Conrad Gilliam

1.3k total citations
14 papers, 540 citations indexed

About

Conrad Gilliam is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Conrad Gilliam has authored 14 papers receiving a total of 540 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Conrad Gilliam's work include Heavy Metal Exposure and Toxicity (2 papers), Genetic Associations and Epidemiology (2 papers) and Drug Transport and Resistance Mechanisms (2 papers). Conrad Gilliam is often cited by papers focused on Heavy Metal Exposure and Toxicity (2 papers), Genetic Associations and Epidemiology (2 papers) and Drug Transport and Resistance Mechanisms (2 papers). Conrad Gilliam collaborates with scholars based in United States, United Kingdom and Venezuela. Conrad Gilliam's co-authors include Svetlana Lutsenko, Jack H. Kaplan, Konstantin Petrukhin, Matthew J. Cooper, Milton J. Finegold, Scott M. Vanderwerf, Clinton T. Morgan, Dominik Hüster, Jason L. Burkhead and Randal R. Nixon and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Neurology.

In The Last Decade

Conrad Gilliam

14 papers receiving 523 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Conrad Gilliam United States	9	325	184	168	146	77	14	540
Bryan Hall United States	5	470 1.4×	246 1.3×	217 1.3×	128 0.9×	94 1.2×	9	669
Jennifer A. Paynter Australia	7	628 1.9×	268 1.5×	310 1.8×	153 1.0×	46 0.6×	9	749
Benjamin P. Weaver United States	10	372 1.1×	196 1.1×	232 1.4×	39 0.3×	22 0.3×	16	574
Dustin Thomas United States	12	190 0.6×	238 1.3×	104 0.6×	119 0.8×	12 0.2×	15	607
Scott D. Dwyer United States	7	124 0.4×	160 0.9×	123 0.7×	32 0.2×	13 0.2×	7	371
Matthew J. Cooper United States	6	362 1.1×	162 0.9×	171 1.0×	187 1.3×	5 0.1×	7	496
Shuichi Hiyamuta Japan	8	339 1.0×	174 0.9×	89 0.5×	24 0.2×	8 0.1×	13	544
Fumiko Hara Japan	11	68 0.2×	159 0.9×	50 0.3×	37 0.3×	44 0.6×	29	334
Il‐Ha Lee Australia	9	115 0.4×	240 1.3×	36 0.2×	28 0.2×	24 0.3×	12	378
Isabelle Valnot France	8	108 0.3×	1.0k 5.6×	37 0.2×	21 0.1×	33 0.4×	10	1.1k

Countries citing papers authored by Conrad Gilliam

Since Specialization

Citations

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

Fields of papers citing papers by Conrad Gilliam

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Conrad Gilliam

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

All Works

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14 of 14 papers shown

Gilliam, Conrad, et al.. (2019). Molecular Interaction Network Approach (MINA) identifies association of novel candidate disease genes. MethodsX. 6. 1286–1291. 2 indexed citations

Gilliam, Conrad, et al.. (2018). Identification of novel susceptibility genes associated with seven autoimmune disorders using whole genome molecular interaction networks. Journal of Autoimmunity. 97. 48–58. 11 indexed citations

Xie, Bingqing, Gady Agam, Natalia Maltsev, & Conrad Gilliam. (2013). Conditional Random Field for Candidate Gene Prioritization. 700–701. 2 indexed citations

Cheng, Rong, Suh‐Hang Hank Juo, Jianjun Liu, et al.. (2010). Fine mapping of candidate regions for bipolar disorder provides strong evidence for susceptibility loci on chromosomes 7q. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(2). 168–176. 4 indexed citations

Hüster, Dominik, Milton J. Finegold, Clinton T. Morgan, et al.. (2006). Consequences of Copper Accumulation in the Livers of the Atp7b−/− (Wilson Disease Gene) Knockout Mice. American Journal Of Pathology. 168(2). 423–434. 176 indexed citations

Parano, Enrico, et al.. (2001). Noninvasive prenatal diagnosis of chromosomal aneuploidies by isolation and analysis of fetal cells from maternal blood. American Journal of Medical Genetics. 101(3). 262–267. 16 indexed citations

Gécz, Jozef, Shaun Barnett, Jianjun Liu, et al.. (1999). Characterization of the Human Glutamate Receptor Subunit 3 Gene (GRIA3), a Candidate for Bipolar Disorder and Nonspecific X-Linked Mental Retardation. Genomics. 62(3). 356–368. 73 indexed citations

Wilson, Matthew H., Ram S. Puranam, Ruth Ottman, et al.. (1998). Evaluation of the α _2A -adrenergic receptor gene in a heritable form of temporal lobe epilepsy. Neurology. 51(6). 1730–1731. 8 indexed citations

Lutsenko, Svetlana, Konstantin Petrukhin, Matthew J. Cooper, Conrad Gilliam, & Jack H. Kaplan. (1997). N-terminal Domains of Human Copper-transporting Adenosine Triphosphatases (the Wilson's and Menkes Disease Proteins) Bind Copper Selectively in Vivo and in Vitro with Stoichiometry of One Copper Per Metal-binding Repeat. Journal of Biological Chemistry. 272(30). 18939–18944. 189 indexed citations

10.

Youngman, S, Mansoor Sarfarazi, Maja Bućan, et al.. (1989). A new DNA marker (D4S90) is located terminally on the short arm of chromosome 4, close to the Huntington disease gene. Genomics. 5(4). 802–809. 25 indexed citations

11.

Murray, Jeffrey C., Kenneth H. Buetow, Mark A. Smith, et al.. (1988). Pairwise linkage analysis of 11 loci on human chromosome 4.. PubMed. 42(3). 490–7. 17 indexed citations

12.

Blanché, Hélène, Renata Žunec, Conrad Gilliam, et al.. (1987). A human anonymous low copy number clone, 4c11 (D6S4), localized to 6p12-6p21, detects 2 RFLPs, one of which is moderately polymorphic. Nucleic Acids Research. 15(14). 5902–5902. 4 indexed citations

13.

Scambler, Peter, Timothy P. Robbins, Conrad Gilliam, et al.. (1985). Linkage studies between polymorphic markers on chromosome 4 and cystic fibrosis. Human Genetics. 69(3). 250–254. 11 indexed citations

14.

Williamson, R., Kay E. Davies, Jennifer A. Donald, et al.. (1984). The implications of genetic variation in human pathology.. PubMed. 49. 183–8. 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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