Elizabeth A. Geiger

3.4k citations

20 papers · 1.2k indexed · h-index 16

Co-authors: Elizabeth Goldmuntz D. Woodrow Benson Tamim H. Shaikh Joshua J. Blinder Doff B. McElhinney Elaine H. Zackai Anita M. Quintana Hung‐Chun Yu
Topics: Genomic variations and chromosomal abnormalities (12 papers)Congenital heart defects research (8 papers)Chromosomal and Genetic Variations (7 papers)
Cited by: Genetics Molecular Biology Clinical Biochemistry
Journals: Circulation Journal of the American College of Cardiology Genetics
Partner nations: United States Canada Belgium

In The Last Decade

Elizabeth A. Geiger

20 papers receiving 1.2k citations

Peers

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

#	Work	Indexed citations
1	Genomic regions associated with microdeletion/microduplication syndromes exhibit extreme diversity of structural variation 2021 ·Genetics ·Yulia Mostovoy,Feyza Yilmaz,(unknown),Catherine Chu,Chin Jia Lin,Elizabeth A. Geiger,Naomi Meeks,Kathryn C. Chatfield,Curtis R. Coughlin,Urvashi Surti,Pui–Yan Kwok,Tamim H. Shaikh	13
2	The 22q11 low copy repeats are characterized by unprecedented size and structural variability 2019 ·Genome Research ·(unknown),Yulia Mostovoy,Feyza Yilmaz,(unknown),Steven Pastor,Matthew S. Hestand,Ann Swillen,Elfi Vergaelen,Elizabeth A. Geiger,Curtis R. Coughlin,(unknown),Donna M. McDonald‐McGinn,Bernice E. Morrow,Pui–Yan Kwok,Ming Xiao,Beverly S. Emanuel,Tamim H. Shaikh,Joris Vermeesch	28
3	Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalities 2017 ·Human Molecular Genetics ·Anita M. Quintana,Hung‐Chun Yu,(unknown),Mihaela Pupavac,Elizabeth A. Geiger,(unknown),(unknown),Warren Cheung,Shu‐Huang Chen,David Watkins,Tomi Pastinen,Flemming Skovby,Bruce Appel,David S. Rosenblatt,Tamim H. Shaikh	36
4	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 2016 ·Molecular Case Studies ·Hung‐Chun Yu,Curtis R. Coughlin,Elizabeth A. Geiger,(unknown),Ellen Roy Elias,Jean Cavanaugh,Kathryn C. Chatfield,Shelley D. Miyamoto,Tamim H. Shaikh	15
5	Kabuki syndrome genesKMT2DandKDM6A: functional analyses demonstrate critical roles in craniofacial, heart and brain development 2015 ·Human Molecular Genetics ·(unknown),Leif R. Neitzel,Anita M. Quintana,Elizabeth A. Geiger,Elaine H. Zackai,David E. Clouthier,Kristin Artinger,Jeffrey E. Ming,Tamim H. Shaikh	128
6	Mutations in the mitochondrial cysteinyl-tRNA synthase gene, CARS2, lead to a severe epileptic encephalopathy and complex movement disorder 2015 ·Journal of Medical Genetics ·Curtis R. Coughlin,Gunter Scharer,Marisa W. Friederich,Hung‐Chun Yu,Elizabeth A. Geiger,Geralyn Creadon‐Swindell,(unknown),Arnaud Vanlander,Rudy Van Coster,Christopher A. Powell,Michael A. Swanson,Michal Minczuk,Johan L.K. Van Hove,Tamim H. Shaikh	55
7	Hcfc1b, a zebrafish ortholog of HCFC1, regulates craniofacial development by modulating mmachc expression 2014 ·Developmental Biology ·Anita M. Quintana,Elizabeth A. Geiger,(unknown),David S. Rosenblatt,Kenneth N. Maclean,Sally P. Stabler,Kristin Artinger,Bruce Appel,Tamim H. Shaikh	33
8	An individual with blepharophimosis–ptosis–epicanthus inversus syndrome (BPES) and additional features expands the phenotype associated with mutations in KAT6B 2014 ·American Journal of Medical Genetics Part A ·Hung‐Chun Yu,Elizabeth A. Geiger,Līvija Medne,Elaine H. Zackai,Tamim H. Shaikh	30
9	An X-Linked Cobalamin Disorder Caused by Mutations in Transcriptional Coregulator HCFC1 2013 ·The American Journal of Human Genetics ·Hung‐Chun Yu,Jennifer L. Sloan,Gunter Scharer,(unknown),Anita M. Quintana,Nathan P. Achilly,Irini Manoli,Curtis R. Coughlin,Elizabeth A. Geiger,(unknown),David Watkins,Terttu Suormala,Johan L.K. Van Hove,Brian Fowler,Matthias R. Baumgartner,David S. Rosenblatt,Charles P. Venditti,Tamim H. Shaikh	90
10	Genes and biological processes commonly disrupted in rare and heterogeneous developmental delay syndromes 2010 ·Human Molecular Genetics ·Tamim H. Shaikh,Chad Haldeman‐Englert,Elizabeth A. Geiger,Chris P. Ponting,Caleb Webber	20
11	Recurrent interstitial 1p36 deletions: Evidence for germline mosaicism and complex rearrangement breakpoints 2010 ·American Journal of Medical Genetics Part A ·Marzena Gajęcka,Sulagna C. Saitta,Andrew J. Gentles,Lindsey Campbell,Karen L. Ciprero,Elizabeth A. Geiger,(unknown),Jill A. Rosenfeld,Tamim H. Shaikh,Lisa G. Shaffer	36
12	A 781‐kb deletion of 13q12.3 in a patient with Peters plus syndrome 2009 ·American Journal of Medical Genetics Part A ·Chad Haldeman‐Englert,(unknown),Elizabeth A. Geiger,(unknown),Holly Feret,(unknown),(unknown),Matthew A. Deardorff,Elaine H. Zackai,Tamim H. Shaikh	15
13	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 2009 ·American Journal of Medical Genetics Part A ·Chad Haldeman‐Englert,Kimberly A. Chapman,(unknown),Elizabeth A. Geiger,Donna M. McDonald‐McGinn,Eric Rappaport,Elaine H. Zackai,Nancy B. Spinner,Tamim H. Shaikh	27
14	A 3.1-Mb microdeletion of 3p21.31 associated with cortical blindness, cleft lip, CNS abnormalities, and developmental delay 2008 ·European Journal of Medical Genetics ·Chad Haldeman‐Englert,Xiaowu Gai,Juan C. Perín,(unknown),Sara Halbach,Elizabeth A. Geiger,Donna M. McDonald‐McGinn,Håkon Håkonarson,Elaine H. Zackai,Tamim H. Shaikh	15
15	Low copy repeats mediate distal chromosome 22q11.2 deletions: Sequence analysis predicts breakpoint mechanisms 2007 ·Genome Research ·Tamim H. Shaikh,(unknown),Mary Ella Pierpont,James McGrath,April M. Hacker,Manjunath Nimmakayalu,Elizabeth A. Geiger,Beverly S. Emanuel,Sulagna C. Saitta	94
16	Rapid detection of submicroscopic chromosomal rearrangements in children with multiple congenital anomalies using high density oligonucleotide arrays 2006 ·Human Mutation ·Jeffrey E. Ming,Elizabeth A. Geiger,(unknown),Karen L. Ciprero,Manjunath Nimmakayalu,Yi Zhang,Andrew T. Huang,(unknown),Eric Rappaport,Elaine H. Zackai,Tamim H. Shaikh	33
17	A patient with mosaic partial trisomy 18 resulting from dicentric chromosome breakage 2005 ·American Journal of Medical Genetics Part A ·Jennifer J.D. Morrissette,Līvija Medne,(unknown),(unknown),Elizabeth A. Geiger,Mary Pipan,Elaine H. Zackai,Tamim H. Shaikh,Nancy B. Spinner	6
18	NKX2.5mutations in patients with congenital heart disease 2003 ·Journal of the American College of Cardiology ·Doff B. McElhinney,Elizabeth A. Geiger,Joshua J. Blinder,D. Woodrow Benson,Elizabeth Goldmuntz	274
19	NKX2.5 Mutations in Patients With Tetralogy of Fallot 2001 ·Circulation ·Elizabeth Goldmuntz,Elizabeth A. Geiger,D. Woodrow Benson	246
20	A gene belonging to the Sm family of snRNP core proteins maps within the mouse MHC 1997 ·Immunogenetics ·Vahe Bedian,(unknown),Elizabeth A. Geiger,L. Charles Bailey,David L. Gasser	3

About Elizabeth A. Geiger

Elizabeth A. Geiger is a scholar working on Genetics, Clinical Biochemistry and Genetics, having authored 20 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Congenital heart defects research (8 papers) and Chromosomal and Genetic Variations (7 papers). The work is most often cited by research in Genetics (473 citations), Molecular Biology (963 citations) and Clinical Biochemistry (84 citations). Elizabeth A. Geiger has collaborated with scholars based in United States, Canada and Belgium. Frequent co-authors include Elizabeth Goldmuntz, D. Woodrow Benson, Tamim H. Shaikh, Joshua J. Blinder, D. Woodrow Benson, Doff B. McElhinney, Elaine H. Zackai, Anita M. Quintana, Hung‐Chun Yu and Kristin Artinger. Their work appears in journals such as Circulation, Journal of the American College of Cardiology and Genetics.

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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