George E. Houck

1.2k total citations
26 papers, 909 citations indexed

About

George E. Houck is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, George E. Houck has authored 26 papers receiving a total of 909 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 12 papers in Molecular Biology and 10 papers in Cognitive Neuroscience. Recurrent topics in George E. Houck's work include Genomic variations and chromosomal abnormalities (16 papers), Genetics and Neurodevelopmental Disorders (13 papers) and Autism Spectrum Disorder Research (10 papers). George E. Houck is often cited by papers focused on Genomic variations and chromosomal abnormalities (16 papers), Genetics and Neurodevelopmental Disorders (13 papers) and Autism Spectrum Disorder Research (10 papers). George E. Houck collaborates with scholars based in United States, Poland and Denmark. George E. Houck's co-authors include Sarah L. Nolin, Anne Glicksman, Carl Dobkin, W. Ted Brown, W. Ted Brown, W. Ted Brown, Fred J. Kieras, Karen Brøndum‐Nielsen, Elke Holinski‐Feder and Jean‐Louis Mandel and has published in prestigious journals such as Nucleic Acids Research, Annals of Neurology and Biochemical and Biophysical Research Communications.

In The Last Decade

George E. Houck

26 papers receiving 888 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
George E. Houck United States 14 752 456 447 66 62 26 909
Marie‐Françoise Croquette France 7 714 0.9× 327 0.7× 464 1.0× 79 1.2× 38 0.6× 11 842
Ravinesh A. Kumar United States 10 508 0.7× 278 0.6× 364 0.8× 73 1.1× 83 1.3× 16 767
Laura B. K. Herzing United States 12 482 0.6× 182 0.4× 442 1.0× 102 1.5× 33 0.5× 13 793
Seungtai Yoon United States 10 1.0k 1.4× 433 0.9× 821 1.8× 41 0.6× 67 1.1× 16 1.5k
Kristin Herman United States 7 371 0.5× 266 0.6× 270 0.6× 48 0.7× 63 1.0× 12 599
Amy K. Sullivan United States 7 756 1.0× 463 1.0× 352 0.8× 77 1.2× 56 0.9× 8 894
Linda S. Weaving Australia 9 619 0.8× 262 0.6× 428 1.0× 18 0.3× 44 0.7× 10 771
James Macpherson United Kingdom 11 570 0.8× 328 0.7× 303 0.7× 32 0.5× 71 1.1× 17 677
Sarah L. Nolin United States 21 1.4k 1.9× 927 2.0× 833 1.9× 83 1.3× 135 2.2× 44 1.6k
Hayley Archer United Kingdom 14 1.0k 1.4× 407 0.9× 558 1.2× 30 0.5× 69 1.1× 17 1.1k

Countries citing papers authored by George E. Houck

Since Specialization
Citations

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

Fields of papers citing papers by George E. Houck

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by George E. Houck. 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 George E. Houck. The network helps show where George E. Houck may publish in the future.

Co-authorship network of co-authors of George E. Houck

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

All Works

20 of 20 papers shown
1.
Nolin, Sarah L., Xiaohua Ding, George E. Houck, W. Ted Brown, & Carl Dobkin. (2007). Fragile X full mutation alleles composed of few alleles: Implications for CGG repeat expansion. American Journal of Medical Genetics Part A. 146A(1). 60–65. 18 indexed citations
2.
Nolin, Sarah L., W. Ted Brown, Anne Glicksman, et al.. (2003). Expansion of the Fragile X CGG Repeat in Females with Premutation or Intermediate Alleles. The American Journal of Human Genetics. 72(2). 454–464. 276 indexed citations
3.
Dobkin, Carl, et al.. (1999). Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detection. American Journal of Medical Genetics. 83(4). 338–341. 6 indexed citations
4.
Nolin, Sarah L., et al.. (1999). FMR1 CGG-Repeat Instability in Single Sperm and Lymphocytes of Fragile-X Premutation Males. The American Journal of Human Genetics. 65(3). 680–688. 30 indexed citations
5.
Jenkins, Edmund C., G. Y. Wen, Kwang Soo Kim, et al.. (1999). Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodies. American Journal of Medical Genetics. 83(4). 342–346. 7 indexed citations
6.
Brown, W. Ted, Sarah L. Nolin, George E. Houck, et al.. (1996). Prenatal diagnosis and carrier screening for fragile X by PCR. American Journal of Medical Genetics. 64(1). 191–195. 54 indexed citations
7.
Brown, W. Ted, Sarah L. Nolin, George E. Houck, et al.. (1996). Prenatal diagnosis and carrier screening for fragile X by PCR. American Journal of Medical Genetics. 64(1). 191–195. 5 indexed citations
8.
Nolin, Sarah L., F A Lewis, George E. Houck, et al.. (1996). Familial transmission of the FMR1 CGG repeat.. PubMed. 59(6). 1252–61. 146 indexed citations
9.
Zhong, Nan, et al.. (1994). Distribution of FMR‐1 and associated microsatellite alleles in a normal Chinese population. American Journal of Medical Genetics. 51(4). 417–422. 41 indexed citations
10.
Nolin, Sarah L., Anne Glicksman, George E. Houck, W. Ted Brown, & Carl Dobkin. (1994). Mosaicism in fragile X affected males. American Journal of Medical Genetics. 51(4). 509–512. 127 indexed citations
11.
Brown, W. Ted, George E. Houck, Xiaohua Ding, et al.. (1994). Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test. Obstetrical & Gynecological Survey. 49(4). 236–237. 7 indexed citations
12.
Jenkins, Edmund C., et al.. (1994). Fragile X induction systems in CVS cultures: Effect on cytogenetic, PCR, and genomic southern blot DNA analyses of the FMR‐1 gene. American Journal of Medical Genetics. 51(4). 436–442. 2 indexed citations
13.
Houck, George E., et al.. (1993). Cytogenetic and molecular identification of a de novo direct duplication of the long arm of chromosome 4(q21.3→q31.3). American Journal of Medical Genetics. 46(1). 83–87. 26 indexed citations
14.
Houck, George E., et al.. (1992). Reassessment of a chromosome 12q + marker by fluorescent in situ hybridization (FISH). Clinical Genetics. 42(3). 124–128. 4 indexed citations
15.
Nolin, Sarah L., Edmund C. Jenkins, Michael S. Krawczun, et al.. (1991). Fragile X screening program in New York State. American Journal of Medical Genetics. 38(2-3). 251–255. 29 indexed citations
16.
Jenkins, Edmund C., Nikolaos K. Robakis, W. Ted Brown, et al.. (1988). Fine mapping of an Alzheimer Disease-associated gene encoding beta-amyloid protein. Biochemical and Biophysical Research Communications. 151(1). 1–8. 14 indexed citations
17.
Kieras, Fred J., et al.. (1986). Elevation of urinary hyaluronic acid in Werner's syndrome and progeria. Biochemical Medicine and Metabolic Biology. 36(3). 276–282. 15 indexed citations
18.
Brown, W. Ted, et al.. (1985). Molecular Quantitation of Aneuploid Conditions Using Chromosome 21 as a Model. Annals of the New York Academy of Sciences. 450(1). 85–94. 4 indexed citations
19.
Wisniewski, Krystyna E., et al.. (1984). Ultrastructural, neurological, and glycosaminoglycan abnormalities in Lowe's syndrome. Annals of Neurology. 16(1). 40–49. 6 indexed citations
20.
Kieras, Fred J., George E. Houck, Joseph H. French, & Krystyna E. Wisniewski. (1984). Low sulfated glycosaminoglycans are excreted in patients with the Lowe syndrome. Biochemical Medicine. 31(2). 201–210. 14 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Marie‐Françoise Croquette Breakdown of academic impact, for papers by Ravinesh A. Kumar Breakdown of academic impact, for papers by Laura B. K. Herzing Breakdown of academic impact, for papers by Seungtai Yoon Breakdown of academic impact, for papers by Kristin Herman Breakdown of academic impact, for papers by Amy K. Sullivan Breakdown of academic impact, for papers by Linda S. Weaving Breakdown of academic impact, for papers by James Macpherson Breakdown of academic impact, for papers by Sarah L. Nolin Breakdown of academic impact, for papers by Hayley Archer
Rankless by CCL
2026