Ernest Lieber

844 total citations
24 papers, 581 citations indexed

About

Ernest Lieber is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ernest Lieber has authored 24 papers receiving a total of 581 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 10 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ernest Lieber's work include Prenatal Screening and Diagnostics (6 papers), Genetic Syndromes and Imprinting (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Ernest Lieber is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Genetic Syndromes and Imprinting (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Ernest Lieber collaborates with scholars based in United States, Qatar and South Korea. Ernest Lieber's co-authors include Audrey Heimler, John M. Opitz, Lillian Y. F. Hsu, Kurt Hirschhorn, James F. Reynolds, Lawrence R. Shapiro, Stephen S. Wachtel, Harvey Dosik, Ira M. Rosenthal and Paul Saenger and has published in prestigious journals such as New England Journal of Medicine, The Lancet and The American Journal of Human Genetics.

In The Last Decade

Ernest Lieber

24 papers receiving 522 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ernest Lieber United States 10 312 230 178 119 79 24 581
de Grouchy J France 14 467 1.5× 375 1.6× 191 1.1× 78 0.7× 182 2.3× 103 854
B. Rafael Elejalde United States 15 467 1.5× 357 1.6× 230 1.3× 122 1.0× 33 0.4× 39 833
Frederick W. Luthardt United States 17 318 1.0× 387 1.7× 191 1.1× 89 0.7× 99 1.3× 28 890
J G Lesko United States 12 274 0.9× 383 1.7× 308 1.7× 93 0.8× 42 0.5× 15 805
P. Petit Belgium 16 465 1.5× 261 1.1× 145 0.8× 85 0.7× 230 2.9× 72 765
F. J. Dill Canada 16 579 1.9× 242 1.1× 486 2.7× 112 0.9× 105 1.3× 24 897
H.‐D. Rott Germany 13 342 1.1× 212 0.9× 127 0.7× 63 0.5× 118 1.5× 40 639
Herman E. Wyandt United States 15 359 1.2× 205 0.9× 169 0.9× 27 0.2× 108 1.4× 40 517
Judith Dagan Israel 12 223 0.7× 231 1.0× 96 0.5× 53 0.4× 88 1.1× 27 457
Barbara K. Hecht United States 14 323 1.0× 334 1.5× 77 0.4× 95 0.8× 67 0.8× 23 693

Countries citing papers authored by Ernest Lieber

Since Specialization
Citations

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

Fields of papers citing papers by Ernest Lieber

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ernest Lieber

This figure shows the co-authorship network connecting the top 25 collaborators of Ernest Lieber. A scholar is included among the top collaborators of Ernest Lieber 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 Ernest Lieber. Ernest Lieber 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.
Lieber, Ernest, et al.. (2010). Protein Tyrosine Phosphatase PTPN14 Is a Regulator of Lymphatic Function and Choanal Development in Humans. The American Journal of Human Genetics. 87(3). 436–444. 64 indexed citations
2.
Khatwa, Umakanth, B.K. Rajegowda, Henrietta Kotlus Rosenberg, & Ernest Lieber. (2005). McKusick-Kaufman Syndrome (MK catalogue #236700) Presenting Prenatally as Fetal Abdominal Mass. Journal of Perinatology. 25(2). 146–149. 2 indexed citations
3.
Lieber, Ernest, et al.. (2003). Hydrocephalus in a hydropic fetus with Turner syndrome: a rare association. The Journal of Maternal-Fetal & Neonatal Medicine. 14(2). 136–138. 2 indexed citations
4.
Levy, Joseph, Wendy Chung, Maria C. Garzón, et al.. (2002). Congenital myopathy, recurrent secretory diarrhea, bullous eruption of skin, microcephaly, and deafness: A new genetic syndrome?. American Journal of Medical Genetics Part A. 116A(1). 20–25. 2 indexed citations
5.
George, Erik, et al.. (2000). Ellis van Creveld syndrome (chondroectodermal dysplasia, MIM 22550) in three siblings from a non-consanguineous mating. Journal of Perinatal Medicine. 28(6). 425–7. 3 indexed citations
6.
Hsu, Lillian Y. F., Sara Kaffe, Edmund C. Jenkins, et al.. (1992). Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies. Prenatal Diagnosis. 12(7). 555–573. 105 indexed citations
7.
Schwartz, Stuart, Martin Harris, Ann‐Leslie Zaslav, et al.. (1991). De novo 13q partial duplication identified by cytogenetic, biochemical and molecular approaches. Clinical Genetics. 40(6). 417–422. 2 indexed citations
8.
Lieber, Ernest, et al.. (1986). Diagnostic applications of H‐Y serology: H‐Y negative phenotype in cells from 45, X/ 46, XY fetus with testes. Clinical Genetics. 30(5). 366–373. 4 indexed citations
9.
Heimler, Audrey, Ernest Lieber, John M. Opitz, & James F. Reynolds. (1986). Branchio‐oto‐renal syndrome: Reduced penetrance and variable expressivity in four generations of a large kindred. American Journal of Medical Genetics. 25(1). 15–27. 86 indexed citations
10.
Lieber, Ernest & Payal D. Shah. (1982). Two Robertsonian translocations in a boy with mental retardation. Journal of Medical Genetics. 19(3). 229–232. 19 indexed citations
11.
Kardon, Nataline B., Ernest Lieber, Jessica G. Davis, & Lillian Y. F. Hsu. (1979). Prenatal diagnosis of trisomy 20 mosaicism. Clinical Genetics. 15(3). 267–272. 12 indexed citations
12.
Lieber, Ernest, et al.. (1978). Hazards of amniocentesis: An unidentifiable fragment. Clinical Genetics. 14(3). 130–132. 7 indexed citations
13.
Wachtel, Stephen S., Gloria C. Koo, W. Roy Breg, et al.. (1976). Serologic Detection of a Y-Linked Gene in XX Males and XX True Hermaphrodites. New England Journal of Medicine. 295(14). 750–754. 116 indexed citations
14.
Lieber, Ernest. (1973). Brachmann-de Lange Syndrome. American journal of diseases of children. 125(5). 717–717. 18 indexed citations
15.
Lieber, Ernest, et al.. (1973). FERTILITY IN A 45X/46XX PATIENT. The Lancet. 301(7796). 199–199. 9 indexed citations
16.
Lieber, Ernest, et al.. (1972). Cytogenetic findings in a parent of a patient with Fanconi's anemia. Clinical Genetics. 3(5). 357–363. 4 indexed citations
17.
Lieber, Ernest, Steven D. Douglas, & H. Hugh Fudenberg. (1971). In vitro cytotoxicity of lymphocytes from patients with "acquired" and sex-linked agammaglobulinaemia.. PubMed. 9(5). 603–9. 8 indexed citations
18.
Hsu, Lillian Y. F., et al.. (1971). Trisomy 22: A clinical entity. The Journal of Pediatrics. 79(1). 12–19. 57 indexed citations
19.
Carr, Martin C., Ernest Lieber, & H. Hugh Fudenberg. (1970). In vitro cytolysis by human fetal lymphocytes. Cellular Immunology. 1(4). 455–458. 9 indexed citations
20.
Lieber, Ernest, et al.. (1969). Familial hypogammaglobulinemia-A.. PubMed. 27(8). 393–402. 5 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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