Mark H. Skolnick

37.7k citations

141 papers · 17.3k indexed · 5 hit papers · h-index 47

Impact in

Genetics top 0.05%
- Genetic diversity and population structure
- Genetic Mapping and Diversity in Plants and Animals
- Genetic and phenotypic traits in livestock
- BRCA gene mutations in cancer
Hematology top 0.5%
- Iron Metabolism and Disorders

Papers in

Genetics 53
- Genomic variations and chromosomal abnormalities 20
- BRCA gene mutations in cancer 17
- Genetic and rare skin diseases. 9
- Genetic Associations and Epidemiology 9
Hematology 18
- Iron Metabolism and Disorders 13

Co-authors: R. White David Botstein Ronald W. Davis Alexander Kamb Nelleke A. Gruis Sean V. Tavtigian D. Timothy Bishop Jane Weaver-Feldhaus
Journals: Genomics (8 papers)Science (6 papers)Cytogenetic and Genome Research (6 papers)New England Journal of Medicine (6 papers)Genetic Epidemiology (6 papers)
Partner nations: United States United Kingdom Italy

In The Last Decade

Mark H. Skolnick

139 papers receiving 16.2k citations

Hit Papers

5 papers align trajectories log scale

A Cell Cycle Regulator Potentially Involved in Genesis of Many Tumor Types 1994 · 2.3k citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

1994 Science
1990 Science
1988 New England Journal of Medicine
1987 Science
1980 PubMed

Peers

Countries citing papers authored by Mark H. Skolnick

Since Specialization

Citations

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

Fields of papers citing papers by Mark H. Skolnick

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mark H. Skolnick. 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 Mark H. Skolnick. The network helps show where Mark H. Skolnick may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Sequencing and assembly of highly heterozygous genome of Vitis vinifera L. cv Pinot Noir: Problems and solutions Journal of Biotechnology ·Andrey Zharkikh, Michela Troggio, Dmitry Pruss, Alessandro Cestaro, М Tykhonovska, Massimo Pindo, Victor Posligua, Silvia Vezzulli, S. K. Bhatnagar, Paolo Fontana, Roberto Viola, Alexander Gutin, Francesco Salamini, Mark H. Skolnick, Riccardo Velasco	2008	20
2	TBC1D1 is a candidate for a severe obesity gene and evidence for a gene/gene interaction in obesity predisposition Human Molecular Genetics ·Steven Stone, Victor Abkevich, Deanna L. Russell, Robyn Riley, Kirsten M. Timms, Thanh V. Tran, Foteini Xanthou, David A. Frank, Srikanth Jammulapati, Chris Neff, Diana Iliev, Richard E. Gress, Gongping He, Georges C. Frech, Ted D. Adams, Mark H. Skolnick, Jerry S. Lanchbury, Alexander Gutin, Steven C. Hunt, Donna Shattuck	2006	119
3	Genome‐wide linkage analyses of extended Utah pedigrees identifies loci that influence recurrent, early‐onset major depression and anxiety disorders American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Nicola J. Camp, Michael Lowry, Ruth Richards, Gregorio Moreno-Rueda, Guttemberg Martins da Silva, Charles H. Hensel, Victor Abkevich, Mark H. Skolnick, Donna Shattuck, Kerry Rowe, Dana C. Hughes, Lisa Cannon‐Albright	2005	80
4	Microdissection, DOP-PCR, and comparative genomic hybridization of paraffin-embedded familial prostate cancers Cancer Genetics and Cytogenetics ·Paul C.M.S. Verhagen, Xiao Lin Zhu, L. Ralph Rohr, Lisa Cannon‐Albright, Sean V. Tavtigian, Mark H. Skolnick, Arthur R. Brothman	2000	23
5	Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer Nature Genetics ·Susan L. Neuhausen, Teresa Gilewski, Larry Norton, Thao Tran, Peter J. McGuire, Jeffrey Swensen, Heather Hampel, Patrick I. Borgen, Karen Brown, Mark H. Skolnick, Donna Shattuck-Eidens, Suresh C. Jhanwar, David E. Goldgar, Kenneth Offit	1996	219
6	BRCA1 germline mutational spectrum in Italian families from Tuscany: a high frequency of novel mutations. Research Padua Archive (University of Padua) ·Maria A. Caligo, Chiara Ghimenti, Giovanna Cipollini, Sergio Ricci, I. Brunetti, Sukati Mphumuzi, Г.В. Суркова, Susan L. Neuhausen, Donna Shattuck-Eidens, Pierfranco Conté, Mark H. Skolnick, Generoso Bevilacqua	1996	41
7	Monitoring the efficacy of hybrid selection during positional cloning: the search for BRCA1 Mammalian Genome ·Thomas Hattier, Russell Bell, Daniel J. Shaffer, Steven Stone, Lynn Catterson, Sean V. Tavtigian, Mark H. Skolnick, Donna Shattuck-Eidens, Alexander Kamb	1995	3
8	Common 9p haplotype in Dutch familial atypical multiple mole-melanoma (FAMMM) syndrome families; no evidence for involvement of MTS1 The American Journal of Human Genetics ·Nelleke A. Gruis, Lodewijk A. Sandkuijl, Mark H. Skolnick	1994	2
9	Isolation of a diverged homeobox gene, M0X1, from the BRCA1 region on 17q21 by solution hybrid capture Human Molecular Genetics ·P. Andrew Futreal, Charles Cochran, Judith Rosenthal, C. Spector, Dodi Rosadi, Maurine R. Hobbs, L. Michelle Bennett, Astrid C. Haugen, 香織井城, J. Carl Barrett, Aguirre Bermúdez, R. 까비에, Alexander Kamb, Mark H. Skolnick, Roger W. Wiseman	1994	36
10	Inheritance of nevus number and size in melanoma/DNS kindreds Cytogenetic and Genome Research ·David E. Goldgar, Lisa Cannon‐Albright, Laurence J. Meyer, Michael W. Piepkorn, John J. Zone, Mark H. Skolnick	1992	4
11	Number, size, and histopathology of nevi in Utah kindreds Cytogenetic and Genome Research ·Laurence J. Meyer, David E. Goldgar, Lisa Cannon‐Albright, Michael W. Piepkorn, John J. Zone, Noemie Hurst, Mark H. Skolnick	1992	8
12	Detection of Proliferative Breast Disease Four-Quadrant, Fine-Needle Aspiration JNCI Journal of the National Cancer Institute ·John H. Ward, Catriona Marshall, Günter Schumann, Hugh H. Hogle, Lisa Cannon‐Albright, William P. McWhorter, Harmon J. Eyre, Mark H. Skolnick	1990	15
13	The dysplastic melanocytic nevus: A prevalent lesion that correlates poorly with clinical phenotype Journal of the American Academy of Dermatology ·Michael W. Piepkorn, Laurence J. Meyer, David E. Goldgar, Susanne A. Seuchter, Lisa Cannon‐Albright, Mark H. Skolnick, John J. Zone	1989	98
14	HLA-linked hemochromatosis alleles in sporadic porphyria cutanea tarda Gastroenterology ·Corwin Q. Edwards, Linda M. Griffen, David E. Goldgar, Mark H. Skolnick, James P. Kushner	1989	35
15	Characteristics of familial colon cancer in a large population data base Cancer ·Lisa Cannon‐Albright, Dang Kim Khoi, D. Timothy Bishop, Mark H. Skolnick, R. Burt	1989	34
16	Screening for Hemochromatosis in Healthy Blood Donors Annals of the New York Academy of Sciences ·Corwin Q. Edwards, Linda M. Griffen, Pongsak Limpornpipat, Mark H. Skolnick, James P. Kushner	1988	2
17	Sporadic Porphyria Cutanea Tarda in Individuals with HLA‐linked Hemochromatosis Allele(s) Annals of the New York Academy of Sciences ·Corwin Q. Edwards, Linda M. Griffen, Mark H. Skolnick, James P. Kushner	1988	3
18	Genetic analysis of NF1: Identification of close flanking markers on chromosome 17 Genomics ·Pamela R. Fain, David F. Barker, David E. Goldgar, E Wright, K. Nguyen, John C. Carey, D. E. Torres, J. Kivlin, H.F. Willard, Christopher G. Mathew, B A Ponder, Mark H. Skolnick	1987	54
19	Genetic analysis workshop II: Segregation and three‐locus linkage analysis Genetic Epidemiology ·D. Timothy Bishop, Lisa A. Cannon, Sandra J. Hasstedt, Mark H. Skolnick	1984	1
20	Utah pedigree studies: design and preliminary data for premature male CHD deaths. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·R R Williams, Mark H. Skolnick, Dorit Carmelli, Francesco Genua, Steven C. Hunt, Sandra J. Hasstedt, Gayle E. Reiber, Metty Yunita	1979	21

About Mark H. Skolnick

Mark H. Skolnick is a scholar working on Genetics, Hematology, Cancer Research, Oncology and Pathology and Forensic Medicine, having authored 141 papers that have together received 17.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (20 papers), BRCA gene mutations in cancer (17 papers), Cutaneous Melanoma Detection and Management (14 papers), Cancer Genomics and Diagnostics (13 papers), Iron Metabolism and Disorders (13 papers), Genetic factors in colorectal cancer (12 papers), Genetic and rare skin diseases. (9 papers) and Genetic Associations and Epidemiology (9 papers). The work is most often cited by research in Genetics (6.4k citations), Hematology (1.5k citations), Oncology (3.4k citations), Cancer Research (1.9k citations) and Genetics (1.1k citations). Mark H. Skolnick has collaborated with scholars based in United States, United Kingdom and Italy. Frequent co-authors include R. White, David Botstein, Ronald W. Davis, Alexander Kamb, Nelleke A. Gruis, Sean V. Tavtigian, D. Timothy Bishop, Jane Weaver-Feldhaus, Lisa Cannon‐Albright and Elisabeth Stockert. Their work appears in journals such as Genomics, Science, Cytogenetic and Genome Research, New England Journal of Medicine and Genetic Epidemiology.

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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