Andrew G. Hadd

4.6k citations

43 papers · 3.4k indexed · 1 hit paper · h-index 24

Genetics top 2%
- Genetics and Neurodevelopmental Disorders 18
- Genomic variations and chromosomal abnormalities 8
- Genomics and Rare Diseases 4
Cellular and Molecular Neuroscience top 2%
Cognitive Neuroscience top 2%
- Autism Spectrum Disorder Research 13
Molecular Biology top 5%
- RNA modifications and cancer 5
- RNA and protein synthesis mechanisms 5
Ecology top 2%
Cancer Research
- Cancer Genomics and Diagnostics 5
Biomedical Engineering
- Microfluidic and Capillary Electrophoresis Applications 4

Co-authors: Stevan Jovanovich J. Michael Ramsey Stephen C. Jacobson Gary J. Latham Oded Béjà Linh P. Nguyen Edward F. DeLong L. Aravind
Cited by: Genetics Cellular and Molecular Neuroscience Cognitive Neuroscience
Partner nations: United States Spain Italy

In The Last Decade

Andrew G. Hadd

41 papers receiving 3.3k citations

Hit Papers

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Peers

Countries citing papers authored by Andrew G. Hadd

Since Specialization

Citations

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

Fields of papers citing papers by Andrew G. Hadd

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Andrew G. Hadd, 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 G. Hadd Line = papers co-authored together Andrew G. Hadd links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Establishing a Common Lexicon for Circulating Tumor DNA Analysis and Molecular Residual Disease: Insights From the BLOODPAC Consortium Andrew G. Hadd,Angela Silvestro,Brittany A. McKelvey,Jonathan Baden,Christina Bormann Chung,Ben Brown,Fernando Cruz‐Guilloty,James H. Godsey,Gregory Jones,Chun‐Hui Lin,Dorys Lopez Ramos,Daniel Norton,Melanie R. Palomares,Carol E. Peña,Thereasa A. Rich,Ángel Luis Rodríguez,Mark Stewart,Diana Merino Vega,Lauren C. Leiman	2025	0
2	Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation alleles Sarah L. Nolin,Anne Glicksman,Nicole Tortora,Emily G. Allen,James Macpherson,Montserrat Milà,Angela Maria Vianna‐Morgante,Stephanie L. Sherman,Carl Dobkin,Gary J. Latham,Andrew G. Hadd	2019	47
3	Validation of Fragile X Screening in the Newborn Population Using a Fit-for-Purpose FMR1 PCR Assay System Stacey Lee,Jennifer Taylor,Charles Redmond,Andrew G. Hadd,Jon Kemppainen,Brian C. Haynes,Scott M. Shone,Donald B. Bailey,Gary J. Latham	2019	8
4	Absence of AGG Interruptions Is a Risk Factor for Full Mutation Expansion Among Israeli FMR1 Premutation Carriers Noam Domniz,Liat Ries‐Levavi,Yoram Cohen,Lilach Marom-Haham,Michal Berkenstadt,Elon Pras,Anne Glicksman,Nicole Tortora,Gary J. Latham,Andrew G. Hadd,Sarah L. Nolin,Shai E. Elizur	2018	13
5	Integration of Wet and Dry Bench Processes Optimizes Targeted Next-generation Sequencing of Low-quality and Low-quantity Tumor Biopsies Jeffrey Houghton,Andrew G. Hadd,R. Zeigler,Brian C. Haynes,Gary J. Latham	2016	2
6	A methylation PCR method determines FMR1 activation ratios and differentiates premutation allele mosaicism in carrier siblings Andrew G. Hadd,Stela Filipovic-Sadic,Lili Zhou,Arianna Williams,Gary J. Latham,Elizabeth Berry‐Kravis,Deborah J. Hall	2016	10
7	CGG allele size somatic mosaicism and methylation in FMR1 premutation alleles Dalyir Pretto,Guadalupe Mendoza‐Morales,Joyce Lo,Ru Cao,Andrew G. Hadd,Gary J. Latham,Blythe Durbin‐Johnson,Randi J. Hagerman,Flora Tassone	2014	66
8	Coevolution of Specificity Determinants in Eukaryotic Glutamyl- and Glutaminyl-tRNA Synthetases Andrew G. Hadd,John J. Perona	2014	14
9	Intermediate CGG repeat length at the FMR1 locus is not associated with hormonal indicators of ovarian age Jennie Kline,Ann M. Kinney,Bruce Levin,Stephen Brown,Andrew G. Hadd,Dorothy Warburton	2014	13
10	The role of AGG interruptions in fragile X repeat expansions: a twenty-year perspective Gary J. Latham,Justine Coppinger,Andrew G. Hadd,Sarah L. Nolin	2014	42
11	AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission Carolyn M. Yrigollen,Loreto Martorell,Blythe Durbin‐Johnson,Montserrat Naudó,Jordi Genovès,Alessandra Murgia,Roberta Polli,Lili Zhou,Deborah Barbouth,Abigail Rupchock,Brenda Finucane,Gary J. Latham,Andrew G. Hadd,Elizabeth Berry‐Kravis,Flora Tassone	2014	82
12	Fragile X AGG analysis provides new risk predictions for 45–69 repeat alleles Sarah L. Nolin,Sachin Sah,Anne Glicksman,Stephanie L. Sherman,Emily G. Allen,Elizabeth Berry‐Kravis,Flora Tassone,Carolyn M. Yrigollen,Amy Cronister,Marcia Jodah,Nicole Ersalesi,Carl Dobkin,W. Ted Brown,Raghav Shroff,Gary J. Latham,Andrew G. Hadd	2013	99
13	Targeted, High-Depth, Next-Generation Sequencing of Cancer Genes in Formalin-Fixed, Paraffin-Embedded and Fine-Needle Aspiration Tumor Specimens Andrew G. Hadd,Jeff Houghton,Ashish Choudhary,Sachin Sah,Liangjing Chen,Adam C. Marko,Tiffany Sanford,Kalyan Buddavarapu,Julie Krosting,Lana X. Garmire,Dennis Wylie,Rupali Shinde,Sylvie Beaudenon,Erik K. Alexander,Elizabeth Mambo,Alex Adai,Gary J. Latham	2013	141
14	Structural conservation of an ancient tRNA sensor in eukaryotic glutaminyl-tRNA synthetase Thomas D. Grant,Edward H. Snell,Joseph R. Luft,Erin Quartley,Stephanie Corretore,Jennifer R. Wolfley,M. Elizabeth Snell,Andrew G. Hadd,John J. Perona,Eric M. Phizicky,Elizabeth J. Grayhack	2011	14
15	High-resolution methylation polymerase chain reaction for fragile X analysis: Evidence for novel FMR1 methylation patterns undetected in Southern blot analyses Liangjing Chen,Andrew G. Hadd,Sachin Sah,Jeffrey Houghton,Stela Filipovic-Sadic,Wenting Zhang,Paul J. Hagerman,Flora Tassone,Gary J. Latham	2011	69
16	Adoption of array technologies into the clinical laboratory Andrew G. Hadd,Justin T. Brown,Bernard F. Andruss,Fei Ye,Cindy R WalkerPeach	2005	15
17	Microsphere Bead Arrays and Sequence Validation of 5/7/9T Genotypes for Multiplex Screening of Cystic Fibrosis Polymorphisms Andrew G. Hadd,Walairat Laosinchai-Wolf,Chris R. Novak,M. R. Badgett,Lesley A. Isgur,Marianna Goldrick,Cindy R WalkerPeach	2004	13
18	Bacterial Rhodopsin: Evidence for a New Type of Phototrophy in the Seabreakdown → Oded Béjà,L. Aravind,Eugene V. Koonin,Marcelino T. Suzuki,Andrew G. Hadd,Linh P. Nguyen,Stevan Jovanovich,Christian M. Gates,Robert A. Feldman,John L. Spudich,Elena N. Spudich,Edward F. DeLong	2000	1069
19	Sub-microliter DNA sequencing for capillary array electrophoresis Andrew G. Hadd,Michael J. Goard,David R. Rank,Stevan Jovanovich	2000	12
20	Kinetics and Mechanism of the Nucleophilic Substitution Reaction of Imidazole with Bis(2,4,6-trichlorophenyl) Oxalate and Bis(2,4-dinitrophenyl) Oxalate Andrew G. Hadd,John W. Birks	1996	26

About Andrew G. Hadd

Andrew G. Hadd is a scholar working on Genetics, Cognitive Neuroscience and Physical and Theoretical Chemistry, having authored 43 papers that have together received 3.4k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (18 papers), Autism Spectrum Disorder Research (13 papers), Genomic variations and chromosomal abnormalities (8 papers), RNA modifications and cancer (5 papers), Cancer Genomics and Diagnostics (5 papers), RNA and protein synthesis mechanisms (5 papers), Genomics and Rare Diseases (4 papers) and Microfluidic and Capillary Electrophoresis Applications (4 papers). The work is most often cited by research in Genetics (1.0k citations), Cellular and Molecular Neuroscience (679 citations) and Cognitive Neuroscience (715 citations). Andrew G. Hadd has collaborated with scholars based in United States, Spain and Italy. Frequent co-authors include Stevan Jovanovich, J. Michael Ramsey, Stephen C. Jacobson, Gary J. Latham, Oded Béjà, Linh P. Nguyen, Edward F. DeLong, L. Aravind, Marcelino T. Suzuki and Robert A. Feldman.

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