Ingo Kennerknecht

2.9k total citations
66 papers, 1.5k citations indexed

About

Ingo Kennerknecht is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Ingo Kennerknecht has authored 66 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Genetics, 25 papers in Molecular Biology and 19 papers in Cognitive Neuroscience. Recurrent topics in Ingo Kennerknecht's work include Genomic variations and chromosomal abnormalities (17 papers), Prenatal Screening and Diagnostics (15 papers) and Face Recognition and Perception (14 papers). Ingo Kennerknecht is often cited by papers focused on Genomic variations and chromosomal abnormalities (17 papers), Prenatal Screening and Diagnostics (15 papers) and Face Recognition and Perception (14 papers). Ingo Kennerknecht collaborates with scholars based in Germany, United States and Poland. Ingo Kennerknecht's co-authors include Gotthold Barbi, M. Grueter, Thomas Grueter, Jürgen Horst, Steve Edwards, Peter Steinbach, Virginia Wong, R. Terinde, Walther Vogel and Sabine Schwemmle and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Neurology.

In The Last Decade

Ingo Kennerknecht

64 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ingo Kennerknecht Germany 23 712 550 393 317 262 66 1.5k
Susana Camposano United States 14 529 0.7× 242 0.4× 230 0.6× 22 0.1× 125 0.5× 20 1.7k
Giovanna Pari Canada 16 378 0.5× 221 0.4× 297 0.8× 37 0.1× 47 0.2× 26 1.2k
Kristina Aldridge United States 21 193 0.3× 703 1.3× 396 1.0× 42 0.1× 29 0.1× 36 1.4k
Whitney E. Parker United States 12 163 0.2× 131 0.2× 230 0.6× 39 0.1× 30 0.1× 21 795
James N. Ver Hoeve United States 19 133 0.2× 226 0.4× 400 1.0× 14 0.0× 39 0.1× 57 1.1k
James B. Brewer United States 14 1.0k 1.4× 53 0.1× 171 0.4× 20 0.1× 81 0.3× 24 2.1k
Judith Schmitz Germany 20 727 1.0× 224 0.4× 523 1.3× 10 0.0× 170 0.6× 44 1.5k
David McDonald United Kingdom 15 394 0.6× 138 0.3× 252 0.6× 7 0.0× 40 0.2× 35 1.4k
Jennifer K. E. Steeves Canada 17 877 1.2× 60 0.1× 107 0.3× 125 0.4× 297 1.1× 68 1.1k
John Ostuni United States 18 273 0.4× 30 0.1× 88 0.2× 74 0.2× 157 0.6× 32 1.0k

Countries citing papers authored by Ingo Kennerknecht

Since Specialization
Citations

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

Fields of papers citing papers by Ingo Kennerknecht

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ingo Kennerknecht

This figure shows the co-authorship network connecting the top 25 collaborators of Ingo Kennerknecht. A scholar is included among the top collaborators of Ingo Kennerknecht 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 Ingo Kennerknecht. Ingo Kennerknecht 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.
Altunoğlu, Umut, Anju Shukla, Nathalie Escande‐Beillard, et al.. (2021). Expanding the spectrum of syndromic PPP2R3C ‐related XY gonadal dysgenesis to XX gonadal dysgenesis. Clinical Genetics. 101(2). 221–232. 5 indexed citations
2.
Guala, Andrea, et al.. (2017). Neoplasia in Cri du Chat Syndrome from Italian and German Databases. SHILAP Revista de lepidopterología. 2017. 1–3. 8 indexed citations
3.
Budde, Birgit, Shuji Mizumoto, Christian Becker, et al.. (2015). Skeletal dysplasia in a consanguineous clan from the island of Nias/Indonesia is caused by a novel mutation in B3GAT3. Human Genetics. 134(7). 691–704. 25 indexed citations
4.
Johnen, Andreas, et al.. (2014). A family at risk: Congenital prosopagnosia, poor face recognition and visuoperceptual deficits within one family. Neuropsychologia. 58. 52–63. 29 indexed citations
5.
Jost, Jürgen, et al.. (2011). Deficits in Long-Term Recognition Memory Reveal Dissociated Subtypes in Congenital Prosopagnosia. PLoS ONE. 6(1). e15702–e15702. 42 indexed citations
6.
Oven, Mannis van, M. Van Schoor, Geoff Kushnick, et al.. (2010). Unexpected Island Effects at an Extreme: Reduced Y Chromosome and Mitochondrial DNA Diversity in Nias. Molecular Biology and Evolution. 28(4). 1349–1361. 35 indexed citations
7.
Toddenroth, Dennis, Martin Dugas, & Ingo Kennerknecht. (2010). Sorting chromosomes as a software‐based exercise. Medical Education. 44(11). 1127–1127. 1 indexed citations
8.
Dinkelacker, Vera, Martina Grüter, Peter Klaver, et al.. (2010). Congenital prosopagnosia: multistage anatomical and functional deficits in face processing circuitry. Journal of Neurology. 258(5). 770–782. 49 indexed citations
9.
Kennerknecht, Ingo. (2007). Congenital prosopagnosia - a common hereditary cognitive dysfunction in humans. Frontiers in bioscience. 13(13). 3150–3150. 25 indexed citations
10.
Kennerknecht, Ingo, et al.. (2006). First report of prevalence of non‐syndromic hereditary prosopagnosia (HPA). American Journal of Medical Genetics Part A. 140A(15). 1617–1622. 188 indexed citations
11.
Pusch, Carsten M., Martina Broghammer, Graeme Nicholson, et al.. (2004). PCR-Induced Sequence Alterations Hamper the Typing of Prehistoric Bone Samples for Diagnostic Achondroplasia Mutations. Molecular Biology and Evolution. 21(11). 2005–2011. 18 indexed citations
12.
Barbi, Gotthold, et al.. (2000). Mirror-symmetric duplicated chromosome 21q with minor proximal deletion, and with neocentromere in a child without the classical Down syndrome phenotype. American Journal of Medical Genetics. 91(2). 116–122. 12 indexed citations
13.
Kennerknecht, Ingo, Rolf E. Brenner, Walter Just, et al.. (1995). Agonadism in two sisters with XY gonosomal constitution, mental retardation, short stature, severely retarded bone age, and multiple extragenital malformations: A new autosomal recessive syndrome. American Journal of Medical Genetics. 59(1). 62–67. 13 indexed citations
14.
Kellner, James D., F. Strian, Klaus Faßbender, Ingo Kennerknecht, & Ronald Klein. (1994). DIDMOAD (Wolfram) syndrome [Letter]. The British Journal of Psychiatry. 164. 132–132. 1 indexed citations
15.
Kennerknecht, Ingo, Sabine Krämer, Dieter Grab, R. Terinde, & Walther Vogel. (1993). A prospective cytogenetic study of third‐trimester placentae in small‐for‐date but otherwise normal newborns. Prenatal Diagnosis. 13(4). 257–269. 17 indexed citations
16.
Steinbach, Peter, Gholamali Tariverdian, Ingo Kennerknecht, et al.. (1993). Molecular analysis of mutations in the gene FMR-1 segregating in fragile X families. Human Genetics. 92(5). 491–498. 12 indexed citations
17.
Kennerknecht, Ingo, et al.. (1992). Nuclear and chromosomal replication patterns in chorionic villi cells by bromodeoxyuridine labelling and DNA flow cytometry. Cell Proliferation. 25(4). 321–336. 3 indexed citations
18.
Kennerknecht, Ingo, et al.. (1991). Proliferation kinetics in native chorionic villus cells. Prenatal Diagnosis. 11(8). 591–595. 1 indexed citations
19.
20.
Kennerknecht, Ingo, Gotthold Barbi, & Walther Vogel. (1990). Maternal transmission of ring chromosome 21. Human Genetics. 86(1). 99–101. 14 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Susana Camposano Breakdown of academic impact, for papers by Giovanna Pari Breakdown of academic impact, for papers by Kristina Aldridge Breakdown of academic impact, for papers by Whitney E. Parker Breakdown of academic impact, for papers by James N. Ver Hoeve Breakdown of academic impact, for papers by James B. Brewer Breakdown of academic impact, for papers by Judith Schmitz Breakdown of academic impact, for papers by David McDonald Breakdown of academic impact, for papers by Jennifer K. E. Steeves Breakdown of academic impact, for papers by John Ostuni
Rankless by CCL
2026