Michael M. Kaback

5.7k citations

111 papers · 4.1k indexed · 1 hit paper · h-index 35

Impact in

Genetics top 1%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
Physiology top 2%
- Lysosomal Storage Disorders Research

Papers in

Physiology 48
- Lysosomal Storage Disorders Research 46
Pediatrics, Perinatology and Child Health 20
- Prenatal Screening and Diagnostics 15

Co-authors: Jeffery P. Struewing Lawrence C. Brody Dvorah Abeliovich Francis S. Collins Tamar Peretz Elizabeth F. Neufeld R. Rodney Howell Barry H. Paw
Journals: Pediatric Research (8 papers)Pediatric Clinics of North America (4 papers)New England Journal of Medicine (4 papers)Genetics in Medicine (3 papers)American Journal of Obstetrics and Gynecology (3 papers)
Partner nations: United States Canada United Kingdom

In The Last Decade

Michael M. Kaback

109 papers receiving 3.8k citations

Hit Papers

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The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals 1995 · 512 citations

Peers

Countries citing papers authored by Michael M. Kaback

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

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

All Works

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20 of 20 papers shown

#	Work
1	Michael Kaback: people and places Genetics in Medicine ·Michael M. Kaback	2014	3
2	Genetic screening in the Persian Jewish community: A pilot study Genetics in Medicine ·Michael M. Kaback, UM Chaskar, Robin Thomas, Elva Ramírez, Mitchel Pariani, Kiichiro Ohta, David L. Rimoin	2010	18
3	Maimon M. Cohen: January 24, 1935, to January 25, 2007 The American Journal of Human Genetics ·Kurt Hirschhorn, Michael M. Kaback, David L. Rimoin	2007	1
4	Eight novel mutations in the HEXA gene Genetics in Medicine ·Matthew J. McGinniss, David Brown, Zeinab Abdelaziz El-Sherif, Molly Marten, Martina. Meidl, Michael M. Kaback	2002	6
5	27. Future perspectives for Tay-Sachs disease Advances in genetics ·Robert J. Desnick, Michael M. Kaback	2001	10
6	20. Screening and prevention in Tay-Sachs disease: Origins, update, and impact Advances in genetics ·Michael M. Kaback	2001	54
7	The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1% Nature Genetics ·Anis Nasuha, Jeffery P. Struewing, A Rafi, Susan L. Neuhausen, Lawrence C. Brody, Michael M. Kaback, Bruce R. Haas, Larry Norton, Patrick I. Borgen, Suresh C. Jhanwar, David E. Goldgar, Harry Ostrer, Kenneth Offit	1996	298
8	The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals Nature Genetics ·Jeffery P. Struewing, Dvorah Abeliovich, Tamar Peretz, B. Schlitt, Michael M. Kaback, Francis S. Collins, Lawrence C. Brody Hit paper breakdown →	1995	512
9	The Ashkenazi Jewish Fanconi anemia mutation: Incidence among patients and carrier frequency in the at-risk population Human Mutation ·Michael Whitney, Petra Jakobs, Michael M. Kaback, Robb E. Moses, Markus Grompe	1994	36
10	A Pst^+ Polymorphism in the HEXA Gene with an Unusual Geographie Distribution European Journal of Human Genetics ·Feige Kaplan, Sanjay Kapoor, K. W. Kwochka, Mariana Fernandes, László Gobi, Natal'ya Rubcova, C R Scriver, Martina. Meidl, Michael M. Kaback, Yaohua Bai, Monica Oguta, Batsheva Bonné‐Tamir, M. Tolksdorf, Martin Bobrow, Peter Hechtman	1993	5
11	A mutation common in non-jewish Tay-Sachs disease: Frequency and RNA studies Human Mutation ·Beverly R. Akerman, Julian Zielenski, Barbara L. Triggs‐Raine, E M Prence, Marvin R. Natowicz, Martina. Meidl, Michael M. Kaback, Emilie H. Mules, Gilles Thomas, Joe T.R. Clarke, R A Gravel	1992	34
12	Clinico‐pathological report: A 7‐year old white‐male boy with progressive neurological deterioration American Journal of Medical Genetics ·Lewis A. Barness, Keith Henry, Pamela J. Kling, Renata Laxová, Michael M. Kaback, Enid Gilbert‐Barness	1991	5
13	The American Society of Human Genetics statement on cystic fibrosis screening. PubMed ·C. T. Caskey, Michael M. Kaback, A L Beaudet	1990	70
14	Sandhoff disease heterozygote detection: a component of population screening for Tay-Sachs disease carriers. II. Sandhoff disease gene frequencies in American Jewish and non-Jewish populations. PubMed ·李亮伟, Christopher D. Roy, Victoria Munro, Michael M. Kaback	1987	11
15	The Tay-Sachs disease gene in North American Jewish populations: geographic variations and origin. PubMed ·Gloria M. Petersen, Jerome I. Rotter, 李亮伟, L. Leigh Field, Bhoya Urvesh, Victoria Munro, Christopher D. Roy, М. И. Панасюк, J. A. Lowden, Michael M. Kaback	1983	67
16	Estimation of the frequency of hexosaminidase a variant alleles in the American Jewish population. PubMed ·David A. Greenberg, Michael M. Kaback	1982	24
17	Genetic issues in pediatric and obstetric practice Andalas University Repository (Andalas University) ·Michael M. Kaback	1981	3
18	Regional mapping of ADA and ITP on human chromosome 20: cytogenetic and somatic cell studies in an X/20 translocation Cytogenetic and Genome Research ·T. Mohandas, R S Sparkes, Merry Passage, M.C. Sparkes, Judith H. Miles, Michael M. Kaback	1980	32
19	Allelic mutations in the mucopolysaccharidoses. PubMed ·Jaakko Leisti, D L Rimoin, Michael M. Kaback, Larry J. Shapiro, Reuben Matalon	1976	4
20	Intrauterine fetal visualization : a multidisciplinary approach Michael M. Kaback, Carlo Valenti	1976	3

About Michael M. Kaback

Michael M. Kaback is a scholar working on Physiology, Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology 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 (46 papers), Carbohydrate Chemistry and Synthesis (16 papers), Prenatal Screening and Diagnostics (15 papers), Trypanosoma species research and implications (14 papers), Glycosylation and Glycoproteins Research (11 papers), BRCA gene mutations in cancer (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Child Nutrition and Feeding Issues (7 papers). The work is most often cited by research in Genetics (1.6k citations), Physiology (1.1k citations), Pediatrics, Perinatology and Child Health (626 citations), Genetics (278 citations) and Developmental Neuroscience (105 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, Dvorah Abeliovich, Francis S. Collins, Tamar Peretz, 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, Genetics in Medicine and American Journal of Obstetrics and Gynecology.

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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