Sara Kaffe

1.2k citations

30 papers · 768 indexed · h-index 16

Impact in

Pediatrics, Perinatology and Child Health top 5%
- Prenatal Screening and Diagnostics
Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Connective tissue disorders research
- Genetics and Neurodevelopmental Disorders

Papers in

Pediatrics, Perinatology and Child Health 18
- Prenatal Screening and Diagnostics 15
Genetics 18
- Genomic variations and chromosomal abnormalities 12
- Genetic Syndromes and Imprinting 4

Co-authors: Kurt Hirschhorn Lillian Y. F. Hsu Theresa E. Perlis Philip D. Cotter Darwin J. Prockop Leslie D. McCurdy Judith P. Willner Lynn Godmilow
Journals: Prenatal Diagnosis (6 papers)Journal of Medical Genetics (4 papers)Clinical Genetics (3 papers)Genetics in Medicine (1 paper)Human Genetics (1 paper)
Partner nations: United States Israel South Korea

In The Last Decade

Sara Kaffe

30 papers receiving 697 citations

Peers

Countries citing papers authored by Sara Kaffe

Since Specialization

Citations

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

Fields of papers citing papers by Sara Kaffe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Sara Kaffe, 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 Sara Kaffe Line = papers co-authored together Sara Kaffe links everyone, so they are left out of the graph.

All Works

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

20 of 20 papers shown

#	Work
1	Skeletal defects in paternal uniparental disomy for chromosome 14 are re-capitulated in the mouse model (paternal uniparental disomy 12) Human Genetics ·V. Reid Sutton, William H. McAlister, Terry Bertin, Sara Kaffe, Haltenhoff Melani, Shoji Yano, Lisa G. Shaffer, Brendan Lee, Charles J. Epstein, Angela J. Villar	2003	38
2	Loss of subtelomeric sequence associated with a terminal inversion duplication of the short arm of chromosome 4 American Journal of Medical Genetics ·Philip D. Cotter, Sara Kaffe, Lei Li, O. Mbaye, Kurt Hirschhorn	2001	37
3	Clinical applications of comparative genomic hybridization Genetics in Medicine ·Brynn Levy, Teresa Dunn, Sara Kaffe, Nataline B. Kardon, Kurt Hirschhorn	1998	51
4	Paternal uniparental disomy for chromosome 14: A case report and review American Journal of Medical Genetics ·Philip D. Cotter, Sara Kaffe, Leslie D. McCurdy, Han Pei-h, Judith P. Willner, Kurt Hirschhorn	1997	83
5	Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies Prenatal Diagnosis ·Lillian Y. F. Hsu, Sara Kaffe, Edmund C. Jenkins, Jascha Marnette, Peter Benn, Karen David, Kurt Hirschhorn, Ernest Lieber, Alan Shanske, Lawrence R. Shapiro, P.J.W. Rowell, Dorothy Warburton	1992	105
6	Maternal serum α‐fetoprotein screening and fetal chromosome anomalies: Is lowering maternal age for amniocentesis preferable? American Journal of Medical Genetics ·Sara Kaffe, Lillian Y. F. Hsu	1992	4
7	Prenatal diagnosis of Roberts syndrome Prenatal Diagnosis ·Kurt Hirschhorn, Sara Kaffe	1992	1
8	A revisit of trisomy 20 mosaicism in prenatal diagnosis—an overview of 103 cases Prenatal Diagnosis ·Lillian Y. F. Hsu, Sara Kaffe, Theresa E. Perlis	1991	68
9	A rare case of 68,XX triploidy diagnosed by amniocentesis Prenatal Diagnosis ·Sara Kaffe, 覺樋口, Livia Wan, Norman C. Charles, Valerie Jansen, M. Alba Greco, Lillian Y. F. Hsu	1989	5
10	Amniotic fluid alpha‐fetoprotein levels and prenatal diagnosis of autosomal trisomies Prenatal Diagnosis ·Sara Kaffe, Theresa E. Perlis, Lillian Y. F. Hsu	1988	6
11	Unilateral Microscopic Gonadoblastoma in a Prepubertal Turner Mosaic with Y Chromosome Material Identified by Restriction Fragment Analysis American Journal of Clinical Pathology ·Alex Ng Hou Hong, Sara Kaffe, Fiona J. Gilbert, Stephen E. Dolgin, Ute Tintemann	1988	11
12	Trisomy 20 mosaicism in prenatal diagnosis–a review and update Prenatal Diagnosis ·Yuxiang DONG, Sara Kaffe, Theresa E. Perlis	1987	45
13	A heterozygous defect for structurally altered pro-alpha 2 chain of type I procollagen in a mild variant of osteogenesis imperfecta. The altered structure decreases the thermal stability of procollagen and makes it resistant to procollagen N-proteinase. Journal of Biological Chemistry ·Li Hua Tan, Sara Kaffe, Darwin J. Prockop	1984	58
14	Identification of Chromosomal Disorders - An Update Journal of Pediatric Ophthalmology & Strabismus ·Sara Kaffe	1983	1
15	Autosomal Dominant Inheritance of Retinoschisis American Journal of Ophthalmology ·Y Yassur, I. Nissenkorn, I Ben-Sira, Sara Kaffe, Richard M. Goodman	1982	30
16	Prenatal diagnosis of bilateral renal agenesis. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·Sara Kaffe, Lynn Godmilow, Xi-Yuan Yan, Kurt Hirschhorn	1977	25
17	Supernumerary small ring chromosome. Journal of Medical Genetics ·Sara Kaffe, Nora Yosef, L Y Hsu, Charles B. Brill, Kurt Hirschhorn	1977	3
18	Partial deletion of long arm of chromosome 11: del (11) (q23) Clinical Genetics ·Sara Kaffe, Lillian Y. F. Hsu, A. Kazykbekova, Joseph B. Philips, Kurt Hirschhorn	1977	28
19	Alkaline phosphatase activity in cultured skin fibroblasts from fibrodysplasia ossificans progressiva. Journal of Medical Genetics ·Nicholas G. Beratis, Sara Kaffe, Alan M. Aron, K Demirkol	1976	6
20	Variable cell-mediated immune defects in a family with `Candida endocrinopathy syndrome' Clinical & Experimental Immunology ·Sara Kaffe, Augusto Torrico Rojas, Linda Cahill, I P Cohen, Izabela Pereira Fraga, Kurt Hirschhorn, Platon S. Papageorgiou	1975	19

About Sara Kaffe

Sara Kaffe is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Clinical Biochemistry, Oral Surgery and Cancer Research, having authored 30 papers that have together received 768 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (15 papers), Genomic variations and chromosomal abnormalities (12 papers), Congenital Anomalies and Fetal Surgery (5 papers), Genetic Syndromes and Imprinting (4 papers), Chromosomal and Genetic Variations (4 papers), DNA Repair Mechanisms (2 papers), Immunodeficiency and Autoimmune Disorders (2 papers) and Renal and related cancers (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (399 citations), Genetics (546 citations), Developmental Biology (20 citations), Genetics (44 citations) and Urology (22 citations). Sara Kaffe has collaborated with scholars based in United States, Israel and South Korea. Frequent co-authors include Kurt Hirschhorn, Lillian Y. F. Hsu, Theresa E. Perlis, Philip D. Cotter, Darwin J. Prockop, Leslie D. McCurdy, Judith P. Willner, Lynn Godmilow, Karen David and Nataline B. Kardon. Their work appears in journals such as Prenatal Diagnosis, Journal of Medical Genetics, Clinical Genetics, Genetics in Medicine and Human Genetics.

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