Catherine A. Reiser

944 total citations
27 papers, 643 citations indexed

About

Catherine A. Reiser is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Surgery. According to data from OpenAlex, Catherine A. Reiser has authored 27 papers receiving a total of 643 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 7 papers in Pediatrics, Perinatology and Child Health and 6 papers in Surgery. Recurrent topics in Catherine A. Reiser's work include Connective tissue disorders research (6 papers), BRCA gene mutations in cancer (5 papers) and Neonatal Respiratory Health Research (5 papers). Catherine A. Reiser is often cited by papers focused on Connective tissue disorders research (6 papers), BRCA gene mutations in cancer (5 papers) and Neonatal Respiratory Health Research (5 papers). Catherine A. Reiser collaborates with scholars based in United States, Germany and Canada. Catherine A. Reiser's co-authors include Richard M. Pauli, V. Kim Horton, Alan L. Breed, Susan J. Kirkpatrick, Benjamin S. Wilfond, Philip M. Farrell, Guanghong Shen, Anita Laxova, Catherine McCarthy and Elaine H. Mischler and has published in prestigious journals such as PEDIATRICS, Human Mutation and Journal of Developmental & Behavioral Pediatrics.

In The Last Decade

Catherine A. Reiser

26 papers receiving 618 citations

Peers

Catherine A. Reiser
Janice L. B. Byrne United States
Christina Zaleski United States
Richard Pimentel United States
Lora Bean United States
Marjorie H. Royle United States
Jozien T. J. Brons Netherlands
William G. Reiner United States
Harold N. Bass United States
Anne Greb United States
Piotr Węgrzyn Poland
Janice L. B. Byrne United States
Catherine A. Reiser
Citations per year, relative to Catherine A. Reiser Catherine A. Reiser (= 1×) peers Janice L. B. Byrne

Countries citing papers authored by Catherine A. Reiser

Since Specialization
Citations

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

Fields of papers citing papers by Catherine A. Reiser

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine A. Reiser

This figure shows the co-authorship network connecting the top 25 collaborators of Catherine A. Reiser. A scholar is included among the top collaborators of Catherine A. Reiser 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 Catherine A. Reiser. Catherine A. Reiser 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.
Reiser, Catherine A., et al.. (2025). Genetic counseling training program perspectives on delivering disability‐related education. Journal of Genetic Counseling. 34(4). e70070–e70070.
2.
Reiser, Catherine A., et al.. (2024). Leadership development in genetic counseling graduate programs. Journal of Genetic Counseling. 34(1). e1906–e1906. 1 indexed citations
3.
Nusbaum, Rachel, et al.. (2020). A narrative literature review: Growing the workforce through increased fieldwork capacity in genetic counseling training programs. Journal of Genetic Counseling. 30(2). 574–587. 16 indexed citations
4.
Reiser, Catherine A.. (2019). Genetic counseling clinical supervision – A call to action. Journal of Genetic Counseling. 28(4). 727–729. 1 indexed citations
5.
Reiser, Catherine A., et al.. (2017). Working with the Hmong Population in a Genetics Setting: Genetic Counselor Perspectives. Journal of Genetic Counseling. 26(6). 1388–1400. 6 indexed citations
6.
Reiser, Catherine A., et al.. (2017). Working with the Hmong Population in a Genetics Setting: an Interpreter Perspective. Journal of Genetic Counseling. 27(3). 565–573. 12 indexed citations
7.
Jurgens, Julie A., Nara Sobreira, Peggy Modaff, et al.. (2015). NovelCOL2A1Variant (c.619G>A, p.Gly207Arg) Manifesting as a Phenotype Similar to Progressive Pseudorheumatoid Dysplasia and Spondyloepiphyseal Dysplasia, Stanescu Type. Human Mutation. 36(10). 1004–1008. 14 indexed citations
8.
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10.
Tluczek, Audrey, et al.. (2010). A Tailored Approach to Family‐Centered Genetic Counseling for Cystic Fibrosis Newborn Screening: The Wisconsin Model. Journal of Genetic Counseling. 20(2). 115–128. 27 indexed citations
11.
Mischler, Elaine H., Benjamin S. Wilfond, Norman Fost, et al.. (1998). Cystic Fibrosis Newborn Screening: Impact on Reproductive Behavior and Implications for Genetic Counseling. PEDIATRICS. 102(1). 44–52. 114 indexed citations
12.
Reiser, Catherine A., et al.. (1997). Biophysical Bases for Delayed and Aberrant Motor Development in Young Children with Achondroplasia. Journal of Developmental & Behavioral Pediatrics. 18(3). 143–150. 33 indexed citations
13.
Dasgupta, Noel R., Richard M. Pauli, V. Kim Horton, & Catherine A. Reiser. (1997). Validation of radiographic criteria for the diagnosis of Down syndrome in stillborn infants. American Journal of Medical Genetics. 72(3). 347–350. 3 indexed citations
14.
Pauli, Richard M., et al.. (1997). Prevention of fixed, angular kyphosis in achondroplasia.. Journal of Pediatric Orthopaedics. 17(6). 726–733. 55 indexed citations
15.
Pauli, Richard M., et al.. (1995). Prospective assessment of risks for cervicomedullary-junction compression in infants with achondroplasia.. PubMed. 56(3). 732–44. 101 indexed citations
16.
Pauli, Richard M., et al.. (1994). Wisconsin Stillbirth Service Program: I. Establishment and assessment of a community‐based program for etiologic investigation of intrauterine deaths. American Journal of Medical Genetics. 50(2). 116–134. 49 indexed citations
17.
Pauli, Richard M. & Catherine A. Reiser. (1994). Wisconsin Stillbirth Service Program: II. Analysis of diagnoses and diagnostic categories in the first 1,000 referrals. American Journal of Medical Genetics. 50(2). 135–153. 59 indexed citations
18.
Reiser, Catherine A., et al.. (1990). Fetal disruptions: Assessment of frequency, heterogeneity, and embryologic mechanisms in a population referred to a community‐based stillbirth assessment program. American Journal of Medical Genetics. 36(1). 56–72. 45 indexed citations
19.
Pauli, Richard M. & Catherine A. Reiser. (1984). The Wisconsin stillbirth service project: the 'Wisconsin idea' in practice. 31(1). 3 indexed citations
20.
Reiser, Catherine A., Richard M. Pauli, & Judith G. Hall. (1984). Achondroplasia: Unexpected familial recurrence. American Journal of Medical Genetics. 19(2). 245–250. 27 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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