Daniel A. Peiffer

2.8k total citations
19 papers, 926 citations indexed

About

Daniel A. Peiffer is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Daniel A. Peiffer has authored 19 papers receiving a total of 926 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Surgery. Recurrent topics in Daniel A. Peiffer's work include Genomic variations and chromosomal abnormalities (6 papers), Developmental Biology and Gene Regulation (5 papers) and Congenital heart defects research (4 papers). Daniel A. Peiffer is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Developmental Biology and Gene Regulation (5 papers) and Congenital heart defects research (4 papers). Daniel A. Peiffer collaborates with scholars based in United States, Japan and United Kingdom. Daniel A. Peiffer's co-authors include Kevin L. Gunderson, Sau Wai Cheung, Richard Shen, Weihua Chang, David Barker, Jennie Le, Frank J. Steemers, Jiangzhen Li, Chad A. Shaw and Francisco García‐García and has published in prestigious journals such as Development, Genome Research and Developmental Biology.

In The Last Decade

Daniel A. Peiffer

19 papers receiving 910 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daniel A. Peiffer United States 14 554 466 135 110 107 19 926
Ghazala Mirza United Kingdom 18 552 1.0× 714 1.5× 182 1.3× 47 0.4× 116 1.1× 20 1.1k
Shola M. Richards Switzerland 5 711 1.3× 929 2.0× 122 0.9× 102 0.9× 86 0.8× 5 1.3k
Bérengère de Martinville United States 17 616 1.1× 389 0.8× 69 0.5× 72 0.7× 94 0.9× 27 980
Christian Babbs United Kingdom 19 842 1.5× 444 1.0× 46 0.3× 88 0.8× 76 0.7× 35 1.2k
Debora Bogani United Kingdom 22 1.2k 2.2× 615 1.3× 58 0.4× 161 1.5× 57 0.5× 29 1.6k
Anne Harrington United States 13 1.1k 2.0× 289 0.6× 112 0.8× 74 0.7× 102 1.0× 20 1.5k
Martine Doco‐Fenzy France 15 349 0.6× 302 0.6× 59 0.4× 47 0.4× 70 0.7× 29 690
Gurbax S. Sekhon United States 17 596 1.1× 522 1.1× 86 0.6× 71 0.6× 124 1.2× 42 1.1k
E. Redeker Netherlands 17 571 1.0× 284 0.6× 48 0.4× 48 0.4× 91 0.9× 29 808
Beth A. Firulli United States 20 1.1k 1.9× 283 0.6× 99 0.7× 151 1.4× 36 0.3× 34 1.2k

Countries citing papers authored by Daniel A. Peiffer

Since Specialization
Citations

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

Fields of papers citing papers by Daniel A. Peiffer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniel A. Peiffer

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel A. Peiffer. A scholar is included among the top collaborators of Daniel A. Peiffer 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 Daniel A. Peiffer. Daniel A. Peiffer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Lai, Lisa A., Rumen Kostadinov, Michael T. Barrett, et al.. (2010). Deletion at Fragile Sites Is a Common and Early Event in Barrett's Esophagus. Molecular Cancer Research. 8(8). 1084–1094. 36 indexed citations
2.
Peiffer, Daniel A. & Kevin L. Gunderson. (2009). Design of Tag SNP Whole Genome Genotyping Arrays. Methods in molecular biology. 529. 51–61. 8 indexed citations
3.
Li, Xiaohong, Patricia C. Galipeau, Carissa A. Sanchez, et al.. (2008). Single Nucleotide Polymorphism–Based Genome-Wide Chromosome Copy Change, Loss of Heterozygosity, and Aneuploidy in Barrett's Esophagus Neoplastic Progression. Cancer Prevention Research. 1(6). 413–423. 55 indexed citations
4.
Chen, Jing, Liping Guo, Daniel A. Peiffer, et al.. (2008). Genomic profiling of 766 cancer‐related genes in archived esophageal normal and carcinoma tissues. International Journal of Cancer. 122(10). 2249–2254. 49 indexed citations
5.
Simovich, Marcia J., Daniel A. Peiffer, Kevin L. Gunderson, et al.. (2008). Delineation of the proximal 3q microdeletion syndrome. American Journal of Medical Genetics Part A. 146A(13). 1729–1735. 14 indexed citations
6.
Lennon, Patrick A., M. Lance Cooper, Daniel A. Peiffer, et al.. (2007). Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: Clinical report and review. American Journal of Medical Genetics Part A. 143A(8). 791–798. 62 indexed citations
7.
Eberle, Michael A., Pauline C. Ng, Kenneth Kuhn, et al.. (2007). Power to Detect Risk Alleles Using Genome-Wide Tag SNP Panels. PLoS Genetics. 3(10). e170–e170. 74 indexed citations
8.
Powis, Zöe, Sung‐Hae Kang, M. Lance Cooper, et al.. (2007). Mosaic tetrasomy 12p with triplication of 12p detected by array‐based comparative genomic hybridization of peripheral blood DNA. American Journal of Medical Genetics Part A. 143A(24). 2910–2915. 15 indexed citations
9.
Peiffer, Daniel A., Jennie Le, Frank J. Steemers, et al.. (2006). High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping. Genome Research. 16(9). 1136–1148. 373 indexed citations
10.
Blitz, Ira L., Daniel A. Peiffer, Ying Wáng, et al.. (2006). Schnurri transcription factors fromDrosophilaand vertebrates can mediate Bmp signaling through a phylogenetically conserved mechanism. Development. 133(20). 4025–4034. 50 indexed citations
11.
Peiffer, Daniel A. & Kevin L. Gunderson. (2006). SNP-CGH technologies for genomic profiling of LOH and copy number. 3 indexed citations
12.
Bubnoff, Andreas von, Daniel A. Peiffer, Ira L. Blitz, et al.. (2005). Phylogenetic footprinting and genome scanning identify vertebrate BMP response elements and new target genes. Developmental Biology. 281(2). 210–226. 56 indexed citations
13.
Baldessari, Danila, Yongchol Shin, Olga Krebs, et al.. (2005). Global gene expression profiling and cluster analysis in Xenopus laevis. Mechanisms of Development. 122(3). 441–475. 49 indexed citations
14.
Eberle, Michael A., Kenneth Kuhn, Daniel A. Peiffer, et al.. (2005). Power to Detect Risk Alleles Using Genome-Wide Tag SNP Panels. PLoS Genetics. preprint(2007). e170–e170. 1 indexed citations
15.
Shin, Yongchul, Atsushi Kitayama, Tetsuya Koide, et al.. (2005). Identification of neural genes using Xenopus DNA microarrays. Developmental Dynamics. 233(1). 248–248. 3 indexed citations
16.
Peiffer, Daniel A., Andreas von Bubnoff, Yongchol Shin, et al.. (2004). A Xenopus DNA microarray approach to identify novel direct BMP target genes involved in early embryonic development. Developmental Dynamics. 232(2). 445–456. 24 indexed citations
17.
Shin, Yongchol, Atsushi Kitayama, Tetsuya Koide, et al.. (2004). Identification of neural genes using Xenopus DNA microarrays. Developmental Dynamics. 232(2). 432–444. 28 indexed citations
18.
Peiffer, Daniel A., Ken Cho, & Yongchol Shin. (2003). Xenopus DNA Microarrays. Current Genomics. 4(8). 665–672. 6 indexed citations
19.
Birch, Helen L., Thomas J. Smith, Colin Poulton, Daniel A. Peiffer, & Allen E. Goodship. (2002). Do regional variations in flexor tendons predispose to site‐specific injuries?. Equine Veterinary Journal. 34(S34). 288–292. 20 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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