NASA STI/Recon Technical Report N. 75. 15855. 3 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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