Nancy J. Carpenter

4.1k total citations · 1 hit paper
72 papers, 2.2k citations indexed

About

Nancy J. Carpenter is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Nancy J. Carpenter has authored 72 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Genetics, 27 papers in Molecular Biology and 13 papers in Cognitive Neuroscience. Recurrent topics in Nancy J. Carpenter's work include Genetics and Neurodevelopmental Disorders (32 papers), Genomic variations and chromosomal abnormalities (20 papers) and Autism Spectrum Disorder Research (13 papers). Nancy J. Carpenter is often cited by papers focused on Genetics and Neurodevelopmental Disorders (32 papers), Genomic variations and chromosomal abnormalities (20 papers) and Autism Spectrum Disorder Research (13 papers). Nancy J. Carpenter collaborates with scholars based in United States, Canada and United Kingdom. Nancy J. Carpenter's co-authors include Zilong Sun, Carolin Däumer, Julie R. Korenberg, Rivkah Gonsky, Christine M. Distèche, Peter St. J. Dignan, Burhan Say, Richard J. Simensen, Jeanette J. A. Holden and Gene S. Fisch and has published in prestigious journals such as Proceedings of the National Academy of Sciences, American Journal of Psychiatry and Genetics.

In The Last Decade

Nancy J. Carpenter

68 papers receiving 2.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Down syndrome phenotypes: the consequences of chromosomal imbalance.

1994 556 citations Nancy J. Carpenter et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nancy J. Carpenter United States	24	1.2k	1.0k	325	321	292	72	2.2k
Christophe Philippe France	30	1.6k 1.3×	1.5k 1.5×	309 1.0×	190 0.6×	207 0.7×	77	2.7k
J Boué France	22	1.5k 1.2×	1.4k 1.4×	583 1.8×	103 0.3×	377 1.3×	82	2.6k
Beverly J. White United States	26	935 0.8×	660 0.6×	132 0.4×	324 1.0×	294 1.0×	61	1.9k
Aravinda Chakravarti United States	18	1.0k 0.8×	671 0.7×	395 1.2×	184 0.6×	243 0.8×	30	1.9k
Petter Strømme Norway	28	1.1k 0.9×	1.2k 1.1×	311 1.0×	111 0.3×	296 1.0×	76	2.7k
Sylvain Briault France	23	1.6k 1.3×	1.8k 1.8×	610 1.9×	93 0.3×	248 0.8×	64	3.1k
M. W. Partington Canada	33	2.0k 1.6×	1.8k 1.7×	506 1.6×	97 0.3×	314 1.1×	110	3.5k
Françoise Muscatelli France	31	2.2k 1.8×	2.7k 2.6×	180 0.6×	178 0.6×	322 1.1×	65	4.4k
John Dean United Kingdom	30	1.4k 1.1×	1.3k 1.2×	267 0.8×	307 1.0×	575 2.0×	103	3.5k
Armin Schumacher United States	21	785 0.6×	2.4k 2.3×	174 0.5×	174 0.5×	140 0.5×	47	3.5k

Countries citing papers authored by Nancy J. Carpenter

Since Specialization

Citations

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

Fields of papers citing papers by Nancy J. Carpenter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nancy J. Carpenter

This figure shows the co-authorship network connecting the top 25 collaborators of Nancy J. Carpenter. A scholar is included among the top collaborators of Nancy J. Carpenter 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 Nancy J. Carpenter. Nancy J. Carpenter 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

Fisch, Gene S., Nancy J. Carpenter, Patricia N. Howard‐Peebles, et al.. (2007). Studies of age‐correlated features of cognitive‐behavioral development in children and adolescents with genetic disorders. American Journal of Medical Genetics Part A. 143A(20). 2478–2489. 39 indexed citations

Carpenter, Nancy J.. (2001). Molecular cytogenetics. Seminars in Pediatric Neurology. 8(3). 135–146. 15 indexed citations

Crawford, Dana C., Charles E. Schwartz, Kellen L. Meadows, et al.. (2000). Survey of the Fragile X Syndrome CGG Repeat and the Short-Tandem-Repeat and Single-Nucleotide-Polymorphism Haplotypes in an African American Population. The American Journal of Human Genetics. 66(2). 480–493. 44 indexed citations

Fisch, Gene S., Nancy J. Carpenter, Jeanette J. A. Holden, et al.. (1999). Longitudinal assessment of adaptive and maladaptive behaviors in fragile X males: Growth, development, and profiles. American Journal of Medical Genetics. 83(4). 257–263. 36 indexed citations

Carpenter, Nancy J., et al.. (1999). X-linked mental retardation syndrome with characteristic ?coarse? facial appearance, brachydactyly, and short stature maps to proximal Xq. American Journal of Medical Genetics. 85(3). 230–235. 6 indexed citations

Carpenter, Nancy J., et al.. (1999). Regional localization of a nonspecific X-linked mental retardation gene (MRX59) to Xp21.2-p22.2. American Journal of Medical Genetics. 85(3). 266–270. 13 indexed citations

Fisch, Gene S., Nancy J. Carpenter, Jeanette J. A. Holden, et al.. (1999). Longitudinal changes in cognitive and adaptive behavior in fragile X females: A prospective multicenter analysis. American Journal of Medical Genetics. 83(4). 308–312.

Fisch, Gene S., Richard J. Simensen, Jack Tarleton, et al.. (1996). Longitudinal study of cognitive abilities and adaptive behavior levels in fragile X males: A prospective multicenter analysis. American Journal of Medical Genetics. 64(2). 356–361. 67 indexed citations

Fisch, Gene S., Nancy J. Carpenter, Patricia N. Howard‐Peebles, et al.. (1996). Lack of association between mutation size and cognitive/behavior deficits in fragile X males: A brief report. American Journal of Medical Genetics. 64(2). 362–364. 8 indexed citations

10.

Macri, James N., Kenneth L. Garver, Philip D. Buchanan, et al.. (1994). Maternal serum free beta hCG screening: Results of studies including 480 cases of down syndrome. Prenatal Diagnosis. 14(2). 97–103. 47 indexed citations

11.

Fisch, Gene S., Jeanette J. A. Holden, Richard J. Simensen, et al.. (1994). Is fragile X syndrome a pervasive developmental disability? Cognitive ability and adaptive behavior in males with the full mutation. American Journal of Medical Genetics. 51(4). 346–352. 13 indexed citations

12.

Proud, Virginia K., Clive Levine, & Nancy J. Carpenter. (1992). New X‐linked syndrome with seizures, acquired micrencephaly, and agenesis of the corpus callosum. American Journal of Medical Genetics. 43(1-2). 458–466. 35 indexed citations

13.

Carpenter, Nancy J.. (1991). DNA linkage analysis of 26 families with fragile X syndrome. American Journal of Medical Genetics. 38(2-3). 311–318. 3 indexed citations

14.

Carpenter, Nancy J., Stephen N. Thibodeau, & W. Ted Brown. (1991). Linkage relationships between DXS105, DXS98, and other polymorphic DNA markers flanking the fragile X locus. American Journal of Medical Genetics. 38(2-3). 349–353. 4 indexed citations

15.

Smith, Barbara A., Douglas Skarecky, Ulla Bengtsson, et al.. (1988). Isolation of DNA markers in the direction of the Huntington disease gene from the G8 locus.. PubMed Central. 42(2). 335–44. 80 indexed citations

16.

Say, Burhan, Nancy J. Carpenter, John M. Opitz, & James F. Reynolds. (1988). Report of a case resembling the proteus syndrome with a chromosome abnormality. American Journal of Medical Genetics. 31(4). 987–989. 23 indexed citations

17.

Carpenter, Nancy J., et al.. (1988). Variable immunodeficiency with abnormal condensation of the heterochromatin of chromosomes 1, 9, and 16. The Journal of Pediatrics. 112(5). 757–760. 34 indexed citations

18.

Butler, Merlin G., Mark A. Fletcher, F. John Meaney, et al.. (1988). Metacarpophalangeal pattern profile analysis in fragile X syndrome. American Journal of Medical Genetics. 31(4). 767–773. 11 indexed citations

19.

Butler, Merlin G., et al.. (1988). Preliminary communication: Photoanthropometric analysis of individuals with the fragile X syndrome. American Journal of Medical Genetics. 30(1-2). 165–168. 15 indexed citations

20.

MacDonald, Marcy E., Mary Anne Anderson, T. Conrad Gilliam, et al.. (1987). A somatic cell hybrid panel for localizing DNA segments near the Huntington's disease gene. Genomics. 1(1). 29–34. 54 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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