Michael M. Kaback
Impact in
- Genetics top 1%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Physiology top 1%
- Lysosomal Storage Disorders Research
Papers in
- Physiology 47
- Lysosomal Storage Disorders Research 45
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- Glycosylation and Glycoproteins Research 11
- Co-authors
- Jeffery P. Struewing (2 shared papers)Lawrence C. Brody (2 shared papers)Tamar Peretz (1 shared paper)Francis S. Collins (1 shared paper)Dvorah Abeliovich (1 shared paper)Elizabeth F. Neufeld (5 shared papers)R. Rodney Howell (3 shared papers)Barry H. Paw (3 shared papers)
- Journals
- Pediatric Research (8 papers)Pediatric Clinics of North America (4 papers)New England Journal of Medicine (4 papers)Prenatal Diagnosis (3 papers)Human Mutation (3 papers)
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
Michael M. Kaback
109 papers receiving 3.8k citations
Michael M. Kaback's Hit Papers
Peers
Comparison fields: 5 of 126
- Genetics 1.4k
- Physiology 1.1k
- Pediatrics, Perinatology and Child Health 533
- Developmental Neuroscience 105
- Genetics 251
Countries citing papers authored by Michael M. Kaback
This map shows the geographic impact of Michael M. Kaback'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 Michael M. Kaback with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michael M. Kaback more than expected).
Fields of papers citing papers by Michael M. Kaback
This network shows the impact of papers produced by Michael M. Kaback. 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 Michael M. Kaback. The network helps show where Michael M. Kaback may publish in the future.
Co-authors
The 25 scholars most cited alongside Michael M. Kaback, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 111 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals Hit paper breakdown → | 1995 | 511 |
| 2 | 1996 | 300 | |
| 3 | 1997 | 268 | |
| 4 | 1993 | 190 | |
| 5 | 2000 | 148 | |
| 6 | 1964 | 133 | |
| 7 | 1975 | 115 | |
| 8 | Cerebroside sulfatase activator deficiency induced metachromatic leukodystrophy. | 1981 | 114 |
| 9 | 1970 | 79 | |
| 10 | 1979 | 77 | |
| 11 | 1989 | 77 | |
| 12 | 1971 | 72 | |
| 13 | Human X-autosome translocations: differential inactivation of the X chromosome in a kindred with an X-9 translocation. | 1975 | 72 |
| 14 | The American Society of Human Genetics statement on cystic fibrosis screening. | 1990 | 69 |
| 15 | 1983 | 69 | |
| 16 | The Tay-Sachs disease gene in North American Jewish populations: geographic variations and origin. | 1983 | 68 |
| 17 | Frequency of three Hex A mutant alleles among Jewish and non-Jewish carriers identified in a Tay-Sachs screening program. | 1990 | 66 |
| 18 | A pseudodeficiency allele common in non-Jewish Tay-Sachs carriers: implications for carrier screening. | 1992 | 64 |
| 19 | 1990 | 58 | |
| 20 | 1984 | 55 |
About Michael M. Kaback
Michael M. Kaback is a scholar working on Physiology, Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health and Organic Chemistry, having authored 111 papers that have together received 4.1k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (45 papers), Prenatal Screening and Diagnostics (15 papers), Carbohydrate Chemistry and Synthesis (14 papers), Trypanosoma species research and implications (13 papers), Glycosylation and Glycoproteins Research (11 papers), BRCA gene mutations in cancer (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Congenital Anomalies and Fetal Surgery (7 papers). The work is most often cited by research in Genetics (1.4k citations), Physiology (1.1k citations), Pediatrics, Perinatology and Child Health (533 citations), Developmental Neuroscience (105 citations) and Genetics (251 citations). Michael M. Kaback has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Jeffery P. Struewing, Lawrence C. Brody, Tamar Peretz, Francis S. Collins, Dvorah Abeliovich, Elizabeth F. Neufeld, R. Rodney Howell, Barry H. Paw, Alan K. Percy and Larry J. Shapiro. Their work appears in journals such as Pediatric Research, Pediatric Clinics of North America, New England Journal of Medicine, Prenatal Diagnosis and Human Mutation.
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.