Ruth A. Heim

912 total citations
21 papers, 643 citations indexed

About

Ruth A. Heim is a scholar working on Pulmonary and Respiratory Medicine, Genetics and Molecular Biology. According to data from OpenAlex, Ruth A. Heim has authored 21 papers receiving a total of 643 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Pulmonary and Respiratory Medicine, 8 papers in Genetics and 5 papers in Molecular Biology. Recurrent topics in Ruth A. Heim's work include Cystic Fibrosis Research Advances (9 papers), Neonatal Respiratory Health Research (6 papers) and Genomics and Rare Diseases (4 papers). Ruth A. Heim is often cited by papers focused on Cystic Fibrosis Research Advances (9 papers), Neonatal Respiratory Health Research (6 papers) and Genomics and Rare Diseases (4 papers). Ruth A. Heim collaborates with scholars based in United States, South Africa and Brazil. Ruth A. Heim's co-authors include Lawrence M. Silverman, Elaine A. Sugarman, Bernice A. Allitto, Michael R. Knowles, Kenneth J. Friedman, Arthur S. Aylsworth, Lauren Kam-Morgan, Michael C. Luce, Cameron G. Binnie and Matthew C. Cayouette and has published in prestigious journals such as Scientific Reports, Human Molecular Genetics and Clinical Chemistry.

In The Last Decade

Ruth A. Heim

21 papers receiving 622 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ruth A. Heim United States	13	353	155	117	111	80	21	643
Gail D. Wenger United States	11	147 0.4×	187 1.2×	60 0.5×	56 0.5×	23 0.3×	14	406
Maree V. Hammett Australia	16	119 0.3×	222 1.4×	93 0.8×	59 0.5×	40 0.5×	21	1.1k
Anna Clerico Italy	16	126 0.4×	222 1.4×	40 0.3×	202 1.8×	74 0.9×	35	590
Antonia Gaona Spain	13	354 1.0×	165 1.1×	94 0.8×	474 4.3×	81 1.0×	16	808
Amélie Pinard France	11	320 0.9×	221 1.4×	252 2.2×	46 0.4×	12 0.1×	19	650
Shantel Weinsheimer United States	15	161 0.5×	165 1.1×	70 0.6×	339 3.1×	64 0.8×	28	701
Donna C. Rich United States	7	88 0.2×	260 1.7×	176 1.5×	241 2.2×	34 0.4×	8	580
Wolfram Henn Germany	12	56 0.2×	190 1.2×	145 1.2×	89 0.8×	50 0.6×	27	540
Chisa Aoyama United States	13	166 0.5×	177 1.1×	75 0.6×	108 1.0×	11 0.1×	24	651
Cecilie F. Rustad Norway	11	80 0.2×	210 1.4×	116 1.0×	170 1.5×	72 0.9×	18	491

Countries citing papers authored by Ruth A. Heim

Since Specialization

Citations

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

Fields of papers citing papers by Ruth A. Heim

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ruth A. Heim

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

1.

Zeng, Qiandong, Natalia T. Leach, Zhaoqing Zhou, et al.. (2020). A customized scaffolds approach for the detection and phasing of complex variants by next-generation sequencing. Scientific Reports. 10(1). 15060–15060. 3 indexed citations

2.

Murphy, Elissa, et al.. (2020). A Role for Chromosomal Microarray Testing in the Workup of Male Infertility. Journal of Molecular Diagnostics. 22(9). 1189–1198. 5 indexed citations

3.

Zhu, Hui, et al.. (2019). Comparison of pan‐ethnic and ethnic‐based carrier screening panels for individuals of Ashkenazi Jewish descent. Journal of Genetic Counseling. 29(1). 56–66. 5 indexed citations

4.

Leach, Natalia T., et al.. (2018). Comparative assessment of gene-specific variant distribution in prenatal and postnatal cohorts tested for Noonan syndrome and related conditions. Genetics in Medicine. 21(2). 417–425. 15 indexed citations

5.

Hoffman, Jodi D., Nicole Schreiber‐Agus, Ruth Kornreich, et al.. (2014). The Ashkenazi Jewish carrier screening panel: evolution, status quo, and disparities. Prenatal Diagnosis. 34(12). 1161–1167. 15 indexed citations

6.

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

7.

Rohlfs, Elizabeth M., et al.. (2004). Simultaneous Detection of Multiple Point Mutations Using Allele‐Specific Oligonucleotides. Current Protocols in Human Genetics. 41(1). Unit9.4–Unit9.4. 5 indexed citations

8.

Raskin, Salmo, Francisco J.C. Reis, Nelson Augusto Rosário Filho, et al.. (2003). High Allelic Heterogeneity Between Afro-Brazilians and Euro-Brazilians Impacts Cystic Fibrosis Genetic Testing. Genetic Testing. 7(3). 213–218. 19 indexed citations

9.

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

10.

Wong, Lee‐Jun C., Jianjun Wang, Yinghua Zhang, et al.. (2001). Improved detection ofCFTR mutations in Southern California Hispanic CF patients. Human Mutation. 18(4). 296–307. 33 indexed citations

11.

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

12.

Friedman, Kenneth J., Ruth A. Heim, Michael R. Knowles, & Lawrence M. Silverman. (1997). Rapid characterization of the variable length polythymidine tract in the cystic fibrosis (CFTR) gene: Association of the 5T allele with selected CFTR mutations and its incidence in atypical sinopulmonary disease. Human Mutation. 10(2). 108–115. 67 indexed citations

13.

Friedman, Kenneth J., Ruth A. Heim, Michael R. Knowles, & Lawrence M. Silverman. (1997). Rapid characterization of the variable length polythymidine tract in the cystic fibrosis (CFTR) gene: Association of the 5T allele with selected CFTR mutations and its incidence in atypical sinopulmonary disease. Human Mutation. 10(2). 108–115. 5 indexed citations

14.

Heim, Ruth A., Lauren Kam-Morgan, Cameron G. Binnie, et al.. (1995). Distribution of 13 truncating mutations in the neurofibromatosis 1 gene. Human Molecular Genetics. 4(6). 975–981. 144 indexed citations

15.

Heim, Ruth A., Nicholas Lench, & Michael Swift. (1992). Heterozygous manifestations in four autosomal recessive human cancer-prone syndromes: ataxia telangiectasia, xeroderma pigmentosum, Fanconi anemia, and Bloom syndrome. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 284(1). 25–36. 38 indexed citations

16.

Morris, Deborah, et al.. (1992). Study of 30 DNA markers in three southern African populations.. PubMed. 5(1-2). 1–12. 3 indexed citations

17.

Heim, Ruth A., Richard A. Pierce, Susan B. Deak, et al.. (1991). Alternative Splicing of Rat Tropoelastin mRNA is Tissue-Specific and Developmentally Regulated. Matrix. 11(5). 359–366. 32 indexed citations

18.

Stolle, Catherine A., et al.. (1991). Nucleotide sequence of a cDNA encoding rat brain carbonic anhydrase II and its deduced amino acid sequence. Gene. 109(2). 265–267. 15 indexed citations

19.

Jenkins, T, Ruth A. Heim, David S. Dunn, et al.. (1990). In quest of the tyrosinase-positive oculocutaneous albinism gene. Ophthalmic Paediatrics and Genetics. 11(4). 251–254. 4 indexed citations

20.

Heim, Ruth A., et al.. (1988). The tyrosinase-positive oculocutaneous albinism locus is not linked to the ?-globin locus in man. Human Genetics. 79(1). 89–89. 8 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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