Ralph S. Lachman

8.9k total citations
181 papers, 5.5k citations indexed

About

Ralph S. Lachman is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Ralph S. Lachman has authored 181 papers receiving a total of 5.5k indexed citations (citations by other indexed papers that have themselves been cited), including 113 papers in Genetics, 65 papers in Molecular Biology and 42 papers in Oncology. Recurrent topics in Ralph S. Lachman's work include Connective tissue disorders research (82 papers), Bone health and treatments (39 papers) and Bone Metabolism and Diseases (17 papers). Ralph S. Lachman is often cited by papers focused on Connective tissue disorders research (82 papers), Bone health and treatments (39 papers) and Bone Metabolism and Diseases (17 papers). Ralph S. Lachman collaborates with scholars based in United States, Canada and Germany. Ralph S. Lachman's co-authors include David L. Rimoin, Daniel H. Cohn, Deborah Krakow, William R. Wilcox, Hooshang Taybi, David F. Merten, Leslie M. Thompson, Patricia L. Tavormina, John J. Wasmuth and Geert Mortier and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and Nature Genetics.

In The Last Decade

Ralph S. Lachman

177 papers receiving 5.3k citations

Peers

Ralph S. Lachman
Jürgen W. Spranger Germany
Deborah Krakow United States
Gen Nishimura Japan
Jacky Bonaventure France
Yasuteru Muragaki Japan
Vesa Kaartinen United States
Rosa Serra United States
Hiromi Yanagisawa United States
Marina Colombi Italy
Beate Lanske United States
Jürgen W. Spranger Germany
Ralph S. Lachman
Citations per year, relative to Ralph S. Lachman Ralph S. Lachman (= 1×) peers Jürgen W. Spranger

Countries citing papers authored by Ralph S. Lachman

Since Specialization
Citations

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

Fields of papers citing papers by Ralph S. Lachman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ralph S. Lachman. 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 Ralph S. Lachman. The network helps show where Ralph S. Lachman may publish in the future.

Co-authorship network of co-authors of Ralph S. Lachman

This figure shows the co-authorship network connecting the top 25 collaborators of Ralph S. Lachman. A scholar is included among the top collaborators of Ralph S. Lachman 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 Ralph S. Lachman. Ralph S. Lachman 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.
Pettersson, Maria, Dora Dias‐Santagata, Daniel Nilsson, et al.. (2023). Case report: Extending the spectrum of clinical and molecular findings in FOXC1 haploinsufficiency syndrome. Frontiers in Genetics. 14. 1174046–1174046. 5 indexed citations
2.
Zhang, Wenjuan, S. Paige Taylor, Iván Durán, et al.. (2017). Expanding the genetic architecture and phenotypic spectrum in the skeletal ciliopathies. Human Mutation. 39(1). 152–166. 83 indexed citations
3.
Alanay, Yasemin & Ralph S. Lachman. (2011). A Review of the Principles of Radiological Assessment of Skeletal Dysplasias. Journal of Clinical Research in Pediatric Endocrinology. 3(4). 163–178. 40 indexed citations
4.
Krakow, Deborah, Joris Vriens, Natalia Camacho, et al.. (2009). Mutations in the Gene Encoding the Calcium-Permeable Ion Channel TRPV4 Produce Spondylometaphyseal Dysplasia, Kozlowski Type and Metatropic Dysplasia. The American Journal of Human Genetics. 84(3). 307–315. 148 indexed citations
5.
Tompson, Stuart W., Barry Merriman, Vincent Funari, et al.. (2008). A Recessive Skeletal Dysplasia, SEMD Aggrecan Type, Results from a Missense Mutation Affecting the C-Type Lectin Domain of Aggrecan. The American Journal of Human Genetics. 84(1). 72–79. 101 indexed citations
6.
Rimoin, David L., Daniel H. Cohn, Deborah Krakow, et al.. (2007). The Skeletal Dysplasias. Annals of the New York Academy of Sciences. 1117(1). 302–309. 47 indexed citations
7.
Elliott, Alison M., William R. Wilcox, Gerald S. Spear, et al.. (2006). Osteocraniostenosis–hypomineralized skull with gracile long bones and splenic hypoplasia. Four new cases with distinctive chondro‐osseous morphology. American Journal of Medical Genetics Part A. 140A(14). 1553–1563. 8 indexed citations
8.
Elliott, Alison M., et al.. (2004). Hand involvement in Schmid metaphyseal chondrodysplasia. American Journal of Medical Genetics Part A. 132A(2). 191–193. 9 indexed citations
9.
Lee, Yung Seng, et al.. (2003). A distinctive type of metaphyseal chondrodysplasia with characteristic thickening of the distal ulna and radius: Possible metaphyseal chondrodysplasia‐rosenberg. American Journal of Medical Genetics Part A. 119A(1). 50–56. 1 indexed citations
10.
Unger, Sheila, Michael D. Briggs, Paul Holden, et al.. (2001). Multiple epiphyseal dysplasia: radiographic abnormalities correlated with genotype. Pediatric Radiology. 31(1). 10–18. 41 indexed citations
11.
Quadrelli, Roberto, Alicia Vaglio, Aída Lemes, et al.. (2000). Uruguay facio-cardio-musculo-skeletal syndrome: A novel X-linked recessive disorder. American Journal of Medical Genetics. 95(3). 247–265. 1 indexed citations
12.
Berdon, W. E., et al.. (1997). Lumbar gibbus in storage diseases and bone dysplasias. Pediatric Radiology. 27(4). 289–294. 29 indexed citations
13.
Briggs, Michael D., Susan M.G. Hoffman, Lily King, et al.. (1995). Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene. Nature Genetics. 10(3). 330–336. 395 indexed citations
14.
Peeden, Joseph, et al.. (1992). Spondylometaphyseal dysplasia, sedaghatian type. American Journal of Medical Genetics. 44(5). 651–656. 12 indexed citations
15.
Dickman, Paul S., et al.. (1987). Bridging Bronchus and Posterior Left Pulmonary Artery. Pediatric Pathology. 7(5-6). 637–643. 8 indexed citations
16.
Burton, Barbara K., Thomas E. Sumner, Leonard O. Langer, et al.. (1986). A new skeletal dysplasia: Clinical, radiologic, and pathologic findings. The Journal of Pediatrics. 109(4). 642–648. 10 indexed citations
17.
Rimoin, David L., et al.. (1983). A distinct chondrodysplasia resembling Kniest dysplasia: Clinical, roentgenographic, histologic, and ultrastructural findings. The Journal of Pediatrics. 103(6). 898–904. 4 indexed citations
18.
Horton, William A., David L. Rimoin, Ralph S. Lachman, et al.. (1978). The phenotypic variability of diastrophic dysplasia. The Journal of Pediatrics. 93(4). 609–613. 51 indexed citations
19.
Thibeault, Donald W., et al.. (1975). Patent ductus arteriosus complicating the respiratory distress syndrome in preterm infants. The Journal of Pediatrics. 86(1). 120–126. 116 indexed citations
20.
Hollister, David W., et al.. (1973). The lacrimo-auriculo-dento-digital syndrome. The Journal of Pediatrics. 83(3). 438–444. 83 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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