Lisa G. Shaffer

30.3k citations

288 papers · 13.4k indexed · h-index 67

Genetics top 0.02%
Molecular Biology top 0.5%
Pediatrics, Perinatology and Child Health top 0.05%
Plant Science top 0.5%
Surgery top 5%

Co-authors: Blake C. Ballif Bassem A. Bejjani Jill A. Rosenfeld James R. Lupski Catherine D. Kashork Justine Coppinger Beth S. Torchia Frank Greenberg
Topics: Genomic variations and chromosomal abnormalities (190 papers)Prenatal Screening and Diagnostics (99 papers)Chromosomal and Genetic Variations (74 papers)
Cited by: Genetics Pediatrics, Perinatology and Child Health Molecular Biology
Journals: New England Journal of Medicine Proceedings of the National Academy of Sciences The Lancet
Partner nations: United States Canada United Kingdom

In The Last Decade

Lisa G. Shaffer

286 papers receiving 12.6k citations

Peers

Countries citing papers authored by Lisa G. Shaffer

Since Specialization

Citations

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

Fields of papers citing papers by Lisa G. Shaffer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lisa G. Shaffer. 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 Lisa G. Shaffer. The network helps show where Lisa G. Shaffer may publish in the future.

Co-authorship network of co-authors of Lisa G. Shaffer

This figure shows the co-authorship network connecting the top 25 collaborators of Lisa G. Shaffer. A scholar is included among the top collaborators of Lisa G. Shaffer 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 Lisa G. Shaffer. Lisa G. Shaffer 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	Chromosome Abnormalities and Genetic Counseling 2011 ·Oxford University Press eBooks ·R. J. M. Gardner,Grant R. Sutherland,Lisa G. Shaffer	335
2	Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems 2011 ·Genetics in Medicine ·Trilochan Sahoo,Aaron Theisen,Jill A. Rosenfeld,Allen N. Lamb,J. Britt Ravnan,Roger A. Schultz,Beth S. Torchia,Nicholas J. Neill,Ian Casci,Bassem A. Bejjani,Lisa G. Shaffer	75
3	Microdeletion 20p12.3 involving BMP2 contributes to syndromic forms of cleft palate 2011 ·American Journal of Medical Genetics Part A ·Trilochan Sahoo,Aaron Theisen,Pedro A. Sanchez‐Lara,Michael Marble,(unknown),Beth S. Torchia,Allen N. Lamb,Bassem A. Bejjani,Lisa G. Shaffer,Yves Lacassie	53
4	Comparative analysis of copy number detection by whole-genome BAC and oligonucleotide array CGH 2010 ·Molecular Cytogenetics ·Nicholas J. Neill,Beth S. Torchia,Bassem A. Bejjani,Lisa G. Shaffer,Blake C. Ballif	48
5	Whole‐genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray 2009 ·Prenatal Diagnosis ·Justine Coppinger,Sarah Alliman,Allen N. Lamb,Beth S. Torchia,Bassem A. Bejjani,Lisa G. Shaffer	97
6	Neuroimaging findings in children with rare or novel de novo chromosomal anomalies 2008 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Leon G. Epstein,Ali Jalali,(unknown),(unknown),Joshua V. Ross,Justine Coppinger,Katrin M. Carlson,Joel Charrow,Barbara K. Burton,Donald Zimmerman,John S. Curran,(unknown),(unknown),Delilah Burrowes,Brad Angle,Cynthia V. Stack,Lisa G. Shaffer,John A. Kessler,Alexander G. Bassuk	1
7	Development of a high-density pericentromeric region BAC clone set for the detection and characterization of small supernumerary marker chromosomes by array CGH 2007 ·Genetics in Medicine ·Blake C. Ballif,(unknown),(unknown),(unknown),(unknown),Emily A. Rorem,Aaron Theisen,Bassem A. Bejjani,Lisa G. Shaffer	46
8	Use of targeted array‐based CGH for the clinical diagnosis of chromosomal imbalance: Is less more? 2005 ·American Journal of Medical Genetics Part A ·Bassem A. Bejjani,Reza Saleki,Blake C. Ballif,Emily A. Rorem,Kyle Sundin,Aaron Theisen,Catherine D. Kashork,Lisa G. Shaffer	155
9	Microduplication and Triplication of 22q11.2: A Highly Variable Syndrome 2005 ·The American Journal of Human Genetics ·(unknown),Martin J. Somerville,Lionel Willatt,Helen V. Firth,Karen J. Harrison,Jennifer MacKenzie,(unknown),Bernice E. Morrow,Lisa G. Shaffer,Melanie Babcock,Judy Chernos,François P. Bernier,(unknown),(unknown),(unknown),(unknown),Margaret Lilley,(unknown),Heather E. McDermid	170
10	Delineation of mechanisms and regions of dosage imbalance in complex rearrangements of 1p36 leads to a putative gene for regulation of cranial suture closure 2004 ·European Journal of Human Genetics ·Marzena Gajęcka,Wei Yu,Blake C. Ballif,Caron D. Glotzbach,(unknown),Chad A. Shaw,Catherine D. Kashork,Heidi A. Heilstedt,(unknown),Aaron Theisen,Ritva Rice,David Rice,Lisa G. Shaffer	68
11	Omphalocele in trisomy 3q: further delineation of phenotype 2003 ·Clinical Genetics ·Svetlana A. Yatsenko,Roberto Mendoza‐Londono,John W. Belmont,Lisa G. Shaffer	20
12	Genome Architecture Catalyzes Nonrecurrent Chromosomal Rearrangements 2003 ·The American Journal of Human Genetics ·Paweł Stankiewicz,Christine J. Shaw,Jason Dapper,Keiko Wakui,Lisa G. Shaffer,Marjorie Withers,Leah I. Elizondo,Sung Sup Park,James R. Lupski	144
13	Obligate Short-Arm Exchange in De Novo Robertsonian Translocation Formation Influences Placement of Crossovers in Chromosome 21 Nondisjunction 2003 ·The American Journal of Human Genetics ·Sue Ann Berend,Scott L. Page,William Walker Atkinson,Christopher McCaskill,Neil E. Lamb,Stephanie L. Sherman,Lisa G. Shaffer	7
14	Robertsonian Translocations: Mechanisms of Formation, Aneuploidy, and Uniparental Disomy and Diagnostic Considerations 2002 ·Genetic Testing ·Sung‐Ryul Kim,Lisa G. Shaffer	45
15	Parental Origin and Timing of De Novo Robertsonian Translocation Formation 2002 ·The American Journal of Human Genetics ·(unknown),Anita Heller,(unknown),Christopher McCaskill,Sue Ann Berend,Scott L. Page,Lisa G. Shaffer	67
16	Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski−/− mice 2001 ·Nature Genetics ·Clemencia Colmenares,Heidi A. Heilstedt,Lisa G. Shaffer,Stuart Schwartz,Michael Berk,Jeffrey C. Murray,Ed Stavnezer	102
17	Haploinsufficiency of ALX4 as a Potential Cause of Parietal Foramina in the 11p11.2 Contiguous Gene–Deletion Syndrome 2000 ·The American Journal of Human Genetics ·Yuanqing Wu,José L. Badano,Christopher McCaskill,Hannes Vogel,Lorraine Potocki,Lisa G. Shaffer	65
18	A case of Williams syndrome with a large, visible cytogenetic deletion 1999 ·Journal of Medical Genetics ·Yuanqing Wu,Elizabeth Nickerson,Lisa G. Shaffer,Kim M. Keppler‐Noreuil,Ann Muilenburg	15
19	A Common Breakpoint on 11q23 in Carriers of the Constitutional t(11;22) Translocation 1999 ·The American Journal of Human Genetics ·Lisa Edelmann,Elizabeth Spiteri,(unknown),Rosalie Goldberg,Raj K. Pandita,Scott Duong,Joyce E. Fox,(unknown),Seema R. Lalani,Lisa G. Shaffer,Bernice E. Morrow	46
20	Very low maternal serum chorionic gonadotropin levels in association with fetal triploidy 1994 ·American Journal of Obstetrics and Gynecology ·(unknown),Lisa G. Shaffer,(unknown),(unknown),Frank Greenberg	0

About Lisa G. Shaffer

Lisa G. Shaffer is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Plant Science, having authored 288 papers that have together received 13.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (190 papers), Prenatal Screening and Diagnostics (99 papers) and Chromosomal and Genetic Variations (74 papers). The work is most often cited by research in Genetics (9.6k citations), Pediatrics, Perinatology and Child Health (4.2k citations) and Molecular Biology (6.1k citations). Lisa G. Shaffer has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Blake C. Ballif, Bassem A. Bejjani, Jill A. Rosenfeld, James R. Lupski, Catherine D. Kashork, Justine Coppinger, Beth S. Torchia, Frank Greenberg, Christopher McCaskill and Grant R. Sutherland. Their work appears in journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and The Lancet.

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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