Elizabeth A. Geiger

3.4k total citations
20 papers, 1.2k citations indexed

About

Elizabeth A. Geiger is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Elizabeth A. Geiger has authored 20 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 13 papers in Genetics and 8 papers in Plant Science. Recurrent topics in Elizabeth A. Geiger's work include Genomic variations and chromosomal abnormalities (12 papers), Congenital heart defects research (8 papers) and Chromosomal and Genetic Variations (7 papers). Elizabeth A. Geiger is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Congenital heart defects research (8 papers) and Chromosomal and Genetic Variations (7 papers). Elizabeth A. Geiger collaborates with scholars based in United States, Canada and Belgium. Elizabeth A. Geiger's co-authors include Elizabeth Goldmuntz, D. Woodrow Benson, Tamim H. Shaikh, D. Woodrow Benson, Joshua J. Blinder, Doff B. McElhinney, Elaine H. Zackai, Anita M. Quintana, Hung‐Chun Yu and Kristin Artinger and has published in prestigious journals such as Circulation, Journal of the American College of Cardiology and Genetics.

In The Last Decade

Elizabeth A. Geiger

20 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elizabeth A. Geiger United States	16	963	473	393	178	112	20	1.2k
Jeroen Breckpot Belgium	19	562 0.6×	392 0.8×	221 0.6×	81 0.5×	96 0.9×	56	900
Maria Lisa Dentici Italy	19	704 0.7×	459 1.0×	139 0.4×	106 0.6×	61 0.5×	74	1.1k
Rossella Capolino Italy	18	449 0.5×	369 0.8×	146 0.4×	84 0.5×	72 0.6×	56	825
Boris Keren France	21	649 0.7×	515 1.1×	52 0.1×	39 0.2×	53 0.5×	70	1.1k
Pagon Ra United States	6	450 0.5×	260 0.5×	49 0.1×	38 0.2×	57 0.5×	291	791
Rannar Airik United States	21	1.3k 1.3×	445 0.9×	78 0.2×	181 1.0×	177 1.6×	32	1.5k
Ortal Barel Israel	15	450 0.5×	247 0.5×	57 0.1×	38 0.2×	68 0.6×	63	868
Michael Marble United States	13	370 0.4×	234 0.5×	65 0.2×	63 0.4×	21 0.2×	33	636
P. Gallano Spain	20	1.0k 1.0×	287 0.6×	39 0.1×	59 0.3×	261 2.3×	65	1.4k
Angus Dobbie United Kingdom	12	402 0.4×	284 0.6×	35 0.1×	57 0.3×	27 0.2×	20	675

Countries citing papers authored by Elizabeth A. Geiger

Since Specialization

Citations

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

Fields of papers citing papers by Elizabeth A. Geiger

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elizabeth A. Geiger. 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 Elizabeth A. Geiger. The network helps show where Elizabeth A. Geiger may publish in the future.

Co-authorship network of co-authors of Elizabeth A. Geiger

This figure shows the co-authorship network connecting the top 25 collaborators of Elizabeth A. Geiger. A scholar is included among the top collaborators of Elizabeth A. Geiger 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 Elizabeth A. Geiger. Elizabeth A. Geiger 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

Mostovoy, Yulia, Feyza Yilmaz, Catherine Chu, et al.. (2021). Genomic regions associated with microdeletion/microduplication syndromes exhibit extreme diversity of structural variation. Genetics. 217(2). 13 indexed citations

Mostovoy, Yulia, Feyza Yilmaz, Steven Pastor, et al.. (2019). The 22q11 low copy repeats are characterized by unprecedented size and structural variability. Genome Research. 29(9). 1389–1401. 28 indexed citations

Quintana, Anita M., Hung‐Chun Yu, Mihaela Pupavac, et al.. (2017). Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalities. Human Molecular Genetics. 26(15). 2838–2849. 36 indexed citations

Yu, Hung‐Chun, Curtis R. Coughlin, Elizabeth A. Geiger, et al.. (2016). Discovery of a potentially deleterious variant in TMEM87B in a patient with a hemizygous 2q13 microdeletion suggests a recessive condition characterized by congenital heart disease and restrictive cardiomyopathy. Molecular Case Studies. 2(3). a000844–a000844. 15 indexed citations

Neitzel, Leif R., Anita M. Quintana, Elizabeth A. Geiger, et al.. (2015). Kabuki syndrome genesKMT2DandKDM6A: functional analyses demonstrate critical roles in craniofacial, heart and brain development. Human Molecular Genetics. 24(15). 4443–4453. 128 indexed citations

Coughlin, Curtis R., Gunter Scharer, Marisa W. Friederich, et al.. (2015). Mutations in the mitochondrial cysteinyl-tRNA synthase gene, CARS2, lead to a severe epileptic encephalopathy and complex movement disorder. Journal of Medical Genetics. 52(8). 532–540. 55 indexed citations

Quintana, Anita M., Elizabeth A. Geiger, David S. Rosenblatt, et al.. (2014). Hcfc1b, a zebrafish ortholog of HCFC1, regulates craniofacial development by modulating mmachc expression. Developmental Biology. 396(1). 94–106. 33 indexed citations

Yu, Hung‐Chun, Elizabeth A. Geiger, Līvija Medne, Elaine H. Zackai, & Tamim H. Shaikh. (2014). An individual with blepharophimosis–ptosis–epicanthus inversus syndrome (BPES) and additional features expands the phenotype associated with mutations in KAT6B. American Journal of Medical Genetics Part A. 164(4). 950–957. 30 indexed citations

Yu, Hung‐Chun, Jennifer L. Sloan, Gunter Scharer, et al.. (2013). An X-Linked Cobalamin Disorder Caused by Mutations in Transcriptional Coregulator HCFC1. The American Journal of Human Genetics. 93(3). 506–514. 90 indexed citations

10.

Shaikh, Tamim H., Chad Haldeman‐Englert, Elizabeth A. Geiger, Chris P. Ponting, & Caleb Webber. (2010). Genes and biological processes commonly disrupted in rare and heterogeneous developmental delay syndromes. Human Molecular Genetics. 20(5). 880–893. 20 indexed citations

11.

Gajęcka, Marzena, Sulagna C. Saitta, Andrew J. Gentles, et al.. (2010). Recurrent interstitial 1p36 deletions: Evidence for germline mosaicism and complex rearrangement breakpoints. American Journal of Medical Genetics Part A. 152A(12). 3074–3083. 36 indexed citations

12.

Haldeman‐Englert, Chad, Kimberly A. Chapman, Elizabeth A. Geiger, et al.. (2009). A de novo 8.8‐Mb deletion of 21q21.1–q21.3 in an autistic male with a complex rearrangement involving chromosomes 6, 10, and 21. American Journal of Medical Genetics Part A. 152A(1). 196–202. 27 indexed citations

13.

Haldeman‐Englert, Chad, Elizabeth A. Geiger, Holly Feret, et al.. (2009). A 781‐kb deletion of 13q12.3 in a patient with Peters plus syndrome. American Journal of Medical Genetics Part A. 149A(8). 1842–1845. 15 indexed citations

14.

Haldeman‐Englert, Chad, Xiaowu Gai, Juan C. Perín, et al.. (2008). A 3.1-Mb microdeletion of 3p21.31 associated with cortical blindness, cleft lip, CNS abnormalities, and developmental delay. European Journal of Medical Genetics. 52(4). 265–268. 15 indexed citations

15.

Shaikh, Tamim H., Mary Ella Pierpont, James McGrath, et al.. (2007). Low copy repeats mediate distal chromosome 22q11.2 deletions: Sequence analysis predicts breakpoint mechanisms. Genome Research. 17(4). 482–491. 94 indexed citations

16.

Ming, Jeffrey E., Elizabeth A. Geiger, Karen L. Ciprero, et al.. (2006). Rapid detection of submicroscopic chromosomal rearrangements in children with multiple congenital anomalies using high density oligonucleotide arrays. Human Mutation. 27(5). 467–473. 33 indexed citations

17.

Morrissette, Jennifer J.D., Līvija Medne, Elizabeth A. Geiger, et al.. (2005). A patient with mosaic partial trisomy 18 resulting from dicentric chromosome breakage. American Journal of Medical Genetics Part A. 137A(2). 208–212. 6 indexed citations

18.

McElhinney, Doff B., Elizabeth A. Geiger, Joshua J. Blinder, D. Woodrow Benson, & Elizabeth Goldmuntz. (2003). NKX2.5mutations in patients with congenital heart disease. Journal of the American College of Cardiology. 42(9). 1650–1655. 274 indexed citations

19.

Goldmuntz, Elizabeth, Elizabeth A. Geiger, & D. Woodrow Benson. (2001). NKX2.5 Mutations in Patients With Tetralogy of Fallot. Circulation. 104(21). 2565–2568. 246 indexed citations

20.

Bedian, Vahe, et al.. (1997). A gene belonging to the Sm family of snRNP core proteins maps within the mouse MHC. Immunogenetics. 46(5). 427–430. 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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