Herbert A. Lubs

10.3k total citations · 1 hit paper
141 papers, 6.8k citations indexed

About

Herbert A. Lubs is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Herbert A. Lubs has authored 141 papers receiving a total of 6.8k indexed citations (citations by other indexed papers that have themselves been cited), including 79 papers in Genetics, 63 papers in Molecular Biology and 17 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Herbert A. Lubs's work include Genetics and Neurodevelopmental Disorders (44 papers), Genomic variations and chromosomal abnormalities (32 papers) and Chromosomal and Genetic Variations (16 papers). Herbert A. Lubs is often cited by papers focused on Genetics and Neurodevelopmental Disorders (44 papers), Genomic variations and chromosomal abnormalities (32 papers) and Chromosomal and Genetic Variations (16 papers). Herbert A. Lubs collaborates with scholars based in United States, Norway and Italy. Herbert A. Lubs's co-authors include Charles E. Schwartz, Ram S. Verma, Shivanand R. Patil, Roger E. Stevenson, Wendell H. McKenzie, William J. Kimberling, Bruce F. Pennington, Shelley D. Smith, Roger E. Stevenson and F.H. Ruddle and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Herbert A. Lubs

135 papers receiving 6.2k citations

Hit Papers

A marker X chromosome. 1969 2026 1988 2007 1969 100 200 300 400

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Herbert A. Lubs United States 46 3.5k 2.8k 1.2k 970 878 141 6.8k
William J. Kimberling United States 54 3.5k 1.0× 6.3k 2.3× 738 0.6× 921 0.9× 614 0.7× 186 11.6k
Roberto Giorda Italy 41 2.0k 0.6× 2.0k 0.7× 765 0.7× 552 0.6× 469 0.5× 157 5.1k
Judith L. Ross United States 59 5.9k 1.7× 4.3k 1.5× 1.4k 1.2× 1.4k 1.5× 259 0.3× 212 10.0k
Julie R. Korenberg United States 51 2.5k 0.7× 5.5k 1.9× 631 0.5× 919 0.9× 230 0.3× 167 10.5k
M. Anne Spence United States 44 2.9k 0.8× 1.6k 0.6× 302 0.3× 2.2k 2.3× 346 0.4× 157 6.3k
Wendy H. Raskind United States 50 1.6k 0.5× 3.2k 1.1× 203 0.2× 684 0.7× 1.4k 1.6× 144 8.4k
Stephanie L. Sherman United States 55 6.8k 2.0× 4.2k 1.5× 2.2k 1.9× 3.6k 3.7× 295 0.3× 208 11.6k
Lisbeth Tranebjærg Denmark 43 2.3k 0.7× 3.6k 1.3× 468 0.4× 417 0.4× 147 0.2× 163 6.7k
Jane A. Hurst United Kingdom 34 3.1k 0.9× 2.6k 0.9× 447 0.4× 577 0.6× 648 0.7× 85 7.7k
Rita M. Cantor United States 45 3.4k 1.0× 2.8k 1.0× 188 0.2× 2.6k 2.7× 244 0.3× 90 7.2k

Countries citing papers authored by Herbert A. Lubs

Since Specialization
Citations

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

Fields of papers citing papers by Herbert A. Lubs

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Herbert A. Lubs. 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 Herbert A. Lubs. The network helps show where Herbert A. Lubs may publish in the future.

Co-authorship network of co-authors of Herbert A. Lubs

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

All Works

20 of 20 papers shown
1.
Lubs, Herbert A., et al.. (2012). Fragile X and X-Linked Intellectual Disability: Four Decades of Discovery. The American Journal of Human Genetics. 90(4). 579–590. 160 indexed citations
2.
Peters, W.H.M., et al.. (2009). Ketosis, Serum Carnitine and its Precursor Amino Acids in Normal and Diabetic Ethiopians. Experimental and Clinical Endocrinology & Diabetes. 90(4). 83–92.
3.
Ramser, Juliane, Fatima Abidi, Céline Burcklé, et al.. (2005). A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor. Human Molecular Genetics. 14(8). 1019–1027. 146 indexed citations
4.
Stocco, Rita de Cássia, Willy Beçak, C.J. Lindsey, et al.. (2003). Shashi XLMR syndrome: Report of a second family. American Journal of Medical Genetics Part A. 118A(1). 49–51. 8 indexed citations
5.
Plenge, Robert M., et al.. (2002). Skewed X-Chromosome Inactivation Is a Common Feature of X-Linked Mental Retardation Disorders. The American Journal of Human Genetics. 71(1). 168–173. 177 indexed citations
6.
Arena, J. Fernando, et al.. (1999). XLMR database. American Journal of Medical Genetics. 85(3). 202–205. 2 indexed citations
7.
Lubs, Herbert A., et al.. (1999). X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28. American Journal of Medical Genetics. 85(3). 236–242. 23 indexed citations
8.
Lubs, Herbert A., Fatima Abidi, Jo‐Ann Blaymore Bier, et al.. (1999). XLMR syndrome characterized by multiple respiratory infections, hypertelorism, severe CNS deterioration and early death localizes to distal Xq28. American Journal of Medical Genetics. 85(3). 243–248. 54 indexed citations
9.
Neri, Giovanni, Pietro Chiurazzi, J. Fernando Arena, & Herbert A. Lubs. (1994). XLMR genes: Update 1994. American Journal of Medical Genetics. 51(4). 542–549. 47 indexed citations
10.
Stevenson, Roger E., Charles E. Schwartz, J. Fernando Arena, & Herbert A. Lubs. (1994). X‐linked mental retardation: The early era from 1943 to 1969. American Journal of Medical Genetics. 51(4). 538–541. 4 indexed citations
11.
Lubs, Herbert A., Mark Rabin, Esther Feldman, et al.. (1993). Familial dyslexia: genetic and medical findings in eleven three-generation families. Annals of Dyslexia. 43(1). 44–60. 28 indexed citations
12.
Ledbetter, David H., Joe Leigh Simpson, Mitchell S. Golbus, et al.. (1992). Cytogenetic results from the U.S. collaborative study on CVS. Prenatal Diagnosis. 12(5). 317–345. 264 indexed citations
13.
Desnick, Robert J., Jane L. Schuette, Mitchell S. Golbus, et al.. (1992). First‐trimester biochemical and molecular diagnoses using chorionic villi: High accuracy in the U.S. collaborative study. Prenatal Diagnosis. 12(5). 357–372. 16 indexed citations
14.
Bialer, Martin G., Laura Lawrence, Roger E. Stevenson, et al.. (1992). Allan‐herndon‐dudley syndrome: Clinical and linkage studies on a second family. American Journal of Medical Genetics. 43(1-2). 491–497. 34 indexed citations
15.
Pennington, Bruce F., Linda L. McCabe, Shelley D. Smith, et al.. (1986). Spelling Errors in Adults with a Form of Familial Dyslexia. Child Development. 57(4). 1001–1001. 82 indexed citations
16.
Robinson, Arthur, Herbert A. Lubs, & Daniel Bergsma. (1979). Sex chromosome aneuploidy : prospective studies on children. 20 indexed citations
17.
Verma, Ram S. & Herbert A. Lubs. (1976). Inheritance of Acridine Orange R Variants in Human Acrocentric Chromosomes. Human Heredity. 26(4). 315–318. 21 indexed citations
18.
McKenzie, Wendell H. & Herbert A. Lubs. (1975). Human Q and C chromosomal variations: distribution and incidence. Cytogenetic and Genome Research. 14(2). 97–115. 141 indexed citations
19.
Verma, Ram S. & Herbert A. Lubs. (1975). A simple R banding technic.. PubMed. 27(1). 110–7. 120 indexed citations
20.
Lubs, Herbert A. & Frank H. Ruddle. (1973). A (14;22) Robertsonian translocation, 45 chromosomes. Cytogenetic and Genome Research. 12(5). 368–369. 2 indexed citations

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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