Mark Leppert

14.7k total citations · 2 hit papers
63 papers, 5.9k citations indexed

About

Mark Leppert is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Mark Leppert has authored 63 papers receiving a total of 5.9k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 24 papers in Genetics and 8 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Mark Leppert's work include Genomic variations and chromosomal abnormalities (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Mark Leppert is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Mark Leppert collaborates with scholars based in United States, Poland and Canada. Mark Leppert's co-authors include Mark Keating, G. Michael Vincent, Katherine W. Timothy, Donald L. Atkinson, Colleen A. Morris, Mark T. Keating, A.D. Stock, Keith L. Sternes, Patricia Spallone and Andy Peiffer and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Mark Leppert

63 papers receiving 5.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

1998 939 citations Dora Stauffer, Andy Peiffer et al. Nature Genetics profile →
Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome

1993 809 citations Mark Leppert et al. Nature Genetics profile →

Peers

Countries citing papers authored by Mark Leppert

Since Specialization

Citations

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

Fields of papers citing papers by Mark Leppert

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mark Leppert

This figure shows the co-authorship network connecting the top 25 collaborators of Mark Leppert. A scholar is included among the top collaborators of Mark Leppert 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 Mark Leppert. Mark Leppert is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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

20 of 20 papers shown

#	Work	Indexed citations
1	Detection and editing of the updated Arabidopsis plastid- and mitochondrial-encoded proteomes through PeptideAtlas 2023 ·PLANT PHYSIOLOGY ·Klaas J. van Wijk, Stéphane Bentolila, Mark Leppert, Qi Sun, Zhi Sun, Luis Mendoza, (unknown), Eric W. Deutsch	6
2	The Arabidopsis PeptideAtlas: Harnessing worldwide proteomics data to create a comprehensive community proteomics resource 2021 ·The Plant Cell ·Klaas J. van Wijk, Mark Leppert, Qi Sun, (unknown), Zhi Sun, Luis Mendoza, Eric W. Deutsch	40
3	A family‐based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic hernia 2012 ·American Journal of Medical Genetics Part A ·Cammon B. Arrington, Steven B. Bleyl, Nori Matsunami, Neil E. Bowles, Mark Leppert, Bradley L. Demarest, Karen A. Osborne, Bradley A. Yoder, Janice L. B. Byrne, Joshua D. Schiffman, Donald M. Null, Robert DiGeronimo, Michael D. Rollins, Roger G. Faix, Jessica Comstock, Nicola J. Camp, Mark Leppert, H. Joseph Yost, Luca Brunelli	22
4	Colorectal adenomas and cancer link to chromosome 13q22.1–13q31.3 in a large family with excess colorectal cancer 2010 ·Journal of Medical Genetics ·Deborah W. Neklason, Thérèse M.F. Tuohy, Jeffrey Stevens, (unknown), Lisa Baird, Richard A. Kerber, Wade S. Samowitz, Scott K. Kuwada, Mark Leppert, R. Burt	13
5	Associations between phenylthiocarbamide gene polymorphisms and cigarette smoking 2005 ·Nicotine & Tobacco Research ·Dale S. Cannon, Timothy R. Baker, Megan E. Piper, Mary Beth Scholand, (unknown), Dennis Drayna, William McMahon, (unknown), (unknown), Hilary Coon, Mark Leppert	72
6	A longitudinal study of X-inactivation ratio in human females 2004 ·Human Genetics ·Ionel Sandovici, Anna K. Naumova, Mark Leppert, (unknown), Carmen Sapienza	53
7	Further Evidence for the Role of Genes on Chromosome 2 and Chromosome 5 in the Inheritance of Pulmonary Function 2003 ·American Journal of Respiratory and Critical Care Medicine ·Alka Malhotra, Andy Peiffer, (unknown), Tami Elsner, Richard E. Kanner, Mark Leppert, Sandra J. Hasstedt	30
8	Future Research Directions in Acute Lung Injury: Summary of a National Heart, Lung, and Blood Institute Working Group 2003 ·American Journal of Respiratory and Critical Care Medicine ·Michael A. Matthay, Guy A. Zimmerman, Charles Esmon, Jahar Bhattacharya, Barry S. Coller, Claire M. Doerschuk, Joanna Floros, Michael A. Gimbrone, Eric P. Hoffman, Rolf D. Hubmayr, Mark Leppert, Sadis Matalon, Robert S. Munford, Polly E. Parsons, Arthur S. Slutsky, Kevin J. Tracey, Peter A. Ward, Dorothy B. Gail, Andrea L. Harabin	411
9	Genetic analysis of a complex trait in the Utah Genetic Reference Project: a major locus for PTC taste ability on chromosome 7q and a secondary locus on chromosome 16p 2003 ·Human Genetics ·Dennis Drayna, Hilary Coon, Un‐Kyung Kim, Tami Elsner, (unknown), Brith Otterud, Lisa Baird, Andy Peiffer, Mark Leppert	112
10	Common variant of human NEDD4L activates a cryptic splice site to form a frameshifted transcript 2002 ·Journal of Human Genetics ·Diane M. Dunn, Tomoaki Ishigami, James S. Pankow, Andrew von Niederhausern, Jonathan K. Alder, Steven C. Hunt, Mark Leppert, J.-M. Lalouel, Robert B. Weiss	66
11	ILAE Genetics Commission Conference Report: Molecular Analysis of Complex Genetic Epilepsies 2002 ·Epilepsia ·(unknown), Eric C. Anderson, Samuel F. Berkovic, Olivier Dulac, (unknown), Sanjeev Jain, (unknown), Dick Lindhout, Jeffrey L. Noebels, Ruth Ottman, A. Scaramelli, José M. Serratosa, Ortrud K. Steinlein, G. Avanzini, Joan E. Bailey‐Wilson, Lon R. Cardon, Roman Fischbach, (unknown), Mark Leppert, Jürg Ott, Kerstin Lindblad‐Toh, (unknown)	17
12	Novel K⁺ Channel Genes in Benign Familial Neonatal Convulsions 2000 ·Epilepsia ·Mark Leppert	3
13	The rod photoreceptor ATP-binding cassette transporter gene, ABCR, and retinal disease: from monogenic to multifactorial 1999 ·Vision Research ·Noah F. Shroyer, Richard A. Lewis, Rando Allikmets, Nanda Singh, Michael Dean, Mark Leppert, James R. Lupski	94
14	Genetic mapping of X-linked loci involved in skewing of X chromosome inactivation in the human 1998 ·European Journal of Human Genetics ·Anna K. Naumova, (unknown), Lynne M. Bird, Mark A. Smith, (unknown), Mark Leppert, Kenneth Morgan, Carmen Sapienza	60
15	Genetic Heterogeneity in Familial Acute Myelogenous Leukemia: Evidence for a Second Locus at Chromosome 16q21-23.2 1997 ·The American Journal of Human Genetics ·Marshall S. Horwitz, Kathleen F. Benson, (unknown), John Wolff, Mark Leppert, Lynne Hobson, Marie Mangelsdorf, Sui Yu, D. Hewett, Robert I. Richards, Wendy H. Raskind	32
16	Genetic mapping of adrenergic receptor genes in humans 1995 ·Journal of Molecular Medicine ·(unknown), Brith Otterud, Wen‐Tsong Hsieh, María Martínez, Dora Stauffer, John Holik, Wade H. Berrettini, William Byerley, (unknown), J.-M. Lalouel, Mark Leppert	22
17	Coancestry in Apparently Sporadic Primary Pulmonary Hypertension 1995 ·CHEST Journal ·Greg Elliott, (unknown), Mark Leppert, (unknown), Richard A. Kerber	19
18	Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3p 1995 ·Nature Genetics ·Launce Gouw, Craig D. Kaplan, (unknown), Kathleen B. Digre, S. Lane Rutledge, Antoni Matilla‐Dueñas, Mark Leppert, Huda Y. Zoghbi, Louis J. Ptáček	110
19	Discordance of the T‐cell receptor alpha‐chain gene in familial multiple sclerosis 1992 ·Neurology ·Sharon Lynch, John Rose, Jack H. Petajan, Mark Leppert	29
20	Isolation and mapping of a polymorphic DNA sequence pHB159 on chromosome 11 [D11S146] 1988 ·Nucleic Acids Research ·Yusuke Nakamura, (unknown), P. O’Connell, Mark Leppert, G.M. Lathrop, J.-M. Lalouel, R. White	8

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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