LaDonna Immken

2.2k citations

21 papers · 689 indexed · h-index 13

Molecular Biology
Genetics top 10%
Genetics top 10%
Pediatrics, Perinatology and Child Health top 10%
Surgery

Co-authors: Songya Pang Sau Wai Cheung Gayle Patel Bob Marshall Marilyn S. Pollack Paweł Stankiewicz L R Carlock Ankita Patel
Topics: Genomic variations and chromosomal abnormalities (8 papers)Genetics and Neurodevelopmental Disorders (6 papers)Congenital heart defects research (5 papers)
Cited by: Genetics Clinical Biochemistry
Journals: New England Journal of Medicine Nature Genetics The Journal of Clinical Endocrinology & Metabolism
Partner nations: United States Germany Poland

In The Last Decade

LaDonna Immken

21 papers receiving 669 citations

Peers

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

#	Work	Indexed citations
1	Heterozygous variants in PRPF8 are associated with neurodevelopmental disorders 2021 ·Molecular Genetics and Metabolism ·(unknown),David A. Sweetser,Nina B. Gold,Samantha A. Schrier Vergano,Trevor L. Hoffman,Sara Cherny,(unknown),Laura Schultz‐Rogers,Wendy K. Chung,(unknown),LaDonna Immken,Susan Holder,(unknown),François Lecoquierre,Anne‐Marie Guerrot,Lance H. Rodan,Dean Sarco	1
2	Diagnostic exome sequencing identifies GLI 2 haploinsufficiency and chromosome 20 uniparental disomy in a patient with developmental anomalies 2018 ·Clinical Case Reports ·Samin A. Sajan,Zöe Powis,Katherine L. Helbig,(unknown),LaDonna Immken,Sha Tang,Wendy Alcaraz	3
3	Microdeletions excluding YWHAE and PAFAH1B1 cause a unique leukoencephalopathy: further delineation of the 17p13.3 microdeletion spectrum 2018 ·Genetics in Medicine ·Lisa Emrick,Jill A. Rosenfeld,Seema R. Lalani,Mahim Jain,Nilesh Desai,Austin Larson,(unknown),Adeline Vanderver,Ryan J. Taft,(unknown),Denise Perry,(unknown),LaDonna Immken,Lindsay C. Burrage,Carlos A. Bacino,John W. Belmont,Brendan Lee	11
4	MED resulting from recessively inherited mutations in the gene encoding calcium‐activated nucleotidase CANT1 2017 ·American Journal of Medical Genetics Part A ·(unknown),Bing Li,Deborah Krakow,Lisette Nevarez,(unknown),(unknown),Deborah A. Nickerson,Michael J. Bamshad,LaDonna Immken,Ralph S. Lachman,Daniel H. Cohn	21
5	Whole exome sequencing reveals de novo pathogenic variants in KAT6A as a cause of a neurodevelopmental disorder 2016 ·American Journal of Medical Genetics Part A ·Francisca Millan,Megan T. Cho,Kyle Retterer,Kristin G. Monaghan,Renkui Bai,Patrik Vitazka,David B. Everman,Brooke Smith,Brad Angle,Victoria H. J. Roberts,LaDonna Immken,(unknown),Marc DiFazio,Elliott H. Sherr,Eden Haverfield,Bethany Friedman,Aida Telegrafi,Jane Juusola,Wendy K. Chung,Sherri J. Bale	42
6	Intragenic deletions of the IGF1 receptor gene in five individuals with psychiatric phenotypes and developmental delay 2013 ·European Journal of Human Genetics ·Jens Witsch,Przemysław Szafrański,Chun‐An Chen,LaDonna Immken,Gayle Patel,Patricia Hixson,Sau Wai Cheung,Paweł Stankiewicz,Christian P. Schaaf	10
7	Clinical Comparison of Overlapping Deletions of 19p13.3 2013 ·American Journal of Medical Genetics Part A ·Hiba Risheg,Romela Pasion,(unknown),Virginia K. Proud,LaDonna Immken,Stuart Schwartz,(unknown),Peter Papenhausen,Tiong Yang Tan,Joris Andrieux,Ghislaine Plessis,David J. Amor,Elisabeth A. Keitges	9
8	Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders 2012 ·Molecular Cytogenetics ·Patrícia B. S. Celestino-Soper,Cindy Skinner,Richard J. Schroer,Patricia A. Eng,(unknown),(unknown),Deborah Terespolsky,(unknown),Gayle Patel,LaDonna Immken,Alecia Willis,Joanna Wiszniewska,Reuben Matalon,Jill A. Rosenfeld,Roger E. Stevenson,Sung-Hae L. Kang,Sau Wai Cheung,Arthur L. Beaudet,Paweł Stankiewicz	41
9	Deletions of Xp provide evidence for the role of holocytochrome C‐type synthase (HCCS) in congenital diaphragmatic hernia 2010 ·American Journal of Medical Genetics Part A ·(unknown),David Pearson,Gayle Patel,Barbara R. Pober,LaDonna Immken,Sau Wai Cheung,Daryl A. Scott	14
10	A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes 2009 ·Nature Genetics ·Marwan Shinawi,Christian P. Schaaf,Samarth Bhatt,Zhilian Xia,Ankita Patel,Sau Wai Cheung,Brendan C. Lanpher,Sandra Nagl,(unknown),Claudia Nevinny-Stickel,LaDonna Immken,Gayle Patel,Jennifer R. German,Arthur L. Beaudet,Paweł Stankiewicz	141
11	Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping 2009 ·Human Genetics ·Ayman W. El‐Hattab,Teresa A. Smolarek,(unknown),Elizabeth K. Schorry,LaDonna Immken,Gayle Patel,Mary‐Alice Abbott,Brendan C. Lanpher,Zhishuo Ou,Sung‐Hae Kang,Ankita Patel,Fernando Scaglia,James R. Lupski,Sau Wai Cheung,Paweł Stankiewicz	56
12	Maternal side effects of prenatal dexamethasone therapy for fetal congenital adrenal hyperplasia. 1992 ·The Journal of Clinical Endocrinology & Metabolism ·Songya Pang,(unknown),Lisa C. Freeman,Larry Dolan,LaDonna Immken,O. Thomas Mueller,Dwight D. Stiff,Dorothy I. Shulman	54
13	Prenatal Treatment of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency 1990 ·New England Journal of Medicine ·Songya Pang,Marilyn S. Pollack,Bob Marshall,LaDonna Immken	69
14	Coexistence of myelodysplastic syndrome and untreated chronic lymphocytic leukemia with development of acute myeloid leukemia immediately after treatment of chronic lymphocytic leukemia 1989 ·American Journal of Hematology ·Arthur Bracey,Anne‐Marie Maddox,LaDonna Immken,Su Ming Hsu,Michael Marks	19
15	The Nager syndrome 1987 ·American Journal of Medical Genetics ·Jacqueline T. Hecht,LaDonna Immken,(unknown),Srini Malini,Charles I. Scott,John M. Opitz,James F. Reynolds	33
16	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 1984 ·American Journal of Medical Genetics ·H. Chen,LaDonna Immken,Ralph Lachman,Samuel Yang,David L. Rimoin,(unknown),(unknown),FHC Stewart,F. A. Beemer,John M. Opitz,Enid F. Gilbert,Leonard O. Langer,Lawrence R. Shapiro,Peter A. Duncan	60
17	The steroid sulfatase locus on structurally abnormal inactive X chromosomes is expressed. 1984 ·PubMed ·LaDonna Immken,T. Mohandas,R S Sparkes,Larry J. Shapiro	7
18	The Pena‐Shokeir syndrome: Report of five cases and further delineation of the syndrome 1983 ·American Journal of Medical Genetics ·H. Chen,Bruce Blumberg,LaDonna Immken,Ralph Lachman,(unknown),(unknown),(unknown),F. A. Beemer	46
19	Significant of meconium stained fluid in midtrimester amniocentesis. 1982 ·PubMed ·LaDonna Immken,Lee M,Robert Stewart,(unknown)	1
20	SITE OF ACTION OF 3',5'-CYCLIC ADENOSINE MONOPHOSPHATE IN PRODUCTION OF TRYPTOPHANASE IN ESCHERICHIA COLI 1972 ·Genetics ·LaDonna Immken,David Apirion	1

About LaDonna Immken

LaDonna Immken is a scholar working on Genetics, Genetics and Molecular Biology, having authored 21 papers that have together received 689 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Congenital heart defects research (5 papers). The work is most often cited by research in Genetics (339 citations), Genetics (115 citations) and Clinical Biochemistry (48 citations). LaDonna Immken has collaborated with scholars based in United States, Germany and Poland. Frequent 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. Their work appears in journals such as New England Journal of Medicine, Nature Genetics and The Journal of Clinical Endocrinology & Metabolism.

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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