Elizabeth Roeder

6.2k citations

37 papers · 1.9k indexed · h-index 21

Impact in

Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Cleft Lip and Palate Research
Developmental Biology top 5%

Papers in

Developmental Biology 3
- Congenital limb and hand anomalies 3
Genetics 21
- Genomic variations and chromosomal abnormalities 10
- Genetic Syndromes and Imprinting 6
- Genetics and Neurodevelopmental Disorders 6

Co-authors: Maximilian Muenke Raoul C. M. Hennekam Lucia Brown S. Stengel‐Rutkowski Dorothy Warburton Stephen Brown Chih‐Yu Yu Sau Wai Cheung
Journals: Journal of Inherited Metabolic Disease (2 papers)European Journal of Human Genetics (2 papers)Nature Genetics (1 paper)Planta Medica (1 paper)Genetics in Medicine (1 paper)
Partner nations: United States Canada Netherlands

In The Last Decade

Elizabeth Roeder

37 papers receiving 1.8k citations

Peers

Countries citing papers authored by Elizabeth Roeder

Since Specialization

Citations

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

Fields of papers citing papers by Elizabeth Roeder

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Elizabeth Roeder, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Elizabeth Roeder Line = papers co-authored together Elizabeth Roeder links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A de novo 1.58 Mb deletion, including MAP2K6 and mapping 1.28 Mb upstream to SOX9, identified in a patient with Pierre Robin sequence and osteopenia with multiple fractures American Journal of Medical Genetics Part A ·Marta Smyk, Elizabeth Roeder, Sau Wai Cheung, Przemysław Szafrański, Paweł Stankiewicz	2015	9
2	Clinical characterization of int22h1/int22h2-mediated Xq28 duplication/deletion: new cases and literature review BMC Medical Genetics ·Ayman W. El‐Hattab, Christian P. Schaaf, Ping Fang, Elizabeth Roeder, Virginia Kimonis, Joseph A. Church, Ankita Patel, Sau Wai Cheung	2015	32
3	A patient with a unique frameshift mutation in GPC3, causing Simpson–Golabi–Behmel syndrome, presenting with craniosynostosis, penoscrotal hypospadias, and a large prostatic utricle American Journal of Medical Genetics Part A ·Diana Villarreal, Humberto Villarreal, Ana Paez, Dennis S. Peppas, Jane Lynch, Elizabeth Roeder, George Powers	2013	11
4	Metastatic medulloblastoma in an adolescent with Simpson–Golabi–Behmel syndrome American Journal of Medical Genetics Part A ·Martha H. Thomas, Victoria B. Enciso, Robert F. Stratton, Shafqat Shah, Thomas Winder, Marwan K. Tayeh, Elizabeth Roeder	2012	18
5	Phenotypic manifestations of copy number variation in chromosome 16p13.11 European Journal of Human Genetics ·Sandesh C. Sreenath Nagamani, Ayelet Erez, Patricia I. Bader, Seema R. Lalani, Daryl A. Scott, Fernando Scaglia, Sharon E. Plon, Chun-Hui Tsai, Tyler Reimschisel, Elizabeth Roeder, Amy D. Malphrus, Patricia A. Eng, Patricia Hixson, Sung-Hae L. Kang, Paweł Stankiewicz, Ankita Patel, Sau Wai Cheung	2010	83
6	Tetrasomy 18p: Report of the molecular and clinical findings of 43 individuals American Journal of Medical Genetics Part A ·Courtney Sebold, Elizabeth Roeder, Marsha Zimmerman, Bridgette Soileau, Patricia Heard, Erika Carter, Martha Schatz, William A. White, Brian P. Perry, Kent A. Reinker, Louise O’Donnell, Jack L. Lancaster, John Li, Minire Hasi, Annice Hill, Lauren Pankratz, Daniel E. Hale, Jannine D. Cody	2010	50
7	Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly Diamond–Blackfan anaemia Journal of Medical Genetics ·Margaret Wat, Victoria B. Enciso, Wojciech Wiszniewski, Trevor Resnick, Patricia I. Bader, Elizabeth Roeder, Debra Freedenberg, Chester Brown, P. Stankiewicz, S.W. Cheung, Daryl A. Scott	2010	28
8	Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12 European Journal of Human Genetics ·Sandesh C. Sreenath Nagamani, Ayelet Erez, Joseph Shen, Chumei Li, Elizabeth Roeder, Sarah K. Cox, Lefkothea Karaviti, Margret Pearson, Sung‐Hae Kang, Trilochan Sahoo, Seema R. Lalani, Paweł Stankiewicz, V. Reid Sutton, Sau Wai Cheung	2009	103
9	Identification of proximal 1p36 deletions using array‐CGH: a possible new syndrome Clinical Genetics ·S‐HL Kang, A. Scheffer, Zhishuo Ou, Jessica Shu Nan Li, Fernando Scaglia, John W. Belmont, SR Lalani, Elizabeth Roeder, Victoria B. Enciso, Stephen R. Braddock, Janda L. Buchholz, Scott J. Vacha, AC Chinault, SW Cheung, CA Bacino	2007	40
10	Homozygous myotonic dystrophy: Clinical findings in two patients and review of the literature American Journal of Medical Genetics Part A ·Christine Zühlke, Elizabeth Roeder, Sabine Purmann, Dagmar Wieczorek, Cynthia J. Curry, Cheri Loustalet, Yorck Hellenbroich, Hans Helmut Richardt, Gabriele Gillessen‐Kaesbach	2007	4
11	Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including FMR1, FMR2, and IDS in a female patient with mental retardation American Journal of Medical Genetics Part A ·Frank J. Probst, Elizabeth Roeder, Victoria B. Enciso, Zhishuo Ou, M. Lance Cooper, Patricia A. Eng, Jiangzhen Li, Yanghong Gu, Robert F. Stratton, A. Craig Chinault, Chad A. Shaw, V. Reid Sutton, Sau Wai Cheung, David L. Nelson	2007	44
12	MICRO syndrome: An entity distinct from COFS syndrome American Journal of Medical Genetics Part A ·John M. Graham, Raoul C. M. Hennekam, William B. Dobyns, Elizabeth Roeder, David B. Busch	2004	35
13	Neuroprotective Effects of Hydroxysafflor Yellow A:In Vivoandin VitroStudies Planta Medica ·Haibo Zhu, Zhenhua Wang, Chengjun Ma, Jingwei Tian, Fenghua Fu, Changling Li, De‐an Guo, Elizabeth Roeder, Ke Liu	2003	96
14	Trisomy 12 mosaicism confirmed in multiple organs from a liveborn child American Journal of Medical Genetics ·C.D. DeLozier-Blanchet, Elizabeth Roeder, Riccardo Denis-Arrue, Jean‐Louis Blouin, Jackie Low, Jamie Fisher, David Scharnhorst, Cynthia J. Curry	2000	20
15	Scapuloiliac dysostosis (Kosenow syndrome, pelvis-shoulder dysplasia) spectrum: Three additional cases American Journal of Medical Genetics ·Alison M. Elliott, Elizabeth Roeder, David R. Witt, David L. Rimoin, Ralph S. Lachman	2000	8
16	Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndrome American Journal of Medical Genetics ·Angela E. Lin, Elena V. Semina, Sandra Daack‐Hirsch, Elizabeth Roeder, Cynthia J. Curry, Kenneth N. Rosenbaum, David D. Weaver, Jeffrey C. Murray	2000	12
17	Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired Nature Genetics ·Stephen Brown, Dorothy Warburton, Lucia Brown, Chih‐Yu Yu, Elizabeth Roeder, S. Stengel‐Rutkowski, Raoul C. M. Hennekam, Maximilian Muenke	1998	386
18	Cataract in early onset and classic Cockayne syndrome Ophthalmic Genetics ·R. Cruz Ferreira, Elizabeth Roeder, James Bateman	1997	6
19	Ritscher-Schinzel (3C) syndrome: Documentation of the phenotype American Journal of Medical Genetics ·Kenjiro Kosaki, Cynthia J. Curry, Elizabeth Roeder, Kenneth Lyons Jones	1997	21
20	Effect of Myotonic Dystrophy Trinucleotide Repeat Expansion on DMPK Transcription and Processing Genomics ·Ralf Krahe, Tetsuo Ashizawa, Claudia Abbruzzese, Elizabeth Roeder, Paul Carango, Manlio Giacanelli, Vicky L. Funanage, Michael J. Siciliano	1995	114

About Elizabeth Roeder

Elizabeth Roeder is a scholar working on Developmental Biology, Genetics, Urology, Pediatrics, Perinatology and Child Health and Genetics, having authored 37 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Congenital heart defects research (7 papers), Genetic Syndromes and Imprinting (6 papers), Genetics and Neurodevelopmental Disorders (6 papers), Prenatal Screening and Diagnostics (3 papers), Hedgehog Signaling Pathway Studies (3 papers), RNA modifications and cancer (3 papers) and Congenital limb and hand anomalies (3 papers). The work is most often cited by research in Genetics (972 citations), Developmental Biology (74 citations), Pediatrics, Perinatology and Child Health (346 citations), Molecular Biology (1.2k citations) and Genetics (118 citations). Elizabeth Roeder has collaborated with scholars based in United States, Canada and Netherlands. Frequent co-authors include Maximilian Muenke, Raoul C. M. Hennekam, Lucia Brown, S. Stengel‐Rutkowski, Dorothy Warburton, Stephen Brown, Chih‐Yu Yu, Sau Wai Cheung, Cynthia J. Curry and Ariel Ruiz i Altaba. Their work appears in journals such as Journal of Inherited Metabolic Disease, European Journal of Human Genetics, Nature Genetics, Planta Medica and Genetics in Medicine.

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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