Andrew Kirby

19.9k total citations · 1 hit paper
29 papers, 3.2k citations indexed

About

Andrew Kirby is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Andrew Kirby has authored 29 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 10 papers in Molecular Biology and 3 papers in Plant Science. Recurrent topics in Andrew Kirby's work include Genetic Associations and Epidemiology (10 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genomics and Rare Diseases (6 papers). Andrew Kirby is often cited by papers focused on Genetic Associations and Epidemiology (10 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genomics and Rare Diseases (6 papers). Andrew Kirby collaborates with scholars based in United States, Canada and Australia. Andrew Kirby's co-authors include Mark J. Daly, Hyun Min Kang, David Heckerman, Eleazar Eskin, Noah Zaitlen, Claire M. Wade, John D. Rioux, Eric S. Lander, David A. van Heel and Sheila Fisher and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Andrew Kirby

29 papers receiving 3.2k 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.

Efficient Control of Population Structure in Model Organism Association Mapping

2008 1.3k citations Andrew Kirby, Mark J. Daly et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Andrew Kirby United States	23	1.9k	1.2k	719	339	203	29	3.2k
Joël Gellin France	26	2.4k 1.3×	1.7k 1.4×	857 1.2×	213 0.6×	157 0.8×	82	3.7k
Lluı́s Armengol Spain	24	1.4k 0.7×	1.2k 1.0×	433 0.6×	105 0.3×	142 0.7×	61	2.7k
Jeffrey G. Reid United States	21	1.1k 0.6×	1.7k 1.4×	329 0.5×	127 0.4×	233 1.1×	33	3.0k
Chris Cotsapas United States	23	2.3k 1.2×	1.5k 1.2×	179 0.2×	218 0.6×	385 1.9×	44	3.8k
Vincenzo Russo Italy	40	1.8k 0.9×	1.1k 0.9×	294 0.4×	454 1.3×	61 0.3×	172	4.3k
Anne E. Kwitek United States	34	1.5k 0.8×	2.0k 1.7×	229 0.3×	346 1.0×	383 1.9×	125	4.5k
Florian Guillou France	39	2.1k 1.1×	3.0k 2.5×	211 0.3×	400 1.2×	352 1.7×	116	5.8k
Mary Sara McPeek United States	24	1.7k 0.9×	800 0.7×	343 0.5×	90 0.3×	91 0.4×	52	2.5k
James Ireland United States	11	1.4k 0.7×	1.4k 1.2×	189 0.3×	106 0.3×	225 1.1×	13	2.8k
Luisa Dandolo France	29	1.7k 0.9×	3.7k 3.1×	190 0.3×	197 0.6×	163 0.8×	44	4.7k

Countries citing papers authored by Andrew Kirby

Since Specialization

Citations

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

Fields of papers citing papers by Andrew Kirby

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrew Kirby

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

20 of 20 papers shown

1.

Dauber, Andrew, Marina Cunha-Silva, Delanie B. Macedo, et al.. (2017). Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty. The Journal of Clinical Endocrinology & Metabolism. 102(5). 1557–1567. 142 indexed citations

2.

Hutchinson, John N., Jes Fagerness, Andrew Kirby, et al.. (2014). (Epi)Genetic Analyses of Age-Related Macular Degeneration: Case-Control and Discordant Twin Studies. Human Heredity. 78(2). 59–72. 11 indexed citations

3.

Pinto, Ricardo Mouro, Ella Dragileva, Andrew Kirby, et al.. (2013). Mismatch Repair Genes Mlh1 and Mlh3 Modify CAG Instability in Huntington's Disease Mice: Genome-Wide and Candidate Approaches. PLoS Genetics. 9(10). e1003930–e1003930. 155 indexed citations

4.

MacArthur, Daniel G., Andrew Kirby, Brett Thomas, et al.. (2013). Mutations ineIF4ENIF1Are Associated With Primary Ovarian Insufficiency. The Journal of Clinical Endocrinology & Metabolism. 98(9). E1534–E1539. 52 indexed citations

5.

Thompson, Benjamin R., et al.. (2012). Autosomal monoallelic expression in the mouse. Genome biology. 13(2). 85 indexed citations

6.

Haas, Joel T., Harland S. Winter, Elaine T. Lim, et al.. (2012). DGAT1 mutation is linked to a congenital diarrheal disorder. Journal of Clinical Investigation. 122(12). 4680–4684. 115 indexed citations

7.

Staropoli, John F., Amel Karaa, Elaine T. Lim, et al.. (2012). A Homozygous Mutation in KCTD7 Links Neuronal Ceroid Lipofuscinosis to the Ubiquitin-Proteasome System. The American Journal of Human Genetics. 91(1). 202–208. 84 indexed citations

8.

Talkowski, Michael E., Carl Ernst, Adrian Heilbut, et al.. (2011). Next-Generation Sequencing Strategies Enable Routine Detection of Balanced Chromosome Rearrangements for Clinical Diagnostics and Genetic Research. The American Journal of Human Genetics. 88(4). 469–481. 120 indexed citations

9.

Shao, Haifeng, Lindsay C. Burrage, David S. Sinasac, et al.. (2008). Genetic architecture of complex traits: Large phenotypic effects and pervasive epistasis. Proceedings of the National Academy of Sciences. 105(50). 19910–19914. 198 indexed citations

10.

Shen, Fan, Jing Huang, Karen Fitch, et al.. (2008). Improved detection of global copy number variation using high density, non-polymorphic oligonucleotide probes. BMC Genetics. 9(1). 27–27. 18 indexed citations

11.

Sissons, J. G. P., Bo‐Shiun Yan, Alexander Pichugin, et al.. (2008). Multigenic control of tuberculosis resistance: analysis of a QTL on mouse chromosome 7 and its synergism with sst1. Genes and Immunity. 10(1). 37–46. 22 indexed citations

12.

Tello-Ruiz, Marcela K, Terrye Delmonte, Cosmas Giallourakis, et al.. (2006). Haplotype-based association analysis of 56 functional candidate genes in the IBD6 locus on chromosome 19. European Journal of Human Genetics. 14(6). 780–790. 23 indexed citations

13.

Yan, Bo‐Shiun, Andrew Kirby, Yuriy V. Shebzukhov, Mark J. Daly, & Igor Kramnik. (2006). Genetic architecture of tuberculosis resistance in a mouse model of infection. Genes and Immunity. 7(3). 201–210. 42 indexed citations

14.

Heel, David A. van, Sheila Fisher, Andrew Kirby, et al.. (2004). Inflammatory bowel disease susceptibility loci defined by genome scan meta-analysis of 1952 affected relative pairs. Human Molecular Genetics. 13(7). 763–770. 184 indexed citations

15.

Pato, Carlos N., Michele T. Pato, Andrew Kirby, et al.. (2004). Genome‐wide scan in Portuguese Island families implicates multiple loci in bipolar disorder: Fine mapping adds support on chromosomes 6 and 11. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 127B(1). 30–34. 29 indexed citations

16.

Lindgren, Cecilia M., Melanie M. Mahtani, Elisabeth Widén, et al.. (2002). Genomewide Search for Type 2 Diabetes Mellitus Susceptibility Loci in Finnish Families: The Botnia Study. The American Journal of Human Genetics. 70(2). 509–516. 118 indexed citations

17.

Levinson, Douglas F., et al.. (2001). Simulation studies of detection of a complex disease in a partially isolated population. American Journal of Medical Genetics. 105(1). 65–70. 1 indexed citations

18.

Levinson, Douglas F., et al.. (2001). Simulation studies of detection of a complex disease in a partially isolated population. American Journal of Medical Genetics. 105(1). 65–70. 26 indexed citations

19.

Lehto, Markku, Melanie M. Mahtani, Elisabeth Widén, et al.. (1997). Characterization of the MODY3 phenotype. Early-onset diabetes caused by an insulin secretion defect.. Journal of Clinical Investigation. 99(4). 582–591. 168 indexed citations

20.

Daly, Mark J., Andrew Kirby, & Leonid Kruglyak. (1997). Do multiple data sets provide support for a bipolar illness susceptibility locus on chromosome 18?. Genetic Epidemiology. 14(6). 599–604. 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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