Bernice A. Allitto

2.1k total citations · 1 hit paper
22 papers, 1.4k citations indexed

About

Bernice A. Allitto is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Bernice A. Allitto has authored 22 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 7 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Bernice A. Allitto's work include Genetic Neurodegenerative Diseases (8 papers), Cystic Fibrosis Research Advances (7 papers) and DNA Repair Mechanisms (4 papers). Bernice A. Allitto is often cited by papers focused on Genetic Neurodegenerative Diseases (8 papers), Cystic Fibrosis Research Advances (7 papers) and DNA Repair Mechanisms (4 papers). Bernice A. Allitto collaborates with scholars based in United States, United Kingdom and Italy. Bernice A. Allitto's co-authors include Elaine A. Sugarman, Elizabeth M. Rohlfs, Zhaoqing Zhou, Viatcheslav R. Akmaev, Thomas Scholl, Kerry L. Flynn, Narasimhan Nagan, Brant C. Hendrickson, Hui Zhu and Ruth A. Heim and has published in prestigious journals such as Science, Nucleic Acids Research and Journal of Clinical Investigation.

In The Last Decade

Bernice A. Allitto

20 papers receiving 1.3k 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.

Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72 400 specimens

2011 457 citations Elaine A. Sugarman, Narasimhan Nagan et al. European Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bernice A. Allitto United States	15	782	497	307	307	305	22	1.4k
Siu‐Li Yong Canada	11	353 0.5×	523 1.1×	420 1.4×	437 1.4×	61 0.2×	12	1.2k
Hubert Journel France	23	563 0.7×	77 0.2×	128 0.4×	229 0.7×	99 0.3×	57	1.4k
Florence Niel France	17	879 1.1×	82 0.2×	123 0.4×	144 0.5×	125 0.4×	24	1.3k
Sirpa Ala‐Mello Finland	17	498 0.6×	140 0.3×	187 0.6×	88 0.3×	142 0.5×	29	1.2k
Alex Magee United Kingdom	12	507 0.6×	149 0.3×	120 0.4×	93 0.3×	71 0.2×	20	913
L. A. Sandkuyl Netherlands	18	550 0.7×	182 0.4×	111 0.4×	43 0.1×	101 0.3×	29	1.1k
Bradley W. Popovich United States	19	802 1.0×	128 0.3×	35 0.1×	301 1.0×	218 0.7×	28	1.7k
Thomas M. Coyne United States	14	363 0.5×	433 0.9×	206 0.7×	57 0.2×	153 0.5×	23	982
Charles W. McCluggage United States	13	175 0.2×	215 0.4×	96 0.3×	125 0.4×	55 0.2×	15	689
Satu Kuure Finland	18	1.1k 1.4×	74 0.1×	131 0.4×	341 1.1×	70 0.2×	38	1.4k

Countries citing papers authored by Bernice A. Allitto

Since Specialization

Citations

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

Fields of papers citing papers by Bernice A. Allitto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bernice A. Allitto

This figure shows the co-authorship network connecting the top 25 collaborators of Bernice A. Allitto. A scholar is included among the top collaborators of Bernice A. Allitto 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 Bernice A. Allitto. Bernice A. Allitto 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

Sugarman, Elaine A., Narasimhan Nagan, Hui Zhu, et al.. (2011). Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72 400 specimens. European Journal of Human Genetics. 20(1). 27–32. 457 indexed citations breakdown →

Rohlfs, Elizabeth M., Zhaoqing Zhou, Ruth A. Heim, et al.. (2011). Cystic Fibrosis Carrier Testing in an Ethnically Diverse US Population. Clinical Chemistry. 57(6). 841–848. 55 indexed citations

Sugarman, Elaine A., Elizabeth M. Rohlfs, Lawrence M. Silverman, & Bernice A. Allitto. (2004). CFTR mutation distribution among U.S. Hispanic and African American individuals: Evaluation in cystic fibrosis patient and carrier screening populations. Genetics in Medicine. 6(5). 392–399. 57 indexed citations

Allitto, Bernice A. & Elaine A. Sugarman. (2003). Commentary on “The 1604A (R496H) mutation in Gaucher disease: genotype/phenotype correlation,” by Brautbar et al.. Blood Cells Molecules and Diseases. 31(2). 190–191. 1 indexed citations

Rohlfs, Elizabeth M., Zhaoqing Zhou, Elaine A. Sugarman, et al.. (2002). The I148T CFTR allele occurs on multiple haplotypes: A complex allele is associated with cystic fibrosis. Genetics in Medicine. 4(5). 319–323. 56 indexed citations

Richards, Carolyn Sue, Linda Bradley, Jean Amos, et al.. (2002). Standards and Guidelines for CFTR Mutation Testing. Genetics in Medicine. 4(5). 379–391. 90 indexed citations

Heim, Ruth A., Elaine A. Sugarman, & Bernice A. Allitto. (2001). Improved detection of cystic fibrosis mutations in the heterogeneous U.S. population using an expanded, pan-ethnic mutation panel. Genetics in Medicine. 3(3). 168–176. 80 indexed citations

Finucane, Brenda, et al.. (1999). Fragile X mutation screening among unselected pregnant women seen for genetic counseling: Findings of a pilot study. Genetics in Medicine. 1(2). 54–54. 1 indexed citations

Allitto, Bernice A., L. Michaud, Sansnee Chatkupt, et al.. (1994). Paternal isodisomy for chromosome 5 in a child with spinal muscular atrophy.. PubMed. 54(3). 482–8. 36 indexed citations

10.

Allitto, Bernice A., Andrea I. McClatchey, Glenn Barnes, et al.. (1992). Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington's disease region of chromosome 4. Molecular and Cellular Probes. 6(6). 513–520. 4 indexed citations

11.

MacDonald, Marcy E., Andrea Novelletto, Carol Sze Ki Lin, et al.. (1992). The Huntington's disease candidate region exhibits many different haplotypes. Nature Genetics. 1(2). 99–103. 118 indexed citations

12.

Allitto, Bernice A., Glenn T. Horn, Michael R. Altherr, et al.. (1991). Detection by PCR of the VNTR polymorphism at D4S95. Nucleic Acids Research. 19(14). 4015–4015. 13 indexed citations

13.

Allitto, Bernice A., Marcy E. MacDonald, Maja Bućan, et al.. (1991). Increased recombination adjacent to the Huntington disease-linked D4S10 marker. Genomics. 9(1). 104–112. 42 indexed citations

14.

Whaley, William L., Gillian P. Bates, Andrea Novelletto, et al.. (1991). Mapping of cosmid clones in Huntington's disease region of chromosome 4. Somatic Cell and Molecular Genetics. 17(1). 83–91. 40 indexed citations

15.

Bates, Gillian P., Marcy E. MacDonald, Sarah Baxendale, et al.. (1990). A yeast artificial chromosome telomere clone spanning a possible location of the Huntington disease gene.. PubMed. 46(4). 762–75. 56 indexed citations

16.

MacDonald, Marcy E., Michael Zimmer, Jonathan L. Haines, et al.. (1989). Clustering of multiallele DNA markers near the Huntington's disease gene.. Journal of Clinical Investigation. 84(3). 1013–1016. 48 indexed citations

17.

MacDonald, Marcy E., Jonathan L. Haines, Michael Zimmer, et al.. (1989). Recombination events suggest potential sites for the Huntington's disease gene. Neuron. 3(2). 183–190. 79 indexed citations

18.

Allitto, Bernice A. & Kathleen M. Karrer. (1986). A family of DNA sequences is reproducibly rearranged in the somatic nucleus ofTetrahymena. Nucleic Acids Research. 14(20). 8007–8025. 11 indexed citations

19.

Kutteh, William H., Stanley A. Gall, George J. Doellgast, Bernice A. Allitto, & Jeffrey R. Dawson. (1984). Quantitation of immunoglobulins in the effusions of human ovarian epithelial neoplasms. American Journal of Obstetrics and Gynecology. 150(1). 65–69. 5 indexed citations

20.

Karrer, Kathleen M., et al.. (1984). Micronucleus-specific DNA sequences in an amicronucleate mutant of Tetrahymena. Developmental Biology. 105(1). 121–129. 25 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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