ScholarIQanswers from OpenAlex & ORCID
Tania Attié‐Bitach
ResearcherPublications, citations & collaboration network
Tania Attié‐Bitach is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Tania Attié‐Bitach have?
ScholarIQindexed works
Tania Attié‐Bitach has 313 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Tania Attié‐Bitach have?
ScholarIQcitation count
Tania Attié‐Bitach has 17,556 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Tania Attié‐Bitach?
ScholarIQh-index
Tania Attié‐Bitach has an h-index of 76 in OpenAlex.
What is the i10-index of Tania Attié‐Bitach?
ScholarIQi10-index
Tania Attié‐Bitach has an i10-index of 183 in OpenAlex.
What is the ORCID of Tania Attié‐Bitach?
ScholarIQorcid
The ORCID for Tania Attié‐Bitach is on the source record.
What is the OpenAlex record for Tania Attié‐Bitach?
ScholarIQopenalex
The OpenAlex for Tania Attié‐Bitach is on the source record.
What are the most-cited papers on Tania Attié‐Bitach?
ScholarIQmost cited works
The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome
Marion Delous, Lekbir Baala, Rémi Salomon, Christine Laclef, Jeanette Vierkotten, Kálmán Tory, Christelle Golzio, Tiphanie Lacoste, Laurianne Besse, Catherine Ozilou, Imane Moutkine, Nathan E. Hellman, Isabelle Anselme, Flora Silbermann, Christine Vesque, Christoph Gerhardt, Eleanor Rattenberry, Matthias T. F. Wolf, Marie-Claire Gübler, Jéléna Martinovic, Férechté Encha‐Razavi, Nathalie Boddaert, Marie Gonzalès, Marie Alice Macher, Hubert Nivet, Gérard Champion, Jean Pierre Berthélémé, Patrick Niaudet, Fiona McDonald, Friedhelm Hildebrandt, Colin A. Johnson, Michel Vekemans, Corinne Antignac, Ulrich Rüther, Sylvie Schneider‐Maunoury, Tania Attié‐Bitach, Sophie Saunier
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum
NISC Comparative Sequencing Program, Erica E. Davis, Qi Zhang, Qin Liu, Bill H. Diplas, Lisa Davey, Jane Hartley, Corinne Stoetzel, Katarzyna Szymańska, Gokul Ramaswami, Clare V. Logan, Donna M. Muzny, Alice Young, David A. Wheeler, Pedro Cruz, Margaret Morgan, Lora Lewis, Praveen F. Cherukuri, Baishali Maskeri, Nancy F. Hansen, James C. Mullikin, Robert W. Blakesley, Gerard G. Bouffard, Gàbor Gyapay, Susanne Rieger, Burkhard Tönshoff, Ilse Kern, Neveen A. Soliman, Thomas J. Neuhaus, Kathryn J. Swoboda, Hülya Kayserili, Tomas E Gallagher, Richard A. Lewis, Carsten Bergmann, Edgar A. Otto, Sophie Saunier, Peter Scambler, Philip L. Beales, Joseph G. Gleeson, Eamonn R. Maher, Tania Attié‐Bitach, Hélène Dollfus, Colin A. Johnson, Eric D. Green, Richard A. Gibbs, Friedhelm Hildebrandt, Eric A. Pierce, Nicholas Katsanis
A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies
Hemant Khanna, Erica E. Davis, Carlos Murga‐Zamalloa, Alejandro Estrada‐Cuzcano, Irma López, Anneke I. den Hollander, Marijke N. Zonneveld, Mohammad Othman, Naushin Waseem, Christina Chakarova, C. Maubaret, Anna Dı́az-Font, Ian M. MacDonald, Donna M. Muzny, David A. Wheeler, Margaret Morgan, Lora Lewis, Clare V. Logan, Perciliz L. Tan, M Beer, Chris F. Inglehearn, Richard A. Lewis, Samuel G. Jacobson, Carsten Bergmann, Philip L. Beales, Tania Attié‐Bitach, Colin A. Johnson, Edgar A. Otto, Shomi S. Bhattacharya, Friedhelm Hildebrandt, Richard A. Gibbs, Robert K. Koenekoop, Anand Swaroop, Nicholas Katsanis