Andrew J. Sharp

13.8k citations

103 papers · 6.7k · 2 hit papers · h-index 39

Impact in

Genetics top 0.2%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Molecular Biology top 2%
- Epigenetics and DNA Methylation
- Congenital heart defects research
- Genomics and Phylogenetic Studies

Papers in

Genetics 60
- Genomic variations and chromosomal abnormalities 32
- Genetic Syndromes and Imprinting 14
- Genetic Associations and Epidemiology 11
- Genetics and Neurodevelopmental Disorders 9
Molecular Biology 53
- Epigenetics and DNA Methylation 20
- Congenital heart defects research 11
- Genomics and Phylogenetic Studies 10

Co-authors: Evan E. Eichler (11 shared papers)Ze Cheng (5 shared papers)Daniel Pinkel (4 shared papers)Donna G. Albertson (4 shared papers)Paras Garg (18 shared papers)David Robinson (3 shared papers)Patricia A. Jacobs (3 shared papers)L.M. Pertz (2 shared papers)
Journals: Human Genetics (7 papers)Human Mutation (7 papers)PLoS Genetics (7 papers)Human Molecular Genetics (6 papers)The American Journal of Human Genetics (6 papers)
Partner nations: United States United Kingdom Switzerland

In The Last Decade

Andrew J. Sharp

101 papers receiving 6.5k citations

Andrew J. Sharp's Hit Papers

align trajectories log scale

Fine-scale structural variation of the human genome 2005 · 744 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2005 Nature Genetics
2005 The American Journal of Human Genetics

Peers

Countries citing papers authored by Andrew J. Sharp

Since Specialization

Citations

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

Fields of papers citing papers by Andrew J. Sharp

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Andrew J. Sharp, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Andrew J. Sharp Line = papers co-authored together Andrew J. Sharp links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 103 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Fine-scale structural variation of the human genome Nature Genetics ·Eray Tüzün, Andrew J. Sharp, Jeffrey A. Bailey, Rajinder Kaul, Victoria Morrison, L.M. Pertz, Eric Haugen, Hillary S. Hayden, Donna G. Albertson, Daniel Pinkel, Maynard V. Olson, Evan E. Eichler Hit paper breakdown →	2005	744
2	Segmental Duplications and Copy-Number Variation in the Human Genome The American Journal of Human Genetics ·Andrew J. Sharp, Devin P. Locke, Sean McGrath, Ze Cheng, Jeffrey A. Bailey, Rhea U. Vallente, L.M. Pertz, Royden A. Clark, Stuart Schwartz, Rick Segraves, Vanessa V. Oseroff, Donna G. Albertson, Daniel Pinkel, Evan E. Eichler Hit paper breakdown →	2005	682
3	Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome Nature Genetics ·Andrew J. Sharp, S.K. Hansen, Rebecca R. Selzer, Ze Cheng, Regina Regan, Jane A. Hurst, Helen Stewart, Sue Price, Edward Blair, Raoul C. M. Hennekam, Carrie Fitzpatrick, Rick Segraves, Todd Richmond, Cheryl Guiver, Donna G. Albertson, Daniel Pinkel, Peggy S. Eis, Stuart Schwartz, Samantha J.L. Knight, Evan E. Eichler	2006	428
4	Age- and tissue-specific variation of X chromosome inactivation ratios in normal women Human Genetics ·Andrew J. Sharp, David Robinson, Patricia A. Jacobs	2000	296
5	Abundant contribution of short tandem repeats to gene expression variation in humans Nature Genetics ·Melissa Gymrek, Thomas Willems, Audrey Guilmatre, Haoyang Zeng, Barak Markus, Stoyan Georgiev, Mark J. Daly, Alkes L. Price, Jonathan K. Pritchard, Andrew J. Sharp, Yaniv Erlich	2015	249
6	Linkage Disequilibrium and Heritability of Copy-Number Polymorphisms within Duplicated Regions of the Human Genome The American Journal of Human Genetics ·Devin P. Locke, Andrew J. Sharp, Steven A. McCarroll, Sean McGrath, Tera L. Newman, Ze Cheng, Stuart Schwartz, Donna G. Albertson, Daniel Pinkel, David Altshuler, Evan E. Eichler	2006	232
7	DNA methylation profiles of human active and inactive X chromosomes Genome Research ·Andrew J. Sharp, Elisavet Stathaki, Eugenia Migliavacca, Manisha Brahmachary, Stephen B. Montgomery, Yann Dupré, Stylianos E. Antonarakis	2011	220
8	Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant Journal of Medical Genetics ·Femke Hannes, Andrew J. Sharp, Heather C. Mefford, Thomy de Ravel, Claudia Ruivenkamp, M.H. Breuning, JP Fryns, Koenraad Devriendt, Griet Van Buggenhout, Annick Vogels, Helen Stewart, Raoul C. M. Hennekam, Gregory M. Cooper, Regina Regan, Samantha J.L. Knight, Evan E. Eichler, Joris Vermeesch	2008	209
9	Epigenome-wide differences in pathology-free regions of multiple sclerosis–affected brains Nature Neuroscience ·Jimmy Huynh, Paras Garg, Tin Htwe Thin, Seungyeul Yoo, Ranjan Dutta, Bruce D. Trapp, Vahram Haroutunian, Jun Zhu, Michael Donovan, Andrew J. Sharp, Patrizia Casaccia	2013	188
10	Recurrent Reciprocal Genomic Rearrangements of 17q12 Are Associated with Renal Disease, Diabetes, and Epilepsy The American Journal of Human Genetics ·Heather C. Mefford, Séverine Clauin, Andrew J. Sharp, Rikke S. Møller, Reinhard Ullmann, Raj P. Kapur, Dan Pinkel, Gregory M. Cooper, Mario Ventura, Hans‐Hilger Ropers, Niels Tommerup, Evan E. Eichler, Christine Bellanné‐Chantelot	2007	186
11	Structural Variation of the Human Genome Annual Review of Genomics and Human Genetics ·Andrew J. Sharp, Ze Cheng, Evan E. Eichler	2006	180
12	Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling down syndrome Mammalian Genome ·Arnaud Duchon, Matthieu Raveau, Claire Chevalier, Valérie Nalesso, Andrew J. Sharp, Yann Hérault	2011	172
13	Genome-wide DNA methylation profiling in the superior temporal gyrus reveals epigenetic signatures associated with Alzheimer’s disease Genome Medicine ·Corey T. Watson, Panos Roussos, Paras Garg, Daniel Ho, Nidha Azam, Pavel Katsel, Vahram Haroutunian, Andrew J. Sharp	2016	148
14	Genome-Wide DNA Methylation Profiling Reveals Epigenetic Changes in the Rat Nucleus Accumbens Associated With Cross-Generational Effects of Adolescent THC Exposure Neuropsychopharmacology ·Corey T. Watson, Henrietta Szutorisz, Paras Garg, Qammarah Martin, Joseph A. Landry, Andrew J. Sharp, Yasmin L. Hurd	2015	132
15	Characterization of a recurrent 15q24 microdeletion syndrome Human Molecular Genetics ·Andrew J. Sharp, Rebecca R. Selzer, Joris A. Veltman, Stefania Gimelli, Giorgio Gimelli, Pasquale Striano, Antonietta Coppola, Regina Regan, Sue Price, Nine V.A.M. Knoers, Peggy S. Eis, Han G. Brunner, Raoul C. M. Hennekam, Samantha J.L. Knight, Bert B.A. de Vries, Orsetta Zuffardi, Evan E. Eichler	2007	129
16	The Genetics of Microdeletion and Microduplication Syndromes: An Update Annual Review of Genomics and Human Genetics ·Corey T. Watson, (unknown), Andrew J. Sharp, Heather C. Mefford	2014	126
17	Xp deletions associated with autism in three females Human Genetics ·N. Simon Thomas, Andrew J. Sharp, C.E. Browne, David Skuse, Chris Hardie, Nicholas R. Dennis	1999	125
18	Polymorphic tandem repeats within gene promoters act as modifiers of gene expression and DNA methylation in humans Nucleic Acids Research ·Javier Quilez, Audrey Guilmatre, Paras Garg, Gareth Highnam, Melissa Gymrek, Yaniv Erlich, Ricky S. Joshi, David Mittelman, Andrew J. Sharp	2016	105
19	DNA Methylation Signatures of Early Childhood Malnutrition Associated With Impairments in Attention and Cognition Biological Psychiatry ·Cyril Peter, Laura Fischer, Marija Kundaković, Paras Garg, Mira Jakovcevski, Aslihan Dincer, Ana C. Amaral, Edward I. Ginns, Marzena Galdzicka, Cyralene P. Bryce, Chana Ratner, Deborah P. Waber, David J. Mokler, Gayle Medford, Frances A. Champagne, Douglas L. Rosene, Jill McGaughy, Andrew J. Sharp, Janina R. Galler, Schahram Akbarian	2016	103
20	Dynamics of DNA Methylation in Recent Human and Great Ape Evolution PLoS Genetics ·Irene Hernando-Herraez, Javier Prado-Martinez, Paras Garg, Marcos Fernández-Callejo, Holger Heyn, Christina Hvilsom, Arcadi Navarro, Manel Esteller, Andrew J. Sharp, Tomàs Marquès‐Bonet	2013	93

About Andrew J. Sharp

Andrew J. Sharp is a scholar working on Genetics, Molecular Biology, Plant Science, Pediatrics, Perinatology and Child Health and Ecology, Evolution, Behavior and Systematics, having authored 103 papers that have together received 6.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (32 papers), Epigenetics and DNA Methylation (20 papers), Chromosomal and Genetic Variations (20 papers), Genetic Syndromes and Imprinting (14 papers), Congenital heart defects research (11 papers), Genetic Associations and Epidemiology (11 papers), Genomics and Phylogenetic Studies (10 papers) and Genetics and Neurodevelopmental Disorders (9 papers). The work is most often cited by research in Genetics (3.7k citations), Molecular Biology (3.2k citations), Pediatrics, Perinatology and Child Health (722 citations), Plant Science (1.1k citations) and Cancer Research (360 citations). Andrew J. Sharp has collaborated with scholars based in United States, United Kingdom and Switzerland. Frequent co-authors include Evan E. Eichler, Ze Cheng, Daniel Pinkel, Donna G. Albertson, Paras Garg, David Robinson, Patricia A. Jacobs, L.M. Pertz, Jeffrey A. Bailey and Corey T. Watson. Their work appears in journals such as Human Genetics, Human Mutation, PLoS Genetics, Human Molecular Genetics and The American Journal of Human 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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Andrew J. Sharp

Andrew J. Sharp's Hit Papers

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All Works

About Andrew J. Sharp

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