Lorraine Suslak

407 citations
14 papers · 290 indexed · h-index 9
Topics
Prenatal Screening and Diagnostics (4 papers)Genomic variations and chromosomal abnormalities (4 papers)Genetic Syndromes and Imprinting (3 papers)
Partner nations
United StatesSwitzerland

In The Last Decade

Lorraine Suslak

14 papers receiving 282 citations

Peers

Lorraine Suslak
Comparison fields: 5 of 43
  • Genetics 231
  • Pediatrics, Perinatology and Child Health 159
  • Molecular Biology 90
  • Plant Science 33
  • Clinical Psychology 13
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Countries citing papers authored by Lorraine Suslak

Since Specialization
Citations

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

Fields of papers citing papers by Lorraine Suslak

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lorraine Suslak

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

All Works

14 of 14 papers shown
#WorkIndexed citations
1 10
2 55
3 7
4
Paternal isodisomy for chromosome 5 in a child with spinal muscular atrophy.
36
5 88
6
Crouzon syndrome: prenatal ultrasound diagnosis by binocular diameters.
13
7 3
8 5
9 22
10
Crouzon syndrome with periapical cemental dysplasia and acanthosis nigricans: the pleiotropic effect of a single gene?
16
11 14
12 4
13 11
14 6

About Lorraine Suslak

Lorraine Suslak is a scholar working on Anatomy, Genetics and Pediatrics, Perinatology and Child Health, having authored 14 papers that have together received 290 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic Syndromes and Imprinting (3 papers). The work is most often cited by research in Genetics (231 citations), Pediatrics, Perinatology and Child Health (159 citations) and Developmental Biology (8 citations). Lorraine Suslak has collaborated with scholars based in United States and Switzerland. Frequent co-authors include Hana Aviv, Franklin Desposito, Fosco Bernasconi, C Baccichetti, Wendy P. Robinson, Ling-Yu Shih, Emilio Franzonı, John Wagstaff, Lina Artifoni and Albert Schinzel. Their work appears in journals such as Journal of Medical Genetics, American Journal of Medical Genetics and Prenatal Diagnosis.

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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