LaDonna Immken

2.2k total citations
21 papers, 689 citations indexed

About

LaDonna Immken is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, LaDonna Immken has authored 21 papers receiving a total of 689 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Genetics and 4 papers in Surgery. Recurrent topics in LaDonna Immken's work include Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Congenital heart defects research (5 papers). LaDonna Immken is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Congenital heart defects research (5 papers). LaDonna Immken collaborates with scholars based in United States, Germany and Poland. LaDonna Immken's co-authors include Songya Pang, Sau Wai Cheung, Gayle Patel, Bob Marshall, Marilyn S. Pollack, Paweł Stankiewicz, L R Carlock, Ankita Patel, John J. Wasmuth and Brendan C. Lanpher and has published in prestigious journals such as New England Journal of Medicine, Nature Genetics and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

LaDonna Immken

21 papers receiving 669 citations

Peers

LaDonna Immken

GENET

PPCH

SURGE

Robert Wallerstein United States

I. T. Thomas United States

Seher Başaran Türkiye

Memnune Yüksel‐Apak Türkiye

Mark V. Sauer United States

K Imaizumi Japan

Ali Hellani Saudi Arabia

Marion Gérard France

Joy B. Redman United States

Dilek Aktaş Türkiye

Robert Wallerstein United States

LaDonna Immken

410 ×1.1

399 ×1.2

GENET

45 ×0.4

GENET

180 ×1.6

PPCH

140 ×1.8

SURGE

Citations per year, relative to LaDonna Immken LaDonna Immken (= 1×) peers Robert Wallerstein

Countries citing papers authored by LaDonna Immken

Since Specialization

Citations

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

Fields of papers citing papers by LaDonna Immken

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by LaDonna Immken. 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 LaDonna Immken. The network helps show where LaDonna Immken may publish in the future.

Co-authorship network of co-authors of LaDonna Immken

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

Sweetser, David A., Nina B. Gold, Samantha A. Schrier Vergano, et al.. (2021). Heterozygous variants in PRPF8 are associated with neurodevelopmental disorders. Molecular Genetics and Metabolism. 132. S109–S110. 1 indexed citations

Sajan, Samin A., Zöe Powis, Katherine L. Helbig, et al.. (2018). Diagnostic exome sequencing identifies GLI 2 haploinsufficiency and chromosome 20 uniparental disomy in a patient with developmental anomalies. Clinical Case Reports. 6(7). 1208–1213. 3 indexed citations

Emrick, Lisa, Jill A. Rosenfeld, Seema R. Lalani, et al.. (2018). Microdeletions excluding YWHAE and PAFAH1B1 cause a unique leukoencephalopathy: further delineation of the 17p13.3 microdeletion spectrum. Genetics in Medicine. 21(7). 1652–1656. 11 indexed citations

Li, Bing, Deborah Krakow, Lisette Nevarez, et al.. (2017). MED resulting from recessively inherited mutations in the gene encoding calcium‐activated nucleotidase CANT1. American Journal of Medical Genetics Part A. 173(9). 2415–2421. 21 indexed citations

Millan, Francisca, Megan T. Cho, Kyle Retterer, et al.. (2016). Whole exome sequencing reveals de novo pathogenic variants in KAT6A as a cause of a neurodevelopmental disorder. American Journal of Medical Genetics Part A. 170(7). 1791–1798. 42 indexed citations

Witsch, Jens, Przemysław Szafrański, Chun‐An Chen, et al.. (2013). Intragenic deletions of the IGF1 receptor gene in five individuals with psychiatric phenotypes and developmental delay. European Journal of Human Genetics. 21(11). 1304–1307. 10 indexed citations

Risheg, Hiba, Romela Pasion, Virginia K. Proud, et al.. (2013). Clinical Comparison of Overlapping Deletions of 19p13.3. American Journal of Medical Genetics Part A. 161(5). 1110–1116. 9 indexed citations

Celestino-Soper, Patrícia B. S., Cindy Skinner, Richard J. Schroer, et al.. (2012). Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders. Molecular Cytogenetics. 5(1). 17–17. 41 indexed citations

Pearson, David, Gayle Patel, Barbara R. Pober, et al.. (2010). Deletions of Xp provide evidence for the role of holocytochrome C‐type synthase (HCCS) in congenital diaphragmatic hernia. American Journal of Medical Genetics Part A. 152A(6). 1588–1590. 14 indexed citations

10.

Shinawi, Marwan, Christian P. Schaaf, Samarth Bhatt, et al.. (2009). A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes. Nature Genetics. 41(12). 1269–1271. 141 indexed citations

11.

El‐Hattab, Ayman W., Teresa A. Smolarek, Elizabeth K. Schorry, et al.. (2009). Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping. Human Genetics. 126(4). 589–602. 56 indexed citations

12.

Pang, Songya, Lisa C. Freeman, Larry Dolan, et al.. (1992). Maternal side effects of prenatal dexamethasone therapy for fetal congenital adrenal hyperplasia.. The Journal of Clinical Endocrinology & Metabolism. 75(1). 249–253. 54 indexed citations

13.

Pang, Songya, Marilyn S. Pollack, Bob Marshall, & LaDonna Immken. (1990). Prenatal Treatment of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency. New England Journal of Medicine. 322(2). 111–115. 69 indexed citations

14.

Bracey, Arthur, Anne‐Marie Maddox, LaDonna Immken, Su Ming Hsu, & Michael Marks. (1989). Coexistence of myelodysplastic syndrome and untreated chronic lymphocytic leukemia with development of acute myeloid leukemia immediately after treatment of chronic lymphocytic leukemia. American Journal of Hematology. 30(3). 174–180. 19 indexed citations

15.

Hecht, Jacqueline T., LaDonna Immken, Srini Malini, et al.. (1987). The Nager syndrome. American Journal of Medical Genetics. 27(4). 965–969. 33 indexed citations

16.

Chen, H., LaDonna Immken, Ralph Lachman, et al.. (1984). Syndrome of multiple pterygia, camptodactyly, facial anomalies, hypoplastic lungs and heart, cystic hygroma, and skeletal anomalies: Delineation of a new entity and review of lethal forms of multiple pterygium syndrome. American Journal of Medical Genetics. 17(4). 809–826. 60 indexed citations

17.

Immken, LaDonna, T. Mohandas, R S Sparkes, & Larry J. Shapiro. (1984). The steroid sulfatase locus on structurally abnormal inactive X chromosomes is expressed.. PubMed. 36(5). 979–86. 7 indexed citations

18.

Chen, H., et al.. (1983). The Pena‐Shokeir syndrome: Report of five cases and further delineation of the syndrome. American Journal of Medical Genetics. 16(2). 213–224. 46 indexed citations

19.

Immken, LaDonna, et al.. (1982). Significant of meconium stained fluid in midtrimester amniocentesis.. PubMed. 18(3 Pt A). 187–90. 1 indexed citations

20.

Immken, LaDonna & David Apirion. (1972). SITE OF ACTION OF 3',5'-CYCLIC ADENOSINE MONOPHOSPHATE IN PRODUCTION OF TRYPTOPHANASE IN ESCHERICHIA COLI. Genetics. 70(1). 175–180. 1 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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