Judith D. Ranells

943 total citations
10 papers, 195 citations indexed

About

Judith D. Ranells is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Judith D. Ranells has authored 10 papers receiving a total of 195 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Judith D. Ranells's work include Genetic and rare skin diseases. (2 papers), Prenatal Screening and Diagnostics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Judith D. Ranells is often cited by papers focused on Genetic and rare skin diseases. (2 papers), Prenatal Screening and Diagnostics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Judith D. Ranells collaborates with scholars based in United States, Germany and Canada. Judith D. Ranells's co-authors include Jane D. Carver, Russell S. Kirby, Alfried Kohlschütter, Dirk J. Lefeber, Zsolt Urbán, Ron A. Wevers, Linda De Meırleır, Jolanta Sykut‐Cegielska, Jeroen van Reeuwijk and Peter Meinecke and has published in prestigious journals such as Annals of Neurology, American Journal of Ophthalmology and European Journal of Human Genetics.

In The Last Decade

Judith D. Ranells

10 papers receiving 172 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Judith D. Ranells United States	7	72	58	54	28	25	10	195
Margriet van Kogelenberg New Zealand	7	76 1.1×	87 1.5×	39 0.7×	43 1.5×	58 2.3×	9	221
Julia Werner Germany	9	40 0.6×	47 0.8×	31 0.6×	17 0.6×	9 0.4×	22	204
Laila K. Effat Egypt	11	61 0.8×	139 2.4×	18 0.3×	20 0.7×	30 1.2×	29	249
Manisha Goyal India	8	46 0.6×	48 0.8×	16 0.3×	36 1.3×	6 0.2×	43	147
Esra Deniz Papatya Çakır Türkiye	9	76 1.1×	95 1.6×	65 1.2×	11 0.4×	16 0.6×	23	235
Ewa Rutkiewicz Poland	8	108 1.5×	106 1.8×	23 0.4×	20 0.7×	10 0.4×	12	268
Rosetta Marotta Australia	9	42 0.6×	252 4.3×	51 0.9×	13 0.5×	6 0.2×	13	363
Özgür Kırbıyık Türkiye	8	83 1.2×	109 1.9×	28 0.5×	31 1.1×	3 0.1×	40	211
Benjamin Kamien Australia	9	128 1.8×	124 2.1×	20 0.4×	42 1.5×	12 0.5×	19	228
Clemens Freiberg Germany	10	124 1.7×	134 2.3×	65 1.2×	10 0.4×	55 2.2×	15	287

Countries citing papers authored by Judith D. Ranells

Since Specialization

Citations

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

Fields of papers citing papers by Judith D. Ranells

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Judith D. Ranells. 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 Judith D. Ranells. The network helps show where Judith D. Ranells may publish in the future.

Co-authorship network of co-authors of Judith D. Ranells

This figure shows the co-authorship network connecting the top 25 collaborators of Judith D. Ranells. A scholar is included among the top collaborators of Judith D. Ranells 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 Judith D. Ranells. Judith D. Ranells is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

10 of 10 papers shown

Toriello, Helga V., Miriam Erick, Jean‐Luc Alessandri, et al.. (2013). Maternal vitamin K deficient embryopathy: Association with hyperemesis gravidarum and Crohn disease. American Journal of Medical Genetics Part A. 161(3). 417–429. 21 indexed citations

Baris, Hagit, Wai‐Man Chan, Caroline Andrews, et al.. (2013). Complex cytogenetic rearrangements at the DURS1 locus in syndromic Duane retraction syndrome. Clinical Case Reports. 1(1). 30–37. 3 indexed citations

Ranells, Judith D., Jane D. Carver, & Russell S. Kirby. (2011). Infantile Hypertrophic Pyloric Stenosis: Epidemiology, Genetics, and Clinical Update. Advances in Pediatrics. 58(1). 195–206. 47 indexed citations

Kontopoulos, Eftichia V., et al.. (2008). Prenatal Diagnosis of a 4q33–4qter Deletion in a Fetus with Hydrops. Fetal Diagnosis and Therapy. 24(3). 250–253. 8 indexed citations

Morava, Éva, Dirk J. Lefeber, Zsolt Urbán, et al.. (2007). Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation. European Journal of Human Genetics. 16(1). 28–35. 47 indexed citations

Lacson, Atilano, et al.. (2002). CLINICO PATHOLOGY CONFERENCE: INFANT WITH HIGH ARCHED PALATE, BELL-SHAPED CHEST, JOINT CONTRACTURES, AND INTRAUTERINE FRACTURES. Pediatric Pathology & Molecular Medicine. 21(6). 569–584. 5 indexed citations

Sutcliffe, Maxine J., et al.. (2001). Three cell line mosaicism involving structural and numerical abnormalities of chromosome 18 in a 3.5-Year-old girl: 47,XX,+18/47,XX,+del(18)(q22)/46,XX. American Journal of Medical Genetics. 102(2). 192–199. 5 indexed citations

Flanigan, Kevin M., Thomas O. Crawford, John W. Griffin, et al.. (1998). Localization of the giant axonal neuropathy gene to chromosome 16q24. Annals of Neurology. 43(1). 143–148. 25 indexed citations

Pettenati, Mark J., Ivan Šubrt, Nagesh Rao, et al.. (1991). 45,X/47,XYY mosaicism: Clinical discrepancy between prenatally and postnatally diagnosed cases. American Journal of Medical Genetics. 39(1). 42–47. 27 indexed citations

10.

Brodsky, Michael C., Laura Davis Keppen, Charles D. Rice, & Judith D. Ranells. (1990). Ocular and Systemic Findings in the Aarskog (Facial-digital-genital) Syndrome. American Journal of Ophthalmology. 109(4). 450–456. 7 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.

Explore authors with similar magnitude of impact